» Articles » PMID: 7582473

Additive Effect of ADP and CGRP in Modulation of the Acetylcholine Receptor Channel in Xenopus Embryonic Myocytes

Overview
Journal Br J Pharmacol
Publisher Wiley
Specialty Pharmacology
Date 1995 Jun 1
PMID 7582473
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

1. We have previously shown that the activation of either protein kinase A (PKA) or protein kinase C (PKC) enhanced the responses of muscle membrane to acetylcholine (ACh) by increasing the mean open time of embryonic-type ACh channels in Xenopus cultured myocytes. In the present study, we further investigated the interaction between these two kinases in the modulation of ACh channels by using the receptor ligands, adenosine diphosphate (ADP) and calcitonin gene-related peptide (CGRP) which selectively activate PKC and PKA, respectively. 2. ADP concentration-dependently increased the mean open time of embryonic-type ACh channels and 0.3 mM ADP is sufficient to achieve the maximal potentiating effect. alpha, beta-Methylene ATP and PMA (phorbol 12-myristate 13-acetate) but not adenosine, AMP, dibutyryl cyclic GMP have similar potentiating action. 3. Suramin (0.3 mM) pretreatment abolished the potentiating effect of ADP but left that of PMA unchanged. 4. CGRP increased the mean open time of embryonic-type ACh channels in a concentration-dependent manner and 1 microM CGRP produced the maximal effect. 5. The maximal effects of both ADP (0.3 mM) and CGRP (1 microM) in the prolongation of mean open time of ACh channels were additive. 6. These results suggest that the modulation of embryonic-type ACh channels by the endogenously released ligands via the activation of PKA and PKC is additive and possibly different sites of ACh channels may be involved in the potentiation effect of either PKC or PKA.

Citing Articles

P2 Receptor Signaling in Motor Units in Muscular Dystrophy.

Khairullin A, Grishin S, Ziganshin A Int J Mol Sci. 2023; 24(2).

PMID: 36675094 PMC: 9865441. DOI: 10.3390/ijms24021587.


Regulation of Carcinogenesis by Sensory Neurons and Neuromediators.

Erin N, Shurin G, Baraldi J, Shurin M Cancers (Basel). 2022; 14(9).

PMID: 35565462 PMC: 9102554. DOI: 10.3390/cancers14092333.


Calcitonin gene-related peptide (CGRP): A novel target for Alzheimer's disease.

Singh Y, Gupta G, Shrivastava B, Dahiya R, Tiwari J, Ashwathanarayana M CNS Neurosci Ther. 2017; 23(6):457-461.

PMID: 28417590 PMC: 6492742. DOI: 10.1111/cns.12696.

References
1.
Dowdall M, Boyne A, Whittaker V . Adenosine triphosphate. A constituent of cholinergic synaptic vesicles. Biochem J. 1974; 140(1):1-12. PMC: 1167964. DOI: 10.1042/bj1400001. View

2.
Albuquerque E, Deshpande S, Aracava Y, Alkondon M, Daly J . A possible involvement of cyclic AMP in the expression of desensitization of the nicotinic acetylcholine receptor. A study with forskolin and its analogs. FEBS Lett. 1986; 199(1):113-20. DOI: 10.1016/0014-5793(86)81235-2. View

3.
Teichberg V, Sobel A, Changeux J . In vitro phosphorylation of the acetylcholine receptor. Nature. 1977; 267(5611):540-2. DOI: 10.1038/267540a0. View

4.
Greengard P . Phosphorylated proteins as physiological effectors. Science. 1978; 199(4325):146-52. DOI: 10.1126/science.22932. View

5.
Zimmermann H . Turnover of adenine nucleotides in cholinergic synaptic vesicles of the Torpedo electric organ. Neuroscience. 1978; 3(9):827-36. DOI: 10.1016/0306-4522(78)90035-0. View