Abstract
1 The effect of tetraphenylboron (TPB) were studied on the frog sciatic nerve-sartorius muscle preparation. 2 TPB (0.01-1 mM) blocked indirectly elicited twitches of the preparation. 3 TPB (0.01-0.1 mM) produced no depolarization but lowered membrane resistance. TPB increased miniature endplate potential (m.e.p.p.) frequency, the rate of rise of the endplate potential (e.p.p.), and slowed the rate of rise and rate of fall of the muscle action potential. 4 In Mg2+ solutions the quantal content of e.p.ps was initially increased by TPB (0.01 mM). This was followed by a decrease of e.p.p. and m.e.p.p. amplitudes, accompanied by a lack of e.p.p. failures. 5 Larger concentrations of TPB (0.1 mM) produced an increase in e.p.p. amplitude followed by the sudden abolition of e.p.ps. This effect was associated with abolition of the nerve terminal spike. 6 TPB (0.1 mM) exhibited no postjunctional blocking action. 7 The results indicate that TPB acts prejunctionally, initially causing an increased release of acetylcholine. Subsequently, transmitter output is reduced by a reduction of quantal size.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- AUGUSTINSSON K. B., GRAHN M. The occurrence of choline esters in the honeybee. Acta Physiol Scand. 1954 Nov;32(2-3):174–190. doi: 10.1111/j.1748-1716.1954.tb01165.x. [DOI] [PubMed] [Google Scholar]
- Akiyama T., Grundfest H. The hyperpolarization of frog skeletal muscle fibres induced by removing potassium from the bathing medium. J Physiol. 1971 Aug;217(1):33–60. doi: 10.1113/jphysiol.1971.sp009558. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DEL CASTILLO J., KATZ B. Quantal components of the end-plate potential. J Physiol. 1954 Jun 28;124(3):560–573. doi: 10.1113/jphysiol.1954.sp005129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guideri G., Seifter E., Seifter J. Effects of a negative quaternary ion-sodium tetraphenylboron (TPB) on the rat phrenic nerve-diaphragm preparation. Eur J Pharmacol. 1972 Feb;17(2):253–258. doi: 10.1016/0014-2999(72)90166-5. [DOI] [PubMed] [Google Scholar]
- Johnson E. W., Parsons R. L. Characteristics of postjunctional carbamylcholine receptor activation and inhibition. Am J Physiol. 1972 Mar;222(3):793–799. doi: 10.1152/ajplegacy.1972.222.3.793. [DOI] [PubMed] [Google Scholar]
- Manthey A. A. The effect of calcium on the desensitization of membrane receptors at the neuromuscular junction. J Gen Physiol. 1966 May;49(5):963–976. doi: 10.1085/jgp.49.5.963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marshall I. G. Actions of tetraphenylboron on neuromuscular transmission in the biventer cervicis muscle of the chick. Eur J Pharmacol. 1970;13(1):51–54. doi: 10.1016/0014-2999(70)90181-0. [DOI] [PubMed] [Google Scholar]
- Miledi R., Thies R. Tetanic and post-tetanic rise in frequency of miniature end-plate potentials in low-calcium solutions. J Physiol. 1971 Jan;212(1):245–257. doi: 10.1113/jphysiol.1971.sp009320. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rappaport C., Howze G. B. Dissociation of adult mouse liver by sodium tetraphenylboron, a potassium complexing agent. Proc Soc Exp Biol Med. 1966 Apr;121(4):1010–1016. doi: 10.3181/00379727-121-30951. [DOI] [PubMed] [Google Scholar]
- Utsumi K., Packer L. Uncoupling of energy transfer reactions in mitochondria by tetraphenyl boron. Arch Biochem Biophys. 1967 Nov;122(2):509–515. doi: 10.1016/0003-9861(67)90226-3. [DOI] [PubMed] [Google Scholar]
