
Stimulation of Ca 2+ uptake into epididymal bull spermatozoa by analogues of amiloride
Author(s) -
BREITBART Haim,
CRAGOE Edward J.,
LARDY Henry A.
Publication year - 1990
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.1990.tb19257.x
Subject(s) - amiloride , stimulation , chemistry , calcium , biophysics , motility , endocrinology , medicine , diltiazem , calcium channel , voltage dependent calcium channel , sodium , biology , microbiology and biotechnology , organic chemistry
Certain amiloride analogues 3′,4′‐dichlorobenzamil 2′,4′‐dimethylbenzamil and α′,2′‐benzobenzamil hydrochloride (ATBB) stimulate calcium accumulation and motility by epididymal bovine spermatozoa. This stimulation can be seen at a range of 0.1–0.4 mM, while at higher concentration there is inhibition of calcium uptake by these amiloride analogues. The amiloride derivative 5‐(4‐chlorobenzyl)‐2′,4′‐dimethylbenzamil (CBDMB), which bears a 4‐chlorobenzyl substituent on the 5‐amino nitrogen atom, did not stimulate calcium uptake. The amiloride analogue 3′,4′‐dichlorobenzamil inhibits the Na + /Ca 2+ ‐exchange activity in isolated plasma membrane vesicles, and the stimulatory effect of 3′,4′‐dichlorobenzamil on calcium uptake into epididymal sperm could be seen in Na + ‐free medium. Thus, the stimulation of Ca 2+ accumulation in the cells caused by 3′,4′‐dichlorobenzamil is not a result of inhibiting the Na − ‐dependent Ca 2‐ clearance. There is no stimulation of Ca 2+ uptake into ejaculated cells by adding 3′,4′‐dichlorobenzamil, which is not due to the presence of the calcium‐transport inhibitor (caltrin) in these cells [Rufo, G. A., Schoff, P. K. & Lardy, H. A. (1984) J. Biol. Chem. 259 , 2547–2552]. The stimulatory effect of 3′,4′‐dichlorobenzamil on Ca 2+ uptake is inhibited by the voltage‐dependent Ca 2+ ‐channel blockers nifedipin and diltiazem. This indicates that the stimulation of Ca 2+ uptake by the amiloride analogues is due to the activation of a voltage‐dependent Ca 2+ channel of the plasma membrane.