首页> 外文期刊>The Journal of Physiology >Drastic facilitation by alpha-latrotoxin of bovine chromaffin cell exocytosis without measurable enhancement of Ca2+ entry or (Ca2+)i.
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Drastic facilitation by alpha-latrotoxin of bovine chromaffin cell exocytosis without measurable enhancement of Ca2+ entry or (Ca2+)i.

机译:牛嗜铬细胞胞吐作用的α-latrotoxin的彻底促进作用,而Ca2 +进入或(Ca2 +)i的增加没有可测量的增强。

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1. Latrotoxin (LTX, 1-3 nM) caused a gradual increase of the spontaneous catecholamine release rate in bovine adrenal chromaffin cells superfused with normal Krebs-Hepes solution containing 2.5 mM Ca2+. Ca2+ removal abolished this effect. LTX enhanced also the secretory responses to high K+ (35 or 70 mM) and to acetylcholine (ACh, 30 microM). 2. The application of Ca2+ pulses to cells previously superfused with a 0 Ca2+ solution (Krebs-Hepes deprived of CaCl2) induced secretory responses that gradually reached 400-800 nA of catecholamines, provided that LTX was present. The responses to ACh or 35 mM K+ pulses (in the presence of Ca2+) were also enhanced by LTX, from around 100-200 nA to over 1000 nA. Though such enhancement remained in the presence of Ca2+ channel blockers, it disappeared upon the lowering of [Na+]o or in electroporated cells. 3. Using protocols similar to those of secretion, LTX did not enhance basal 45Ca2+ uptake, whole-cell Ca2+ currents or basal [Ca2+]i. In fact, LTX attenuated theK(+)- or ACh-evoked increases in 45Ca2+ uptake and [Ca2+]i. 4. It is proposed that the secretory response to brief periods of Ca2+ reintroductions is triggered by local subplasmalemmal Ca2+i transients, produced by the Na(+)-Ca2+ exchanger of the plasma membrane working in the reverse mode. This situation might be physiologically reproduced during ACh stimulation of chromaffin cells, which is followed by the firing of Na(+)-dependent action potentials.
机译:1. Latrotoxin(LTX,1-3 nM)导致与含有2.5 mM Ca2 +的正常Krebs-Hepes溶液融合的牛肾上腺嗜铬细胞的自发儿茶酚胺释放速率逐渐增加。去除Ca2 +消除了这种作用。 LTX还增强了对高K +(35或70 mM)和对乙酰胆碱(ACh,30 microM)的分泌反应。 2.将Ca2 +脉冲施加到先前已与0 Ca2 +溶液(不含CaCl2的Krebs-Hepes)融合的细胞上,只要存在LTX,其分泌反应便逐渐达到400-800 nA儿茶酚胺。 LTX还增强了对ACh或35 mM K +脉冲(在Ca2 +存在下)的响应,从大约100-200 nA到超过1000 nA。尽管这种增强在Ca2 +通道阻滞剂的存在下仍然存在,但在[Na +] o降低或在电穿孔细胞中消失。 3.使用与分泌相似的方案,LTX不会增强基础45Ca2 +吸收,全细胞Ca2 +电流或基础[Ca2 +] i。实际上,LTX减弱了45Ca2 +吸收和[Ca2 +] i引起的K(+)或ACh诱发的增加。 4.提出对Ca2 +短暂重新引入的分泌反应是由质膜的Na(+)-Ca2 +交换体以反向模式工作而产生的局部亚浆膜Ca2 + i瞬变触发的。这种情况可能是在ACh刺激嗜铬细胞的生理过程中重现的,其次是激发Na(+)依赖的动作电位。

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