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兰尼碱对去垢剂处理的心肌细胞的作用。

Effects of ryanodine in skinned cardiac cells.

作者信息

Fabiato A

出版信息

Fed Proc. 1985 Dec;44(15):2970-6.

PMID:2415405
Abstract

Ryanodine (1 X 10(-5) M) did not affect the Ca2+ sensitivity of the myofilaments of skinned (sarcolemma removed by microdissection) cardiac cells from the rat ventricle. Ryanodine (1 X 10(-5) M) inhibited three types of Ca2+ release from the sarcoplasmic reticulum (SR), which have different mechanisms: 1) Ca2+-induced release of Ca2+ triggered by a rapid and transient increase of [free Ca2+] at the outer surface of the SR; 2) caffeine-induced release of Ca2+; 3) spontaneous cyclic release of Ca2+ occurring in the continuous presence of a [free Ca2+] sufficient to overload the SR. These results suggest that the three types of Ca2+ release are through the same channel across the SR membrane, although the gating mechanisms are different for the three types. Ryanodine also diminished the rate of Ca2+ accumulation into the SR. Even in the presence of 1 X 10(-5) M ryanodine the SR accumulated Ca2+ that could be released when the SR was sufficiently overloaded with Ca2+. Thus, ryanodine pretreatment did not permit the direct activation of the myofilaments by externally applied Ca2+. The approximately 1000-fold difference in the effective concentrations of ryanodine in intact vs. skinned cardiac cells suggests that low concentrations of ryanodine act in the intact cardiac tissues through processes or on structures that are destroyed by the skinning procedure. No significant differences were observed in the effects of ryanodine in skinned cardiac cells from different adult mammalian species.

摘要

ryanodine(1×10⁻⁵M)对大鼠心室去膜(通过显微解剖去除肌膜)心肌细胞肌丝的Ca²⁺敏感性没有影响。ryanodine(1×10⁻⁵M)抑制了肌浆网(SR)三种不同机制的Ca²⁺释放:1)由SR外表面[游离Ca²⁺]快速短暂升高触发的Ca²⁺诱导的Ca²⁺释放;2)咖啡因诱导的Ca²⁺释放;3)在[游离Ca²⁺]持续存在足以使SR过载的情况下发生的自发周期性Ca²⁺释放。这些结果表明,尽管三种类型的门控机制不同,但三种类型的Ca²⁺释放是通过SR膜上的同一通道。Ryanodine也降低了Ca²⁺积累到SR中的速率。即使存在1×10⁻⁵M的ryanodine,当SR被Ca²⁺充分过载时,SR仍能积累可释放的Ca²⁺。因此,ryanodine预处理不允许通过外部施加Ca²⁺直接激活肌丝。完整心肌细胞与去膜心肌细胞中ryanodine有效浓度相差约1000倍,这表明低浓度的ryanodine在完整心肌组织中的作用是通过去皮程序破坏的过程或结构来实现的。在不同成年哺乳动物物种的去膜心肌细胞中,未观察到ryanodine作用的显著差异。

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