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Cyclic nucleotide
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A cyclic nucleotide (cNMP) is a single-phosphate nucleotide with a cyclic bond arrangement between the sugar and phosphate groups. Like other nucleotides, cyclic nucleotides are composed of three functional groups: a sugar, a nitrogenous base, and a single phosphate group. As can be seen in the cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) images, the 'cyclic' portion consists of two bonds between the phosphate group and the 3' and 5' hydroxyl groups of the sugar, very often a ribose.
Their biological significance includes a broad range of protein-ligand interactions. They have been identified as secondary messengers in both hormone and ion-channel signalling in eukaryotic cells, as well as allosteric effector compounds of DNA binding proteins in prokaryotic cells. cAMP and cGMP are currently the most well documented cyclic nucleotides, however there is evidence that cCMP (with cytosine) is also involved in eukaryotic cellular messaging. The role of cyclic uridine monophosphate (cUMP) is even less well known.
Discovery of cyclic nucleotides has contributed greatly to the understanding of kinase and phosphatase mechanisms, as well as protein regulation in general. Although more than 50 years have passed since their initial discovery, interest in cyclic nucleotides and their biochemical and physiological significance continues.
History
[edit]The understanding of the concept of second messengers, and in particular the role of cyclic nucleotides and their ability to relay physiological signals to a cell, has its origins in the research of glycogen metabolism by Carl and Gerty Cori, for which they were awarded a Nobel Prize in Physiology or Medicine in 1947.[1] A number of incremental but important discoveries through the 1950s added to their research, primarily focusing on the activity of glycogen phosphorylase in dog liver. Glycogen phosphorylase catalyzes the first step in glycogenolysis, the process of breaking glycogen into its substituent glucose parts.[2] Earl Sutherland investigated the effect of the hormones adrenaline and glucagon on glycogen phosphorylase, earning him the Nobel Prize in Physiology or Medicine in 1971.[1]
In 1956 Edwin Krebs and Edmond Fischer discovered that adenosine triphosphate (ATP) is required for the conversion of glycogen phosphorylase b to glycogen phosphorylase a. While investigating the action of adrenaline on glycogenolysis the next year, Sutherland and Walter Wosilait reported that inorganic phosphate is released when the enzyme liver phosphorylase is inactivated; but when it is activated, it incorporates a phosphate.[1] The "active factor" that the hormones produced[2] was finally purified in 1958, and then identified as containing a ribose, a phosphate, and an adenine in equal ratios. Further, it was proved that this factor reverted to 5'-AMP when it was inactivated.[1]
Evgeny Fesenko, Stanislav Kolesnikov, and Arkady Lyubarsky discovered in 1985 that cyclic guanosine monophosphate (cGMP) can initiate the photoresponse in rods. Soon after, the role of cNMP in gated ion channels of chemosensitive cilia of olfactory sensory neurons was reported by Tadashi Nakamura and Geoffrey Gold. In 1992 Lawrence Haynes and King-Wai Yau uncovered cNMP's role in the light-dependent cyclic-nucleotide-gated channel of cone photoreceptors.[3] By the end of the decade, the presence of two types of intramembrane receptors was understood: Rs (which stimulates cyclase) and Ri (which inhibits cyclase). Wei-Jen Tang and James Hurley reported in 1998 that adenylyl cyclase, which synthesizes cAMP, is regulated not only by hormones and neurotransmitters, but also by phosphorylation, calcium, forskolin, and guanine nucleotide-binding proteins (G proteins).[2]
Chemistry of cNMPs
[edit]Structure
[edit]
The two most well-studied cyclic nucleotides are cyclic AMP (cAMP) and cyclic GMP (cGMP), while cyclic CMP (cCMP) and cyclic UMP (cUMP) are less understood. cAMP is 3'5'-cyclic adenosine monophosphate, cGMP is 3'5'-cyclic guanosine monophosphate, cCMP is cytidine 3',5'-monophosphate, and cUMP is uridine 3',5'-cyclic phosphate.[4][5]
Each cyclic nucleotide has three components. It contains a nitrogenous base (meaning it contains nitrogen): for example, adenine in cAMP and guanine in cGMP. It also contains a sugar, specifically the five-carbon ribose. And finally, a cyclic nucleotide contains a phosphate. A double-ring purine is the nitrogenous base for cAMP and cGMP, while cytosine, thymine, and uracil each have a single-ring nitrogenous base (pyrimidine).
These three components are connected so that the nitrogenous base is attached to the first carbon of ribose (1' carbon), and the phosphate group is attached to the 5' carbon of ribose. While all nucleotides have this structure, the phosphate group makes a second connection to the ribose ring at the 3' carbon in cyclic nucleotides. Because the phosphate group has two separate bonds to the ribose sugar, it forms a cyclic ring.[6]
The atom numbering convention is used to identify the carbons and nitrogens within a cyclic nucleotide. In the pentose, the carbon closest to the carbonyl group is labeled C-1. When a pentose is connected to a nitrogenous base, carbon atom numbering is distinguished with a prime (') notation, which differentiates these carbons from the atom numbering of the nitrogenous base.[7]
Therefore, for cAMP, 3'5'-cyclic adenosine monophosphate indicates that a single phosphate group forms a cyclic structure with the ribose group at its 3' and 5' carbons, while the ribose group is also attached to adenosine (this bond is understood to be at the 1' position of the ribose).
Biochemistry
[edit]Cyclic nucleotides are found in both prokaryotic and eukaryotic cells. Control of intracellular concentrations is maintained through a series of enzymatic reactions involving several families of proteins. In higher order mammals, cNMPs are present in many types of tissue.
Synthesis and Degradation
[edit]
Cyclic nucleotides are produced from the generic reaction NTP → cNMP + PPi,[8] where N represents a nitrogenous base. The reaction is catalyzed by specific nucleotidyl cyclases, such that production of cAMP is catalyzed by adenylyl cyclase and production of cGMP is catalyzed by guanylyl cyclase.[2] Adenylyl cyclase has been found in both a transmembrane and cytosolic form, representing distinct protein classes and different sources of cAMP.[9]
Both cAMP and cGMP are degraded by hydrolysis of the 3' phosphodiester bond, resulting in a 5'NMP. Degradation is carried out primarily by a class of enzymes known as phosphodiesterases (PDEs). In mammalian cells, there are 11 known PDE families with varying isoforms of each protein expressed based on the cell's regulatory needs. Some phosphodiesterases are cNMP-specific, while others can hydrolyze non-specifically.[10] However, the cAMP and cGMP degradation pathways are much more understood than those for either cCMP or cUMP. The identification of specific PDEs for cCMP and cUMP has not been as thoroughly established.[11]
Target Binding
[edit]Cyclic nucleotides can be found in many different types of eukaryotic cells, including photo-receptor rods and cones, smooth muscle cells and liver cells. Cellular concentrations of cyclic nucleotides can be very low, in the 10−7M range, because metabolism and function are often localized in particular parts of the cell.[1] A highly conserved cyclic nucleotide-binding domain (CNB) is present in all proteins that bind cNMPs, regardless of their biological function. The domain consists of a beta sandwich architecture, with the cyclic nucleotide binding pocket between the beta sheets. The binding of cNMP causes a conformational change that affects the protein's activity.[12] There is also data to support a synergistic binding effect amongst multiple cyclic nucleotides, with cCMP lowering the effective concentration (EC50) of cAMP for activation of protein kinase A (PKA).[13]
Biology
[edit]Cyclic nucleotides are integral to a communication system that acts within cells.[1] They act as "second messengers" by relaying the signals of many first messengers, such as hormones and neurotransmitters, to their physiological destinations. Cyclic nucleotides participate in many physiological responses,[14] including receptor-effector coupling, down-regulation of drug responsiveness, protein-kinase cascades, and transmembrane signal transduction.[1]
Cyclic nucleotides act as second messengers when first messengers, which cannot enter the cell, instead bind to receptors in the cellular membrane. The receptor changes conformation and transmits a signal that activates an enzyme in the cell membrane interior called adenylyl cyclase. This releases cAMP into the cell interior, where it stimulates a protein kinase called cyclic AMP-dependent protein kinase. By phosphorylating proteins, cyclic AMP-dependent protein kinase alters protein activity. cAMP's role in this process terminates upon hydrolysis to AMP by phosphodiesterase.[2]
| Cyclic nucleotide | Known binding proteins | Pathway/Biological association |
|---|---|---|
| cAMP |
|
|
| cGMP |
|
|
| cCMP |
|
Cyclic nucleotides are well-suited to act as second messengers for several reasons. Their synthesis is energetically favorable, and they are derived from common metabolic components (ATP and GTP). When they break down into AMP/GMP and inorganic phosphate, these components are non-toxic.[14] Finally, cyclic nucleotides can be distinguished from non-cyclic nucleotides because they are smaller and less polar.[2]
Biological significance
[edit]The involvement of cyclic nucleotides on biological functions is varied, while an understanding of their role continues to grow. There are several examples of their biological influence. They are associated with long-term and short-term memory.[20] They also work in the liver to coordinate various enzymes that control blood glucose and other nutrients.[21] In bacteria, cyclic nucleotides bind to catabolite gene activator protein (CAP), which acts to increase metabolic enzymatic activity by increasing the rate of DNA transcription.[5] They also facilitate relaxation of smooth muscle cells in vascular tissue,[22] and activate cyclic CNG channels in retinal photoreceptors and olfactory sensory neurons. In addition, they potentially activate cyclic CNG channels in: pineal gland light sensitivity, sensory neurons of the vomeronasal organ (which is involved in the detection of pheromones), taste receptor cells, cellular signaling in sperm, airway epithelial cells, gonadotropin-releasing hormone (GnRH)-secreting neuronal cell line, and renal inner medullary collecting duct.[3]
Pathway mutations and related diseases
[edit]Examples of disruptions of cNMP pathways include: mutations in CNG channel genes are associated with degeneration of the retina and with color blindness;[3] and overexpression of cytosolic or soluble adenylyl cyclase (sAC) has been linked to human prostate carcinoma. Inhibition of sAC, or knockdown by RNA interference (RNAi) transfection has been shown to prevent the proliferation of the prostate carcinoma cells. The regulatory pathway appears to be part of the EPAC pathway and not the PKA pathway.[9]
Phosphodiesterases, principle regulators of cNMP degradation, are often targets for therapeutics. Caffeine is a known PDE inhibitor, while drugs used for the treatment of erectile dysfunction like sildenafil and tadalafil also act through inhibiting the activity of phosphodiesterases.[10]
References
[edit]- ^ a b c d e f g Beavo JA, Brunton LL (September 2002). "Cyclic nucleotide research -- still expanding after half a century". Nat. Rev. Mol. Cell Biol. 3 (9): 710–8. doi:10.1038/nrm911. PMID 12209131. S2CID 33021271.
- ^ a b c d e f Newton RP, Smith CJ (September 2004). "Cyclic nucleotides". Phytochemistry. 65 (17): 2423–37. doi:10.1016/j.phytochem.2004.07.026. PMID 15381406.
- ^ a b c d e Kaupp UB, Seifert R (July 2002). "Cyclic nucleotide-gated ion channels". Physiol. Rev. 82 (3): 769–824. CiteSeerX 10.1.1.319.7608. doi:10.1152/physrev.00008.2002. PMID 12087135.
- ^ Seifert, R. (2015). "cCMP and cUMP: emerging second messengers". Trends in Biochemical Sciences. 40 (1): 8–15. doi:10.1016/j.tibs.2014.10.008. PMID 25435399.
- ^ a b Gomelsky, Mark (2011). "cAMP, c-di-GMP, c-di-AMP, and now cGMP: bacteria use them all!". Molecular Microbiology. 79 (3): 562–565. doi:10.1111/j.1365-2958.2010.07514.x. PMC 3079424. PMID 21255104.
- ^ Nelson, David; Michael Cox (2008). Lehninger Principles of Biochemistry (Fifth ed.). New York, NY: W.H. Freeman and Company. ISBN 978-0-7167-7108-1.
- ^ "Nucleotide Numbering". Tulane University. Retrieved 9 May 2013.
- ^ "National Library of Medicine - Medical Subject Headings, Adenylyl Cyclase".
- ^ a b Flacke JP, Flacke H, Appukuttan A, et al. (February 2013). "Type 10 soluble adenylyl cyclase is overexpressed in prostate carcinoma and controls proliferation of prostate cancer cells". J. Biol. Chem. 288 (5): 3126–35. doi:10.1074/jbc.M112.403279. PMC 3561535. PMID 23255611.
- ^ a b Bender AT, Beavo JA (September 2006). "Cyclic nucleotide phosphodiesterases: molecular regulation to clinical use". Pharmacol. Rev. 58 (3): 488–520. doi:10.1124/pr.58.3.5. PMID 16968949. S2CID 7397281.
- ^ Reinecke D, Schwede F, Genieser HG, Seifert R (2013). "Analysis of substrate specificity and kinetics of cyclic nucleotide phosphodiesterases with N'-methylanthraniloyl-substituted purine and pyrimidine 3',5'-cyclic nucleotides by fluorescence spectrometry". PLOS ONE. 8 (1) e54158. Bibcode:2013PLoSO...854158R. doi:10.1371/journal.pone.0054158. PMC 3544816. PMID 23342095.
- ^ Rehmann H, Wittinghofer A, Bos JL (January 2007). "Capturing cyclic nucleotides in action: snapshots from crystallographic studies". Nat. Rev. Mol. Cell Biol. 8 (1): 63–73. doi:10.1038/nrm2082. PMID 17183361. S2CID 7216248.
- ^ a b Wolter S, Golombek M, Seifert R (December 2011). "Differential activation of cAMP- and cGMP-dependent protein kinases by cyclic purine and pyrimidine nucleotides". Biochem. Biophys. Res. Commun. 415 (4): 563–6. doi:10.1016/j.bbrc.2011.10.093. PMID 22074826.
- ^ a b Bridges, D; Fraser ME; Moorhead GB (2005). "Cyclic nucleotide binding proteins in the Arabidopsis thaliana and Oryza sativa genomes". BMC Bioinformatics. 6: 6. doi:10.1186/1471-2105-6-6. PMC 545951. PMID 15644130.
- ^ a b Eckly-Michel A, Martin V, Lugnier C (September 1997). "Involvement of cyclic nucleotide-dependent protein kinases in cyclic AMP-mediated vasorelaxation". Br. J. Pharmacol. 122 (1): 158–64. doi:10.1038/sj.bjp.0701339. PMC 1564898. PMID 9298542.
- ^ Holz GG (January 2004). "Epac: A new cAMP-binding protein in support of glucagon-like peptide-1 receptor-mediated signal transduction in the pancreatic beta-cell". Diabetes. 53 (1): 5–13. doi:10.2337/diabetes.53.1.5. PMC 3012130. PMID 14693691.
- ^ Zhou Y, Zhang X, Ebright RH (July 1993). "Identification of the activating region of catabolite gene activator protein (CAP): isolation and characterization of mutants of CAP specifically defective in transcription activation". Proc. Natl. Acad. Sci. U.S.A. 90 (13): 6081–5. Bibcode:1993PNAS...90.6081Z. doi:10.1073/pnas.90.13.6081. PMC 46871. PMID 8392187.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Meiklejohn AL, Gralla JD (December 1985). "Entry of RNA polymerase at the lac promoter". Cell. 43 (3 Pt 2): 769–76. doi:10.1016/0092-8674(85)90250-8. PMID 3907860.
- ^ Desch M, Schinner E, Kees F, Hofmann F, Seifert R, Schlossmann J (September 2010). "Cyclic cytidine 3',5'-monophosphate (cCMP) signals via cGMP kinase I". FEBS Lett. 584 (18): 3979–84. doi:10.1016/j.febslet.2010.07.059. PMID 20691687.
- ^ Beavo, Joseph; Sharron Francis; Miles Houslay (2010). Cyclic Nucleotide Phosphodiesterases in Health and Disease. Boca Raton, FL: CRC Press. p. 546. ISBN 978-0-8493-9668-7.
- ^ Sutherland, Earl; Robison GA; Butcher RW (1968). "Some aspects of the biological role of adenosine 3',5'-monophosphate (cyclic AMP)". Circulation. 37 (2): 279–306. doi:10.1161/01.CIR.37.2.279.
- ^ Lincoln, TM; Cornwell TL (1991). "Towards an understanding of the mechanism of action of cyclic AMP and cyclic GMP in smooth muscle relaxation". Blood Vessels. 28 (1–3): 129–37. doi:10.1159/000158852. PMID 1848122.
External links
[edit]- Nucleotides,+Cyclic at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
Cyclic nucleotide
View on Grokipediafrom Grokipedia
Overview
Definition and Types
Cyclic nucleotides are derivatives of nucleoside monophosphates in which a phosphate group forms a cyclic 3',5'-phosphodiester bond with the ribose sugar moiety, distinguishing them from linear nucleotides.[6] These molecules function primarily as intracellular second messengers in signal transduction pathways, relaying extracellular signals from hormones, neurotransmitters, and other stimuli to elicit diverse cellular responses.[1] Discovered in the late 1950s by Earl W. Sutherland, who identified cyclic AMP as a key mediator of hormonal effects, cyclic nucleotides enable rapid and amplified intracellular communication without direct involvement of the primary signaling molecules.[7] The two primary types of cyclic nucleotides in eukaryotic cells are cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP).[6] These differ structurally in their nitrogenous base: cAMP contains adenine attached to the ribose-phosphate ring, while cGMP features guanine in the same cyclic framework (adenosine 3',5'-cyclic monophosphate versus guanosine 3',5'-cyclic monophosphate).[8] Although other cyclic nucleotides exist in prokaryotes or as bacterial signaling molecules, cAMP and cGMP predominate in mammalian physiology, each modulating distinct yet overlapping cellular functions through interactions with specific effectors.[9] In general, cyclic nucleotides mediate the effects of hormones and neurotransmitters on cellular processes such as metabolism, ion transport, and gene expression by activating downstream targets like protein kinases and ion channels.[10] Their formation occurs via enzymatic cyclization of nucleoside triphosphates, catalyzed by dedicated cyclases: where NTP represents ATP for cAMP or GTP for cGMP, and PPi is pyrophosphate; this reaction is reversible under specific conditions but primarily serves to generate the signaling molecule.[8] This conserved mechanism underscores their role as versatile regulators across cell types and organisms.[6]Discovery and Nomenclature
The discovery of cyclic adenosine monophosphate (cAMP), the first identified cyclic nucleotide, occurred in 1958 through the work of Earl W. Sutherland and his collaborator Theodore W. Rall at Case Western Reserve University. Investigating the mechanism by which hormones like epinephrine and glucagon stimulate glycogenolysis in liver cells, Sutherland's team fractionated liver homogenates and identified a novel compound formed from ATP that mediated the hormonal response. This compound, initially termed a "cyclic adenine ribonucleotide," was produced by particulate fractions of liver tissue upon hormone addition and activated phosphorylase in a subsequent cell-free system.[11][12] Early experimental evidence established cAMP as a heat-stable intracellular factor distinct from the hormones themselves. Using bioassays with liver slices, Sutherland demonstrated that epinephrine rapidly increased phosphorylase activity and glucose release, an effect mimicked by boiled extracts from hormone-treated liver particles but not by the hormones directly. These extracts contained the heat-stable factor, which resisted boiling at 100°C for up to 5 minutes and was later purified and characterized as resistant to phosphatase degradation, confirming its unique cyclic structure. This separation of hormone action into an initial receptor-mediated step and a subsequent intracellular amplification via the stable factor laid the groundwork for understanding signal transduction.[13] The nomenclature "cyclic" derives from the molecule's distinctive 3',5'-phosphodiester bond, linking the 3' and 5' hydroxyl groups of the ribose in adenosine monophosphate, forming a closed ring. In their 1958 publications, Sutherland and Rall described it as adenosine 3',5'-cyclic monophosphate, with the abbreviation cAMP emerging shortly thereafter as the field expanded. By the mid-1960s, as research proliferated, abbreviations like cAMP became standardized in biochemical literature. Similarly, cyclic guanosine monophosphate (cGMP), identified in 1963 from rat urine and mammalian tissues by David F. Ashman and colleagues, followed the same naming convention for its analogous 3',5'-cyclic structure, with cGMP standardized concurrently.[11][12] Initial reception of cAMP as a universal mediator met with skepticism, as many biochemists doubted that a single small molecule could orchestrate diverse hormonal effects across tissues, viewing it instead as a liver-specific intermediate. However, by the mid-1960s, accumulating evidence from multiple systems— including its role in hormone-stimulated lipolysis, steroidogenesis, and ion transport—shifted views, establishing cAMP as a prototypical second messenger. This paradigm shift culminated in Sutherland's sole receipt of the 1971 Nobel Prize in Physiology or Medicine for elucidating hormone action mechanisms through cAMP.[12][14]History
Early Research
The foundations of cyclic nucleotide research trace back to the late 19th and early 20th centuries, when biochemists began elucidating the structure of nucleic acids. Phoebus Levene, working at the Rockefeller Institute, isolated nucleotides as the fundamental units of nucleic acids and identified key components, including the pentose sugar d-ribose from yeast RNA in 1909 and 2-deoxyribose from thymonucleic acid in 1929.[15] These discoveries provided the structural basis for later recognition of cyclic forms, as Levene's analyses revealed phosphate-sugar linkages essential to nucleotide architecture. Concurrently, organic chemists explored cyclic phosphate structures, with syntheses of model cyclic phosphate diesters emerging in the mid-20th century during studies of nucleic acid degradation, highlighting the stability and reactivity of such rings in biological contexts.[16] In the 1940s and 1950s, hormone research increasingly pointed to intracellular mediators in signal transduction, setting the stage for cyclic nucleotide concepts. Earl W. Sutherland initiated studies on epinephrine's activation of liver phosphorylase, observing that hormone effects persisted after cell disruption, suggesting an intermediary substance rather than direct enzyme interaction—a prevailing view at the time. Hans A. Krebs and collaborators advanced metabolic signaling through investigations of cyclic pathways like the citric acid cycle, while researchers such as Lowell and Mary Hokin demonstrated in 1953 that acetylcholine stimulation triggered rapid phosphate incorporation into phosphatidylinositol in pancreas slices, foreshadowing inositol phosphate roles in second messenger systems.[17][18] Pivotal experiments like Otto Loewi's 1921 demonstration of chemical neurotransmission indirectly influenced these developments. By perfusing frog hearts and showing that vagus nerve stimulation released a diffusible inhibitory substance (vagusstoff, later acetylcholine) that slowed a second heart's rate, Loewi established chemical signaling as a biological principle, inspiring inquiries into intracellular chemical relays beyond synapses.[19] A major challenge in pre-1958 research was detecting elusive intracellular mediators at nanomolar concentrations, as available bioassays—such as glycogen breakdown in tissue slices—lacked sensitivity and specificity, often confounded by tissue complexity. Sutherland's 1958 identification of cyclic AMP as the key activator marked the culmination of these foundational efforts.[20][21]Key Milestones
In the 1960s, the identification of cyclic guanosine monophosphate (cGMP) marked a pivotal expansion of cyclic nucleotide research beyond cAMP. First isolated from rat urine in 1963 by Ashman and colleagues (including T. D. Price), cGMP was recognized as a potential second messenger due to its synthesis via guanylate cyclase and degradation by phosphodiesterases, with Ferid Murad and others elucidating its role in rat tissues in the mid-1960s.[22] Concurrently, assays for adenylate cyclase—the enzyme responsible for cAMP production—were refined, enabling precise measurement of cyclic nucleotide levels in cellular extracts and advancing studies on hormone-stimulated signaling.[23] The foundational impact of cyclic nucleotides was formally acknowledged in 1971, when Earl W. Sutherland Jr. received the Nobel Prize in Physiology or Medicine for his discovery of cAMP as an intracellular second messenger mediating hormone actions.[7] This award underscored the paradigm shift toward understanding second messenger systems in signal transduction. During the 1980s and 1990s, research progressed with the development of phosphodiesterase (PDE) inhibitors targeting cGMP degradation, culminating in the synthesis of sildenafil in 1989 as a selective PDE5 inhibitor.[24] Initially explored for cardiovascular applications, sildenafil's potent enhancement of cGMP levels led to its approval in 1998 for erectile dysfunction under the trade name Viagra, demonstrating the therapeutic potential of cyclic nucleotide modulation.[25] Parallel advances included the first crystallographic structures of adenylyl cyclase catalytic domains in complex with G protein subunits, resolved in 1997, which revealed the molecular basis of nucleotide synthesis and regulation. The 1998 Nobel Prize in Physiology or Medicine, awarded to Robert F. Furchgott, Louis J. Ignarro, and Ferid Murad, highlighted the nitric oxide (NO)-cGMP signaling pathway, recognizing NO as an endothelium-derived relaxing factor that activates soluble guanylate cyclase to elevate cGMP levels and mediate vasodilation. From the 2000s onward, cyclic nucleotides were increasingly implicated in non-mammalian organisms, particularly bacteria, where cyclic di-GMP emerged as a key second messenger regulating biofilm formation, motility, and virulence; its role was solidified in the mid-2000s through genomic and biochemical studies across diverse species.[26] Recent technological advances, up to 2025, include cryo-electron microscopy (cryo-EM) structures of cAMP-bound ion channels, such as the human hyperpolarization-activated cyclic nucleotide-gated (HCN) channel HCN3 resolved in 2024, providing atomic insights into ligand-induced gating mechanisms.[27] Similarly, cryo-EM of cAMP-regulated sperm-specific channels in 2023 illuminated conformational dynamics in reproductive signaling.[28]| Year | Milestone | Key Contributors/Publication | Impact |
|---|---|---|---|
| 1963 | Discovery of cGMP in urine | Ashman et al. (including T. D. Price; Biochem Biophys Res Commun) | Established cGMP as a natural cyclic nucleotide beyond cAMP.[23] |
| Mid-1960s | cGMP identified as second messenger in rat tissues | Ferid Murad et al. | Linked cGMP to hormonal and nitroglycerin responses.[22] |
| 1971 | Nobel Prize for cAMP discovery | Earl W. Sutherland Jr. | Validated second messenger concept in hormone signaling.[29] |
| 1987 | Discovery of c-di-GMP in bacteria | Ross et al. (initial report in Komagataeibacter xylinus) | Introduced bacterial cyclic dinucleotides for environmental adaptation.[30] |
| 1989 | Synthesis of sildenafil (PDE5 inhibitor) | Pfizer research team | Pioneered cGMP-targeted therapies for vascular function.[24] |
| 1997 | Crystal structure of adenylyl cyclase | Tesmer et al. (Science) | Revealed G protein-coupled activation mechanism. |
| 1998 | Nobel Prize for NO-cGMP pathway | Furchgott, Ignarro, Murad | Elucidated gasotransmitter role in cardiovascular signaling. |
| Mid-2000s | c-di-GMP as ubiquitous bacterial second messenger | Ute Römling et al. (reviews in Annu Rev Microbiol) | Expanded cyclic nucleotides to microbial physiology and pathogenesis.[26] |
| 2023 | Cryo-EM structure of cAMP-gated sperm channel | Kalienkova et al. (Nature) | Detailed ligand-binding dynamics in fertility.[28] |
| 2024 | Cryo-EM structure of HCN3 with cAMP | Yu et al. (including J. Li; J Biol Chem) | Advanced understanding of cardiac pacemaker regulation.[27] |
Chemical Properties
Molecular Structure
Cyclic nucleotides possess a core molecular structure consisting of a purine nucleobase attached to a ribose sugar via a β-N-glycosidic bond, with a phosphate group forming a cyclic diester linkage between the 3'- and 5'-hydroxyl groups of the ribose. This 3',5'-cyclic phosphodiester bridge creates a strained six-membered ring that is essential for their function as second messengers. In cyclic adenosine monophosphate (cAMP), the nucleobase is adenine, yielding the molecular formula CHNOP; in cyclic guanosine monophosphate (cGMP), it is guanine, resulting in CHNOP. The phosphate group exhibits resonance delocalization across its P-O bonds, which stabilizes the diester configuration and influences the overall planarity of the cyclic moiety.[31][32][33] The stereochemistry of cyclic nucleotides is defined by the β-D-ribofuranose form of the ribose sugar, where the furanose ring adopts a puckered conformation (typically C3'-endo or C2'-endo) and the glycosidic bond orients the base in the anti conformation relative to the ribose. The phosphate linkage maintains a diester geometry with characteristic bond angles around the phosphorus atom, such as O-P-O angles of approximately 100°–110° and P-O-C angles near 120°, as observed in crystallographic studies of analogous cyclic phosphates. These features ensure rigidity and specificity in molecular recognition.[34][35] Positional isomers, such as 2',3'-cyclic nucleotides, occur rarely and arise primarily as intermediates or products of RNA degradation by ribonucleases, lacking the signaling role of the 3',5'-variants due to differences in ring strain and steric accessibility.[36] A key structural distinction between cAMP and cGMP resides in the purine bases: adenine's fixed amino-imino tautomerism in cAMP contrasts with guanine's propensity for keto-enol tautomerism in cGMP, where the enol form at the C6 position can modulate interactions with binding pockets, enhancing specificity for cGMP-dependent targets.[37]Physicochemical Characteristics
Cyclic nucleotides, exemplified by cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), exhibit high water solubility primarily due to the polar, negatively charged phosphate moiety in their ribose-linked structure. This property facilitates their diffusion in aqueous biological environments. For cAMP, solubility is approximately 4 mg/mL in water, and its octanol-water partition coefficient (logP) is -2.96, underscoring its hydrophilic nature.[31][38] These molecules demonstrate relative chemical stability under physiological conditions (pH 7.4, 37°C), where non-enzymatic hydrolysis proceeds slowly, with half-lives extending to several days in buffered solutions. However, they are susceptible to hydrolysis in acidic (pH < 4) or basic (pH > 9) environments, where protonation or deprotonation of the phosphate facilitates ring opening via nucleophilic attack on the phosphorus atom. For instance, in a cobalt(III) complex at pH 8.5 and 50°C, cAMP hydrolysis has a half-life of about 6 days.[39][40] Spectroscopically, cyclic nucleotides display characteristic UV absorption arising from their nucleobase chromophores, with cAMP showing a maximum at 257 nm (ε ≈ 14,000 M⁻¹ cm⁻¹) and cGMP at 252 nm (ε ≈ 13,700 M⁻¹ cm⁻¹). In nuclear magnetic resonance, the ³¹P signal for the cyclic phosphate in cAMP appears around -1 to 0 ppm, reflecting its diester environment, while ¹H NMR shifts for the adenine base protons are typically 8.2 ppm (H-2) and 8.6 ppm (H-8) in neutral aqueous solution.[41][42][43][44] The reactivity of cyclic nucleotides centers on the phosphodiester linkage, which undergoes nucleophilic attack by water or hydroxide ions, leading to cleavage of the 3',5'-cyclic ring and formation of 5'-monophosphate products. This process is enhanced in the presence of metal ions; for example, Mg²⁺ chelates the phosphate oxygens, stabilizing the molecule but also facilitating enzymatic catalysis by lowering the energy barrier for nucleophilic approach.[45][46] To overcome limitations in cellular uptake due to their polarity, analogs such as N⁶,O²'-dibutyryl-cAMP (dbcAMP) incorporate acyl groups on the exocyclic amino and ribose hydroxyls, boosting lipophilicity (logP > -1) and membrane permeability while retaining bioactivity after intracellular deacylation. These modifications also confer resistance to non-specific hydrolysis.[47][48]Biosynthesis and Metabolism
Enzymatic Synthesis
Cyclic nucleotides, such as cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), are synthesized enzymatically from nucleotide triphosphates within cellular compartments.[49] The primary enzyme for cAMP production is adenylyl cyclase (AC), which catalyzes the conversion of adenosine triphosphate (ATP) to cAMP and pyrophosphate (PPi).87445-8/fulltext) In mammals, there are ten isoforms of AC, including nine membrane-bound isoforms (AC1–AC9) that are integral to the plasma membrane and one soluble isoform (sAC or AC10) located in the cytosol.[50] The membrane-bound isoforms are primarily regulated by heterotrimeric G proteins; activation occurs through stimulatory G proteins (Gs) that enhance AC activity, while inhibitory G proteins (Gi) suppress it, allowing precise control in response to G protein-coupled receptor signaling. The reaction proceeds as follows: This cyclization involves an inline attack by the 3'-hydroxyl group of the ribose on the α-phosphate of ATP, displacing PPi without net hydrolysis of water.[51] For cGMP synthesis, guanylate cyclase (GC) converts guanosine triphosphate (GTP) to cGMP and PPi.[52] Mammals express two main forms of GC: soluble guanylate cyclase (sGC), a cytosolic heterodimer activated by nitric oxide (NO), and particulate guanylate cyclase (pGC), a family of seven transmembrane receptors (GC-A through GC-G) activated by peptide ligands such as atrial natriuretic peptide.[53] In sGC, regulation involves NO binding to a heme prosthetic group, which induces a conformational change for allosteric activation and enhanced catalytic activity.00107-1/fulltext) The core reaction is: pGC isoforms are embedded in the plasma membrane, while sGC operates in the cytosol, enabling localized signaling.[54] Synthesis of both cAMP and cGMP occurs within specialized cellular microdomains, such as lipid rafts or protein complexes, which restrict diffusion and ensure spatially confined second messenger production for targeted physiological responses.[49]Degradation Pathways
The degradation of cyclic nucleotides, such as cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), is primarily mediated by a superfamily of enzymes known as phosphodiesterases (PDEs), which hydrolyze these second messengers to their respective linear 5'-monophosphates, 5'-AMP and 5'-GMP, thereby terminating their signaling roles. There are 11 distinct PDE families (PDE1 through PDE11), each with specific substrate preferences: some are cAMP-specific (e.g., PDE4, PDE7, PDE8), others are cGMP-specific (e.g., PDE5, PDE6, PDE9), and several exhibit dual specificity (e.g., PDE1, PDE2, PDE3, PDE10, PDE11). For instance, PDE4 selectively hydrolyzes cAMP, playing a key role in immune and inflammatory responses.[55][56][57] The catalytic mechanism of PDEs involves the hydrolysis of the 3'-phosphodiester bond in the cyclic nucleotide ring, facilitated by a conserved catalytic domain that coordinates two metal ions, typically Mg²⁺ and a second divalent cation like Zn²⁺ or Fe²⁺, to activate water for nucleophilic attack. This process can be represented by the general reaction: PDE activity results in rapid turnover of cyclic nucleotides, with half-lives typically ranging from seconds to minutes in cellular contexts, depending on isoform expression, substrate concentration, and compartmentalization.[55][57][2] PDEs are subject to multifaceted regulation to fine-tune cyclic nucleotide levels, including isoform-specific subcellular localization—such as cytosolic for PDE4, membrane-associated for PDE3 in cardiac myocytes, or photoreceptor-specific for PDE6—and pharmacological inhibition. For example, rolipram selectively inhibits PDE4, elevating cAMP in targeted compartments like immune cells and airway smooth muscle. Additionally, PDEs can be modulated by phosphorylation, allosteric effectors (e.g., cGMP binding to PDE2 or PDE3), and anchoring to scaffolds like AKAPs, ensuring spatially restricted degradation.[55][58][59]Molecular Mechanisms
Target Interactions
Cyclic nucleotides, such as cyclic AMP (cAMP) and cyclic guanosine monophosphate (cGMP), exert their effects by binding to specific protein targets, primarily through conserved cyclic nucleotide-binding domains (CNBDs). These domains feature a β-barrel structure with a hydrophobic pocket that accommodates the purine base and ribose of the cyclic nucleotide, while a C-terminal α-helix acts as a hinged lid to stabilize the bound ligand.[60] The binding affinity varies by target, enabling precise modulation of downstream activities at physiological concentrations. One primary target is protein kinase A (PKA), a serine/threonine kinase activated by cAMP. In its inactive holoenzyme form (R₂C₂, where R denotes regulatory subunits and C catalytic subunits), cAMP binds to the two identical regulatory subunits, each containing two CNBDs, causing a conformational change that dissociates the catalytic subunits for substrate phosphorylation. The dissociation constant (K_d) for cAMP binding to PKA regulatory subunits is approximately 100 nM, reflecting high affinity.[61] This activation can be represented by the equation: Another important cAMP target is the exchange protein directly activated by cAMP (EPAC), a guanine nucleotide exchange factor for small GTPases Rap1 and Rap2. EPAC contains a single CNBD and is activated by cAMP binding, which induces a conformational change to promote GDP/GTP exchange on Rap proteins, independent of PKA. EPACs mediate diverse processes including cell adhesion, secretion, and neuronal plasticity.[62] Protein kinase G (PKG), activated by cGMP, shares structural similarities with PKA but exists in two main isoforms: PKG-I (with splice variants α and β) and PKG-II. cGMP binding to the regulatory domains of these isoforms relieves autoinhibition, allowing the catalytic domains to phosphorylate targets; PKG-I is soluble and dimerizes via an N-terminal leucine zipper, while PKG-II is membrane-associated.[63][64] Cyclic nucleotides also directly modulate ion channels. In olfaction, cyclic nucleotide-gated (CNG) channels in sensory neurons are activated by cAMP binding to their CNBDs, permitting cation influx to depolarize the cell. Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, found in pacemaker cells, are shifted toward more positive voltages by cAMP binding, enhancing channel opening.[65][66] Intracellular levels of cyclic nucleotides, regulated by synthesis and degradation, determine the extent of these interactions.[61]Signaling Cascades
Cyclic nucleotides, such as cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), serve as second messengers that propagate extracellular signals through intricate signaling cascades, enabling rapid and amplified cellular responses. These cascades typically involve the activation of kinases that phosphorylate downstream targets, leading to diverse physiological outcomes like gene expression and cytoskeletal changes. The integration of multiple enzymatic steps allows for signal amplification and fine-tuned regulation, ensuring specificity in cellular communication. A prominent example is the cAMP-PKA-CREB pathway, initiated by hormones binding to G-protein-coupled receptors, which activate adenylyl cyclase (AC) to produce cAMP from ATP. Elevated cAMP binds to the regulatory subunits of protein kinase A (PKA), releasing its catalytic subunits to phosphorylate various substrates. In the nucleus, PKA phosphorylates the transcription factor CREB at serine 133, promoting its binding to cAMP response elements (CRE) in DNA and facilitating transcription of target genes involved in cell survival and differentiation. This pathway was foundational in establishing second messenger concepts, with cAMP's role in hormonal signaling first elucidated in the late 1950s.[1] Similarly, the cGMP-PKG-NO pathway is triggered by nitric oxide (NO), often produced by nitric oxide synthase in response to stimuli like shear stress or neurotransmitters. NO activates soluble guanylate cyclase (sGC), which converts GTP to cGMP, activating protein kinase G (PKG). PKG phosphorylates targets such as myosin light chain phosphatase, leading to dephosphorylation of myosin light chain and smooth muscle relaxation, a mechanism critical for vasodilation. This cascade's discovery in the 1980s revolutionized understanding of endothelial-derived relaxing factors, with NO identified as the key signaling molecule. Crosstalk between cAMP and cGMP pathways occurs primarily through phosphodiesterases (PDEs), enzymes that hydrolyze both cyclic nucleotides, thereby modulating their local concentrations and preventing indiscriminate signaling. For instance, PDE2, which is activated by cGMP, degrades cAMP, while PDE3 inhibition by cGMP elevates cAMP levels, influencing cardiac contractility and vascular tone. Additionally, feedback loops involving phosphatases, such as protein phosphatase 1 (PP1) and PP2A, counteract kinase activities; PKA can phosphorylate and regulate these phosphatases, or intermediaries like DARPP-32 inhibit PP1 to sustain phosphorylation states, creating negative feedback to terminate signals. These interactions ensure balanced cross-regulation, as demonstrated in cardiac and neuronal contexts.[67] Signal amplification is a hallmark of these cascades, where a single activated AC or sGC molecule can generate thousands of cyclic nucleotide molecules per second, exponentially increasing second messenger levels from one receptor activation event. This enzymatic turnover rate, combined with downstream kinase activation where one PKA holoenzyme phosphorylates multiple substrates, amplifies the initial signal by orders of magnitude, enabling sensitive detection of low-level stimuli. Compartmentalization further refines these cascades through A-kinase anchoring proteins (AKAPs), which scaffold PKA, AC, PDEs, and phosphatases into discrete microdomains near specific targets, such as ion channels or transcription factors. By localizing signaling components, AKAPs prevent diffusion-mediated crosstalk and allow spatially restricted responses, as seen in cardiomyocytes where AKAPs organize PKA near ryanodine receptors for precise calcium handling. This scaffolding mechanism enhances efficiency and specificity in cyclic nucleotide signaling.Biological Roles
Cellular Functions
Cyclic nucleotides play pivotal roles in regulating intracellular processes essential for cellular homeostasis and adaptation. In glycogen metabolism, cyclic AMP (cAMP) activates protein kinase A (PKA), which in turn phosphorylates and activates phosphorylase kinase in liver and muscle cells, thereby promoting glycogenolysis to mobilize glucose during energy demands such as fasting or exercise.[69] This activation cascade ensures rapid glucose release, with PKA-mediated phosphorylation increasing phosphorylase kinase activity by up to several-fold, highlighting cAMP's role in metabolic switching.[70] Cyclic AMP also modulates gene expression by influencing transcription factors that bind to cAMP response elements (CREs) in promoter regions. Specifically, cAMP elevates levels of phosphorylated CREB (cAMP response element-binding protein) and related ATF (activating transcription factor) family members, such as ATF-1, which form homodimers or heterodimers to enhance transcription of target genes involved in cellular adaptation and survival.[71] These factors bind the consensus CRE sequence (TGACGTCA), driving expression of genes like those encoding enzymes for gluconeogenesis or stress-responsive proteins, with CREB phosphorylation at serine 133 being a key regulatory step.[72] In maintaining ion homeostasis, cyclic GMP (cGMP) regulates the cystic fibrosis transmembrane conductance regulator (CFTR), a chloride channel critical for epithelial fluid secretion. cGMP activates protein kinase G (PKG), which phosphorylates CFTR to open the channel, facilitating chloride efflux and subsequent water movement across epithelia in tissues like the intestine and airways.[73] This mechanism is particularly evident in secretory responses, where elevated cGMP, often from nitric oxide signaling, enhances CFTR conductance to prevent ion imbalances.[74] Cyclic AMP exerts antiproliferative effects in certain cancer cells through the exchange protein directly activated by cAMP (EPAC) pathway, which engages Rap1 to suppress growth signaling. In prostate carcinoma cells, for instance, EPAC activation by cAMP inhibits mitogen-activated protein kinase (MAPK) and RhoA pathways, reducing cell proliferation and migration by altering cytoskeletal dynamics and gene expression profiles.[75] This Rap1-mediated suppression underscores cAMP's tumor-suppressive potential via non-PKA effectors.[76] Furthermore, nitric oxide influences autophagy and cellular stress responses by modulating the mechanistic target of rapamycin (mTOR) pathway. Nitric oxide activates PKG-independent mechanisms to inhibit autophagy induction under stress by sustaining mTORC1 activity, thereby promoting protein synthesis and cell survival during nutrient or oxidative challenges.[77] This regulatory axis helps maintain proteostasis.Physiological Effects
In the cardiovascular system, cyclic GMP (cGMP) signaling through protein kinase G (PKG) mediates vasodilation by promoting smooth muscle relaxation in blood vessels.[78] Nitric oxide stimulates soluble guanylate cyclase to elevate cGMP levels, which activates PKG to phosphorylate targets such as myosin light chain phosphatase, reducing vascular tone and facilitating blood flow.[79] Additionally, cGMP-PKG pathway inhibits platelet aggregation by suppressing activation and promoting disaggregation, thereby preventing thrombus formation.[80] In the nervous system, cyclic AMP (cAMP) contributes to synaptic plasticity and learning processes, notably through its role in long-term potentiation (LTP) at hippocampal synapses.[81] Elevation of cAMP activates protein kinase A (PKA), which enhances AMPA receptor trafficking and stabilizes synaptic strengthening in the hippocampus, supporting memory consolidation.[82] In the endocrine system, cAMP regulates hormone secretion, exemplified by its amplification of insulin release from pancreatic beta cells in response to glucose.[83] Glucose-induced cAMP production potentiates exocytosis via PKA-dependent phosphorylation of ion channels and Epac-mediated activation of Ras-related proteins, ensuring pulsatile insulin output.[84] In sensory systems, cGMP drives phototransduction in retinal rods and cones by gating cyclic nucleotide-gated channels that maintain the dark current.[85] Light-activated rhodopsin triggers phosphodiesterase to hydrolyze cGMP, closing these channels and hyperpolarizing photoreceptors to initiate visual signaling.[86] In olfaction, cGMP modulates odorant sensitivity in vertebrate sensory neurons by interacting with cyclic nucleotide-gated channels, fine-tuning transduction alongside cAMP pathways.[87] In non-mammalian organisms, cyclic di-GMP (c-di-GMP) in bacteria orchestrates biofilm formation by upregulating adhesins and extracellular matrix production, enabling surface attachment and community development.[88] Elevated c-di-GMP levels shift bacteria from motile planktonic states to sessile biofilms, enhancing survival in hostile environments.[89] In plants, cyclic nucleotides such as cAMP and cGMP mediate stress responses, activating defense signaling against biotic pathogens and abiotic factors like drought or salinity.[90] These messengers regulate ion channel activity and gene expression to bolster tolerance and adaptive growth under stress.[91]Clinical and Research Implications
Associated Diseases
Disruptions in cyclic nucleotide signaling pathways are implicated in various diseases, particularly those involving impaired ion transport, vascular function, cellular proliferation, and neurodegeneration. In cystic fibrosis, mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene lead to defective chloride channel function, as CFTR is a cAMP- and cGMP-regulated chloride and bicarbonate channel essential for epithelial ion transport.[92] These mutations, such as the common ΔF508 deletion, reduce cAMP-dependent phosphorylation and ATP gating of CFTR, resulting in diminished chloride secretion and thickened mucus in airways and other epithelia, exacerbating chronic infections and inflammation.[93] The CFTR defect thereby impairs overall fluid homeostasis, contributing to the multisystem pathology of the disease.[94] In heart failure, alterations in cGMP signaling play a key role, especially in conditions like pulmonary hypertension where reduced cGMP levels impair vasodilation and promote vascular remodeling.[95] Overexpression of phosphodiesterase 5 (PDE5), which hydrolyzes cGMP, is observed in failing human hearts and contributes to decreased cGMP bioavailability, exacerbating contractile dysfunction and hypertrophy.[96] This PDE5 upregulation is particularly pronounced in advanced cardiomyopathy, linking cyclic nucleotide degradation to progressive cardiac remodeling and systolic impairment.[97] Cyclic nucleotide dysregulation also drives certain cancers through aberrant adenylyl cyclase (AC) activation. In pituitary tumors, particularly growth hormone-secreting adenomas, GTPase-inhibiting mutations in the GNAS gene (gsp oncogene) constitutively activate the stimulatory G protein α-subunit (Gsα), leading to persistent AC stimulation and elevated cAMP levels that promote tumor growth and hormone hypersecretion.[98] These mutations occur in approximately 35-40% of acromegaly-associated somatotroph adenomas, correlating with higher cAMP-dependent protein kinase A activity and aggressive tumor behavior.[99] Similarly, in thyroid adenomas, Gsα mutations cause autonomous cAMP elevation, fostering hyperfunctioning nodules that produce excess thyroid hormones independently of TSH stimulation.[100] Such mutations are found in approximately 5-10% of toxic thyroid adenomas, enhancing proliferation via cAMP-mediated pathways.[101] Neurodegenerative disorders like Alzheimer's disease involve cGMP dysregulation through the nitric oxide-soluble guanylyl cyclase (NO-sGC) pathway, where impaired NO production or sGC activity reduces cGMP levels, contributing to synaptic dysfunction and amyloid-β accumulation.[102] In Alzheimer's models, diminished NO-sGC-cGMP signaling disrupts neuronal plasticity and exacerbates tau hyperphosphorylation, with postmortem brain analyses showing lowered cGMP in affected regions.[103] This pathway's downregulation correlates with cognitive decline, as restoring cGMP via sGC stimulation ameliorates memory deficits in preclinical studies.[104] Recent insights from 2025 highlight the role of bacterial cyclic di-GMP (c-di-GMP) signaling in antibiotic-resistant infections, where analogs targeting c-di-GMP pathways show promise in disrupting biofilm formation and virulence without inducing resistance.[105] In pathogens like Pseudomonas aeruginosa and Staphylococcus species, elevated intracellular c-di-GMP promotes persistence in chronic infections by enhancing adhesion and stress tolerance, and novel c-di-GMP analogs inhibit diguanylate cyclases to sensitize biofilms to conventional antibiotics.[106] These developments underscore c-di-GMP's potential as a target for combating multidrug-resistant infections in clinical settings.[107]Therapeutic Applications
Cyclic nucleotide pathways have been targeted therapeutically through phosphodiesterase (PDE) inhibitors, which prevent the degradation of cAMP and cGMP to elevate their intracellular levels. Sildenafil, a selective PDE5 inhibitor, increases cGMP in vascular smooth muscle, leading to vasodilation and its primary use in treating erectile dysfunction by enhancing penile blood flow.[108] Roflumilast, a PDE4 inhibitor, elevates cAMP in inflammatory cells, reducing cytokine production and bronchoconstriction, and is approved for maintenance treatment of severe chronic obstructive pulmonary disease (COPD) in patients with chronic bronchitis.[109] Adenylyl cyclase (AC) activators stimulate cAMP production and have applications in cardiovascular and research settings. Forskolin, a diterpene derived from Coleus forskohlii, directly activates AC isoforms, promoting smooth muscle relaxation, and is used clinically in topical formulations to lower intraocular pressure in glaucoma while also showing potential in cardiovascular conditions through its inotropic effects.[110] NKH477, a water-soluble forskolin analog, potently activates cardiac AC type V, increasing contractility and heart rate, and has been evaluated in clinical trials for acute heart failure management due to its positive inotropic and vasodilatory properties.[111] Cyclic nucleotide analogs serve as cell-permeable mimics for research and potential therapeutic modulation of signaling pathways. Dibutyryl-cAMP (db-cAMP), a lipophilic derivative of cAMP, diffuses across cell membranes to activate protein kinase A, commonly used in laboratory studies of cAMP-dependent processes and showing anticancer effects by inhibiting tumor growth in preclinical models.[112] Sp-8-Br-cAMPS, a bromine-substituted cAMP analog, acts as a selective agonist for cAMP-dependent protein kinase type I, enabling precise dissection of signaling cascades in cellular research with minimal off-target effects compared to other analogs. Diagnostic tools targeting cyclic nucleotides include enzyme-linked immunosorbent assay (ELISA) kits that quantify cAMP and cGMP levels in biological fluids. These assays detect sub-picomolar concentrations in plasma, serum, urine, and saliva, aiding in the evaluation of endocrine disorders such as hyperparathyroidism or adrenal dysfunction where altered cyclic nucleotide excretion reflects hormonal imbalances.[113] Emerging therapies leverage genetic and immunological approaches to modulate cyclic nucleotide signaling. Gene therapies aimed at enhancing adenylyl cyclase activity via overexpression of functional isoforms are under investigation for cardiovascular diseases, with viral vectors delivering functional AC isoforms to restore cAMP signaling in failing hearts.[114] Additionally, cyclic di-GMP (c-di-GMP), a bacterial second messenger, is being explored in vaccine formulations to enhance immune responses against pathogens by activating host STING pathways and promoting adjuvanticity in antibacterial vaccines.[115]References
- https://www.sciencedirect.com/topics/[neuroscience](/page/Neuroscience)/cyclic-adenosine-monophosphate