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钌红和镁离子部分抑制银离子诱导的青蛙骨骼肌肌浆网中钙的释放。

Ruthenium red and magnesium ion partially inhibit silver ion-induced release of calcium from sarcoplasmic reticulum of frog skeletal muscles.

作者信息

Oba T, Iwama H, Aoki T

机构信息

Department of Physiology, Nagoya City University Medical School, Japan.

出版信息

Jpn J Physiol. 1989;39(2):241-54. doi: 10.2170/jjphysiol.39.241.

Abstract

Effects of Ca2+-induced Ca2+ release blockers, ruthenium red (RR) and Mg2+, on Ag+-induced Ca2+ release were studied using skinned muscle fibers or fragmented heavy SR (HSR) prepared from frog muscle, and compared with those on caffeine-induced one. Exposure of the skinned fibers to 5 microM Ag+ produced a rapid and large contraction in the presence of 0.043 mM free Mg2+. When Mg2+ concentration was increased to 0.86 mM, Ag+ led to a large transient contraction, combined with a small tonic one. The transient component was completely blocked by high Mg2+ (3.64 mM), but the tonic one was not. Ca2+-ATPase activity was not stimulated by increase of Mg2+ from 0.86 to 3.64 mM. Ag+ and caffeine induced a rapid Ca2+ efflux from HSR in a dose-dependent manner. RR over a range from 1 to 10 microM dose-dependently inhibited the Ca2+ efflux induced by 10 microM Ag+. Despite increase of RR to 30 microM, however, further inhibition of the Ca2+ efflux was not produced any more (77.8 +/- 12.2% inhibition). A 10 mM caffeine-induced efflux of Ca2+ was blocked slightly by only 0.5 microM RR and almost completely by 3 microM. A slight inhibition (about 28%) of the Ca2+-ATPase activity was observed in the presence of 10 microM Ag+ in 0.5 mg SR protein/ml of medium. RR and caffeine did not affect the enzyme activity. These results indicate that frog SR could induce a rapid release of Ca2+ upon Ag+ and caffeine, suggesting that Ag+ may have two different binding sites to release Ca2+; one is on Ca2+-induced Ca2+ release channel and the other on RR-insensitive site.

摘要

利用从蛙肌制备的皮肤肌纤维或破碎的重肌质网(HSR),研究了Ca2+诱导的Ca2+释放阻滞剂钌红(RR)和Mg2+对Ag+诱导的Ca2+释放的影响,并与它们对咖啡因诱导的Ca2+释放的影响进行了比较。在存在0.043 mM游离Mg2+的情况下,将皮肤肌纤维暴露于5 microM Ag+会产生快速且大幅度的收缩。当Mg2+浓度增加到0.86 mM时,Ag+会导致大幅度的瞬态收缩,并伴有小幅度的强直性收缩。瞬态成分被高浓度Mg2+(3.64 mM)完全阻断,但强直性成分未被阻断。将Mg2+从0.86 mM增加到3.64 mM不会刺激Ca2+-ATP酶活性。Ag+和咖啡因以剂量依赖性方式诱导HSR中Ca2+的快速外流。在1至10 microM范围内,RR剂量依赖性地抑制由10 microM Ag+诱导的Ca2+外流。然而,尽管RR增加到30 microM,Ca2+外流的进一步抑制不再产生(抑制率为77.8 +/- 12.2%)。10 mM咖啡因诱导的Ca2+外流仅被0.5 microM RR轻微阻断,而被3 microM几乎完全阻断。在含有0.5 mg SR蛋白/ml培养基中存在10 microM Ag+的情况下,观察到Ca2+-ATP酶活性有轻微抑制(约28%)。RR和咖啡因不影响该酶活性。这些结果表明,蛙肌质网在Ag+和咖啡因作用下可诱导Ca2+的快速释放,提示Ag+可能有两个不同的结合位点来释放Ca2+;一个位于Ca2+诱导的Ca2+释放通道上,另一个位于RR不敏感位点上。

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