Chemistry:Cyclic guanosine monophosphate

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Cyclic guanosine monophosphate
Skeletal formula of cyclic guanosine monophosphate
Space-filling model of the cyclic guanosine monophosphate anion
Names
IUPAC name
Guanosine 3′,5′-(hydrogen phosphate)
Systematic IUPAC name
2-Amino-9-[(4aR,6R,7R,7aS)-2,7-dihydroxy-2-oxotetrahydro-2H,4H-2λ5-furo[3,2-d][1,3,2]dioxaphosphol-6-yl]-3,9-dihydro-6H-purin-6-one
Other names
cGMP; 3′,5′-Cyclic GMP; Guanosine cyclic monophosphate; Cyclic 3′,5′-GMP; Guanosine 3′,5′-cyclic phosphate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
MeSH Cyclic+GMP
UNII
Properties
C10H12N5O7P
Molar mass 345.208 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
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Cyclic guanosine monophosphate (cGMP) is a cyclic nucleotide derived from guanosine triphosphate (GTP). cGMP acts as a second messenger much like cyclic AMP. Its most likely mechanism of action is activation of intracellular protein kinases in response to the binding of membrane-impermeable peptide hormones to the external cell surface.[1] Through protein kinases activation, cGMP can relax smooth muscle.[2] cGMP concentration in urine can be measured for kidney function and diabetes detection.[3]

Synthesis

Guanylate cyclase (GC) catalyzes cGMP synthesis. This enzyme converts GTP to cGMP. Peptide hormones such as the atrial natriuretic factor activate membrane-bound GC, while soluble GC (sGC) is typically activated by nitric oxide to stimulate cGMP synthesis. sGC can be inhibited by ODQ (1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one).[4]

Functions

cGMP is a common regulator of ion channel conductance, glycogenolysis, and cellular apoptosis. It also relaxes smooth muscle tissues. In blood vessels, relaxation of vascular smooth muscles leads to vasodilation and increased blood flow. At presynaptic terminals in the striatum, cGMP controls the efficacy of neurotransmitter release.[5]

cGMP is a secondary messenger in phototransduction in the eye. In the photoreceptors of the mammalian eye, the presence of light activates phosphodiesterase, which degrades cGMP. The sodium ion channels in photoreceptors are cGMP-gated, so degradation of cGMP causes sodium channels to close, which leads to the hyperpolarization of the photoreceptor's plasma membrane and ultimately to visual information being sent to the brain.[6]

cGMP is also seen to mediate the switching on of the attraction of apical dendrites of pyramidal cells in cortical layer V towards semaphorin-3A (Sema3a).[7] Whereas the axons of pyramidal cells are repelled by Sema3a, the apical dendrites are attracted to it. The attraction is mediated by the increased levels of soluble guanylate cyclase (SGC) that are present in the apical dendrites. SGC generates cGMP, leading to a sequence of chemical activations that result in the attraction towards Sema3a. The absence of SGC in the axon causes the repulsion from Sema3a. This strategy ensures the structural polarization of pyramidal neurons and takes place in embryonic development.

cGMP, like cAMP, gets synthesized when olfactory receptors receive odorous input. cGMP is produced slowly and has a more sustained life than cAMP, which has implicated it in long-term cellular responses to odor stimulation, such as long-term potentiation. cGMP in the olfactory is synthesized by both membrane guanylyl cyclase (mGC) as well as soluble guanylyl cyclase (sGC). Studies have found that cGMP synthesis in the olfactory is due to sGC activation by nitric oxide, a neurotransmitter. cGMP also requires increased intracellular levels of cAMP and the link between the two second messengers appears to be due to rising intracellular calcium levels.[8]

Degradation

Numerous cyclic nucleotide phosphodiesterases (PDE) can degrade cGMP by hydrolyzing cGMP into 5'-GMP. PDE 5, -6 and -9 are cGMP-specific while PDE1, -2, -3, -10 and -11 can hydrolyse both cAMP and cGMP.

Phosphodiesterase inhibitors prevent the degradation of cGMP, thereby enhancing and/or prolonging its effects. For example, Sildenafil (Viagra) and similar drugs enhance the vasodilatory effects of cGMP within the corpus cavernosum by inhibiting PDE 5 (or PDE V). This is used as a treatment for erectile dysfunction. However, the drug can inhibit PDE6 in retina (albeit with less affinity than PDE5). This has been shown to result in loss of visual sensitivity but is unlikely to impair common visual tasks, except under conditions of reduced visibility when objects are already near visual threshold.[9] This effect is largely avoided by other PDE5 inhibitors, such as tadalafil.[10]

role of PKG in cellular system

Protein kinase activation

cGMP is involved in the regulation of some protein-dependent kinases. For example, PKG (protein kinase G) is a dimer consisting of one catalytic and one regulatory unit, with the regulatory units blocking the active sites of the catalytic units.

cGMP binds to sites on the regulatory units of PKG and activates the catalytic units, enabling them to phosphorylate their substrates. Unlike with the activation of some other protein kinases, notably PKA, the PKG is activated but the catalytic and regulatory units do not disassociate.

See also

References

  1. ↑ "Cyclic nucleotide-dependent protein kinases: intracellular receptors for cAMP and cGMP action". Critical Reviews in Clinical Laboratory Sciences 36 (4): 275–328. August 1999. doi:10.1080/10408369991239213. PMID 10486703. 
  2. ↑ "Molecular mechanism of cGMP-mediated smooth muscle relaxation". Journal of Cellular Physiology 184 (3): 409–420. September 2000. doi:10.1002/1097-4652(200009)184:3<409::aid-jcp16>3.0.co;2-k. PMID 10911373. 
  3. ↑ Shimosawa, Tatsuo, ed (2018-04-12). "Urinary cGMP predicts major adverse renal events in patients with mild renal impairment and/or diabetes mellitus before exposure to contrast medium". PLOS ONE 13 (4): e0195828. doi:10.1371/journal.pone.0195828. PMID 29649334. Bibcode: 2018PLoSO..1395828C. 
  4. ↑ "Potent and selective inhibition of nitric oxide-sensitive guanylyl cyclase by 1H-[1,2,4oxadiazolo[4,3-a]quinoxalin-1-one"]. Molecular Pharmacology 48 (2): 184–188. August 1995. PMID 7544433. https://molpharm.aspetjournals.org/content/48/2/184. 
  5. ↑ "Presynaptic cGMP sets synaptic strength in the striatum and is important for motor learning". EMBO Reports 23 (8): e54361. August 2022. doi:10.15252/embr.202154361. PMID 35735260. 
  6. ↑ "The pharmacology of cyclic nucleotide-gated channels: emerging from the darkness". Current Pharmaceutical Design 12 (28): 3597–3613. 2006. doi:10.2174/138161206778522100. NIHMSID: NIHMS47625. PMID 17073662. 
  7. ↑ "Semaphorin 3A is a chemoattractant for cortical apical dendrites". Nature 404 (6778): 567–573. April 2000. doi:10.1038/35007001. PMID 10766232. Bibcode: 2000Natur.404..567P. 
  8. ↑ "Interplay among cGMP, cAMP, and Ca2+ in living olfactory sensory neurons in vitro and in vivo". The Journal of Neuroscience 31 (23): 8395–8405. June 2011. doi:10.1523/JNEUROSCI.6722-10.2011. PMID 21653844. 
  9. ↑ "The effect of sildenafil citrate (Viagra) on visual sensitivity". Journal of Vision 7 (8): 4. June 2007. doi:10.1167/7.8.4. PMID 17685811. 
  10. ↑ "The discovery of tadalafil: a novel and highly selective PDE5 inhibitor. 2: 2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione analogues". Journal of Medicinal Chemistry 46 (21): 4533–4542. October 2003. doi:10.1021/jm0300577. PMID 14521415. 



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