Summary
Basal adenosine 3′,5′-cyclic monophosphate (cAMP) content and the modulation of its production were studied in the frog's semicircular canal epithelium. This epithelium secretes endolymph, a K+-rich, positively polarized fluid. The basal cAMP content measured by microradioimmunoassay was 244 ± 14.2 fmol/structure per 5 min (n = 30). This content was increased about 8 times by 10−5 M forskolin. Vasotocin, the frog antidiuretic hormone, increased the cAMP production by factors of 1.3 and 3.3 at concentrations of 10−8 M and 10−7 M, respectively. This stimulatory effect of vasotocin was blunted by the addition of α2-adrenergic agonists, such as 10−8 M-10−5 M norepinephrine, in the presence of 10−5 M propranolol, or 10−5 M clonidine. Prostaglandin E2 at a concentration of 10−8 M, which did not affect the cAMP production, did not modify the response to vasotocin. Glucagon (10−6 M), calcitonin (10−6 M), and parathyroid hormone (10 units/ml) did not affect the cAMP content. Prostaglandin E2 (10−7 M) and the β-adrenergic agonist isoproterenol (10−6 M) stimulated the cAMP production by a factor of 1.6. These results indicate that the frog semicircular canal is a target of both vasotocin and catecholamines and that catecholamines through α2-receptors modulate vasotocin-induced cAMP generation. Further, this interaction might be of physiological relevance in the modulation of ion transport in this structure.
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References
Ahlström P, Thalmann I, Thalmann R, Ise I (1975) Cyclic AMP and adenylate cyclase in the inner ear. Laryngoscope 85: 1241–1258
Anniko M, Spangberg ML, Schacht J (1981) Adenylate cyclase activity in the fetal and early postnatal inner ear of the mouse. Hear Res 4:11–22
Bagger-Sjöbäck D, Filipek CS, Schacht J (1980) Characteristics and drug responses of cochlear and vestibular adenylate cyclase. Arch Otorhinolaryngol 228:217–222
Bentley PJ (1969) Neurohypophysial function in amphibia: hormone activity in the plasma. J Endocrinol 43:359–369
Bernard C, Ferrary E, Sterkers O (1986) Production of endolymph in the semicircular canal of the frog Rana esculenta. J Physiol (Lond) 371:17–28
Brooker G, Harper JF, Terasaki WL, Moylan RD (1979) Radioimmunoassay of cyclic AMP and cyclic GMP. Adv Cyclic Nucleotide Res 10: 2–3
Chabardes D, Montegut M, Imbert-Teboul M, Morel F (1984) Inhibition of α2-adrenergic agonists of AVP-induced cAMP accumulation in isolated collecting tubule of the rat kidney. Mol Cell Endocrinol 37:263–275
Escoubet B, Amsallem P, Ferrary E, Tran Ba Huy P (1985) Prostaglandin synthesis by the cochlea of the guinea pig. Influence of aspirin, gentamicin and acoustic stimulation. Prostaglandins 29:589–600
Feldman AM, Brusilow SW (1976) Effects of cholera toxin on cochlear endolymph production: model for endolymphatic hydrops. Proc Natl Acad Sci USA 73:1761–1764
Ferrary E, Bernard C, Sterkers O, Escoubet B (1987) Prostaglandins in the semicircular canal of the frog.0 Hear Res 26:139–144
Ferrary E, Bernard C, Sterkers O, Amiel C (1989) Sodium transfer from endolymph through a luminal amiloride-sensitive channel. Am J Physiol 257: F182-F189
Friedlander G, Amiel C (1986) Somatostatin and α2-adrenergic agonists selectively inhibit vasopressin-induced cyclic AMP accumulation in MDCK cells. FEBS Lett 198:38–42
Herman CA, Shinholser RL, Lujan MD (1985) Comparative effects of prostaglandin E2 and prostaglandin E3 on water flow and cyclic AMP in the urinary bladder of the frog Rana pipiens. Prostaglandins 29:629–642
Koch T, Zenner HP (1988) Adenylate cyclase and G-proteins as a signal transfer system in the guinea pig inner ear. Arch Otorhinolaryngol 245:82–87
Mees K (1984) Cytochemical localization of adenyleyclase in the lateral wall of the inner ear. Arch Otorhinolaryngol 240: 55–61
Mishina T, Shimada H, Marumo F (1983) Stimulatory and inhibitory effects of guanine nucleotides on arginin-vasotocinsensitive adenylate cyclase in the epithelial cell membranes of the bullfrog bladder. J Endocrinol 99:269–279
Oudar O, Ferrary E, Feldmann G (1990) Adenylate cyclase and carbonic anhydrase in the frog Rana esculenta semicircular canal epithelium: an ultrastructural cytochemical localization. Cell Tissue Res 262:579–585
Paloheimo S, Thalmann R (1977) Influence of “loop” diuretics upon Na+,K+-ATPase and adenylate cyclase of the stria vascularis. Arch Otorhinolaryngol 217:347–359
Pettinger WA, Umemura S, Smith DD, Jeffries WB (1987) Renal α2-adrenoreceptors and the adenylate cyclase - cAMP system: biochemical and physiological interactions. Am J Physiol 252: F199-F208
Schacht J (1985) Hormonal regulation of adenylate cyclase in the stria vascularis of the mouse. Hear Res 20:9–13
Schlondorff D, Carvounis CP, Jacoby M, Satriano JA, Levine SD (1981) Multiple sites for interaction of prostaglandin and vasopressin in toad urinary bladder. Am J Physiol 241: F625-F631
Snedecor GW, Cochran WG (1967) Statistical methods, 6th edn. Iowa, State Univesity Press, Ames
Steiner AL, Pagliara AS, Chase LR, Kipnis DM (1972) Radioimmunoassay for cyclic nucleotides. II. Adenosine 3′-5′ monophosphate and guanosine 3′-5′ monophosphate in mammalian tissues and body fluids. J Biol Chem 247:1114–1120
Sterkers O, Ferrary E, Amiel C (1988) Production of inner ear fluids. Physiol Rev 68:1083–1128
Tran Ba Huy P, Servin F, Ohresser M, Kuntziger H (1981) Adenylate cyclase in guinea pig stria vascularis. Acta Otolaryngol (Stockh) 91:9–14
Zajic G, Anniko M, Schacht J (1983) Cellular localization of adenylate cyclase in the developing and mature inner ear of the mouse. Hear Res 10:249–261
Zenner HP, Zenner B (1979) Vasopressin and isoproterenol activate adenylate cyclase in the guinea pig inner ear. Arch Otorhinolaryngol 222:275–283
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Offprint requests to: E. Ferrary, INSERM U.251, Faculté de Médecine Xavier Bichat, 16, rue Henri Huchard, F-75018 Paris, France
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Ferrary, E., Bernard, C., Friedlander, G. et al. Antidiuretic hormone stimulation of adenylate cyclase in semicircular canal epithelium. Eur Arch Otorhinolaryngol 248, 275–278 (1991). https://doi.org/10.1007/BF00176754
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DOI: https://doi.org/10.1007/BF00176754