Pre- and post-synaptic muscarinic receptors in thin slices of rat adrenal gland

被引:20
作者
Barbara, JG [1 ]
Lemos, VS [1 ]
Takeda, K [1 ]
机构
[1] Univ Louis Pasteur Strasbourg 1, CNRS URA600, Lab Pharmacol & Physiopathol Cellulaires, F-67401 Illkirch Graffenstaden, France
关键词
BK channels; chromaffin cell; fura-2; internal calcium; synaptic currents;
D O I
10.1046/j.1460-9568.1998.00349.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of activation of muscarinic receptors on chromaffin cells and splanchnic nerve terminals were studied in a rat adrenal slice preparation. In chromaffin cells, muscarine induced a transient hyperpolarization followed by a depolarization associated with cell spiking. The hyperpolarization was blocked by charybdotoxin (1 mu M) and tetraethylammonium chloride (TEA, 1 mM), but was not affected by 200 mu M Cd2+ or removal of external Ca2+ consistent with activation of BK channels. This would follow internal Ca2+ mobilization, as shown by Ca2+ imaging with fura-2 on isolated chromaffin cells in culture. Under voltage-clamp, outward BK currents were insensitive to MT3 toxin, a specific muscarinic m4 receptor antagonist. In contrast, muscarine-induced depolarization was due to a m4 receptor-mediated inward current blocked by MT3 toxin. This current was permeable to cations and was associated with Ca2+ entry and subsequently, Ca2+-induced Ca2+ release. Finally, both muscarine (25 mu M) and oxotremorine (10 mu M) decreased the amplitude and frequency of KCl-evoked excitatory postsynaptic currents, without affecting quantal size, consistent with a presynaptic inhibitory effect. Taken together, our data suggest that activation of m4 and probably m3 muscarinic receptors results in a strong, long-lasting excitation of chromaffin cells, as well as an uncoupling of synaptic inputs onto these cells.
引用
收藏
页码:3535 / 3545
页数:11
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