Abstract
1 By means of the double sucrose-gap technique, the effects of bradykinin and the bradykinin potentiating peptide BPP5a were compared on the guinea-pig taenia coli under a number of experimental conditions.
2 In normal Krebs solution the response to bradykinin was mostly a slight stimulation, characterized by a depolarization, an increase in spontaneous spike activity and a contraction. If BPP5a caused any effect at all, it was stimulation of the spike activity but without depolarization. Since the effect of bradykinin was little affected by an increase in dose, a potentiating effect of BPP5a could not be determined.
3 Spontaneous spikes with a 5 to 7 s rhythm and prepotentials at their base were inhibited by bradykinin, whereas they were stimulated by BPP5a.
4 Oscillatory potentials (slow waves) induced by a calcium and magnesium-free medium were also suppressed by bradykinin and stimulated by BPP5a. This effect of bradykinin was accompanied by a depolarization and a decrease in membrane resistance, phenomena not found after administration of BPP5a.
5 The amplitude of spontaneous spikes induced by potassium-depolarization was suppressed by bradykinin, even though the membrane resistance and potential had been decreased. BPP5a produced either no effect or a small stimulatory effect without influencing the membrane resistance.
6 Reduction of the calcium concentration to 0.25 mM enhanced the stimulatory responses to both bradykinin and BPP5a, especially the spike activity and depolarization. In this case the membrane resistance was increased by bradykinin as well as BPP5a. These effects, especially those of BPP5a, were inhibited by reduction of the sodium concentration to 15.5 mM. Reduction of the chloride concentration to 9.7 mM decreased rather than increased the stimulatory effects of both bradykinin and BPP5a. Under these conditions bradykinin did not decrease the membrane resistance.
7 Bradykinin can have both inhibitory and stimulatory effects on the taenia coli whereas BPP5a has only a stimulatory effect. Since under certain conditions both responses to bradykinin are accompanied by a sodium-dependent depolarization and decrease in membrane resistance, not influenced by lanthanum to any extent, it is suggested that bradykinin induces an increase in sodium conductance of the membrane. Under all the conditions investigated, except in low calcium, BPP5a did not affect the membrane potential and resistance. Thus, the underlying cause of its stimulatory effect is probably different from that of bradykinin.
Full text
PDF









Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aarsen P. N., van Caspel-de Bruyn M. Effect of changes in ionic environment on the action of bradykinin on the guinea-pig taenia coli. Eur J Pharmacol. 1970;12(3):348–358. doi: 10.1016/0014-2999(70)90087-7. [DOI] [PubMed] [Google Scholar]
- Bauer G., Ziegler E., Konzett H. Zur Hemmwirkung von Kininen an isolierten Darmpräparaten. Naunyn Schmiedebergs Arch Pharmakol Exp Pathol. 1966;254(3):235–244. [PubMed] [Google Scholar]
- Bolton T. B. Effects of stimulating the acetylcholine receptor on the current-voltage relationships of the smooth muscle membrane studied by voltage clamp of potential recorded by micro-electrode. J Physiol. 1975 Aug;250(1):175–202. doi: 10.1113/jphysiol.1975.sp011048. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bolton T. B. On the nature of the oscillations of the membrane potential (slow waves) produced by acetylcholine or carbachol in intestinal smooth muscle. J Physiol. 1971 Jul;216(2):403–418. doi: 10.1113/jphysiol.1971.sp009532. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brading A., Bülbring E., Tomita T. The effect of sodium and calcium on the action potential of the smooth muscle of the guinea-pig taenia coli. J Physiol. 1969 Feb;200(3):637–654. doi: 10.1113/jphysiol.1969.sp008713. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bülbring E., Tomita T. Effects of Ca removal on the smooth muscle of the guinea-pig taenia coli. J Physiol. 1970 Sep;210(1):217–232. doi: 10.1113/jphysiol.1970.sp009205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bülbring E., Tomita T. Increase of membrane conductance by adrenaline in the smooth muscle of guinea-pig taenia coli. Proc R Soc Lond B Biol Sci. 1969 Mar 11;172(1027):89–102. doi: 10.1098/rspb.1969.0013. [DOI] [PubMed] [Google Scholar]
- Camargo A., Ferreira S. H. Action of bradykinin potentiating factor (BPF) and dimercaprol (BAL) on the responses to bradykinin of isolated preparations of rat intestines. Br J Pharmacol. 1971 Jun;42(2):305–307. doi: 10.1111/j.1476-5381.1971.tb07113.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casteels R., Kuriyama H. Membrane potential and ion content in the smooth muscle of the guinea-pig's taenia coli at different external potassium concentrations. J Physiol. 1966 May;184(1):120–130. doi: 10.1113/jphysiol.1966.sp007906. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DAY M., VANE J. R. An analysis of the direct and indirect actions of drugs on the isolated guinea-pig ileum. Br J Pharmacol Chemother. 1963 Feb;20:150–170. doi: 10.1111/j.1476-5381.1963.tb01306.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ELLIOTT D. F., HORTON E. W., LEWIS G. P. Actions of pure bradykinin. J Physiol. 1960 Oct;153:473–480. doi: 10.1113/jphysiol.1960.sp006548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gershon M. D. Effects of tetrodotoxin on innervated smooth muscle preparations. Br J Pharmacol Chemother. 1967 Mar;29(3):259–279. doi: 10.1111/j.1476-5381.1967.tb01958.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Golenhofen K., Petrányi P. Spikes of smooth muscle in calcium-free solution (isolated taenia coli of the guinea pig). Experientia. 1969 Mar 15;25(3):271–273. doi: 10.1007/BF02034386. [DOI] [PubMed] [Google Scholar]
- HORTON E. W. Human urinary kinin excretion. Br J Pharmacol Chemother. 1959 Mar;14(1):125–132. doi: 10.1111/j.1476-5381.1959.tb00938.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hall D. W., Bonta I. L. The biphasic response of the isolated guinea-pig ileum by bradykinin. Eur J Pharmacol. 1973 Feb;21(2):147–154. doi: 10.1016/0014-2999(73)90219-7. [DOI] [PubMed] [Google Scholar]
- Mayer C. J., van Breemen C., Casteels T. The action of lanthanum and D600 on the calcium exchange in the smooth muscle cells of the guinea-pig Taenia coli. Pflugers Arch. 1972;337(4):333–350. doi: 10.1007/BF00586650. [DOI] [PubMed] [Google Scholar]
- Ohashi H., Nonomura Y., Oga A. Effects of angiotensin, bradykinin and oxytocin on electrical and mechanical activities in the taenia coli of the guinea pig. Jpn J Pharmacol. 1967 Jun;17(2):247–257. doi: 10.1254/jjp.17.247. [DOI] [PubMed] [Google Scholar]
- STURMER E., BERDE B. A comparative pharmacological study of synthetic eledoisin and synthetic bradykinin. J Pharmacol Exp Ther. 1963 Jun;140:349–355. [PubMed] [Google Scholar]
- Shimo Y., Holland W. C. Effects of potassium on membrane potential, spike discharge, and tension in taenia coli. Am J Physiol. 1966 Dec;211(6):1299–1304. doi: 10.1152/ajplegacy.1966.211.6.1299. [DOI] [PubMed] [Google Scholar]
- Szurszewski J. H., Bülbring E. The stimulant action of acetylcholine and catecholamines on the uterus. Philos Trans R Soc Lond B Biol Sci. 1973 Mar 15;265(867):149–156. doi: 10.1098/rstb.1973.0017. [DOI] [PubMed] [Google Scholar]
- Ufkes J. G., Aarsen P. N., Van Der Meer C. The bradykinin potentiating activity of two pentapeptides on various isolated smooth muscle preparations. Eur J Pharmacol. 1976 Nov;40(1):137–144. doi: 10.1016/0014-2999(76)90363-0. [DOI] [PubMed] [Google Scholar]
- Weiss G. B., Goodman F. R. Effects of lanthanum on contraction, calcium distribution and Ca45 movements in intestinal smooth muscle. J Pharmacol Exp Ther. 1969 Sep;169(1):46–55. [PubMed] [Google Scholar]
