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在豚鼠胃窦环形肌和兔门静脉中,经雷诺丁处理后咖啡因产生的持续性收缩。

Sustained contraction produced by caffeine after ryanodine treatment in the circular muscle of the guinea-pig gastric antrum and rabbit portal vein.

作者信息

Chowdhury J U, Pang Y W, Huang S M, Tsugeno M, Tomita T

机构信息

Department of Physiology, School of Medicine, Nagoya University, Japan.

出版信息

Br J Pharmacol. 1995 Apr;114(7):1414-8. doi: 10.1111/j.1476-5381.1995.tb13363.x.

Abstract
  1. Caffeine inhibited spontaneous mechanical activity at 0.3-1 mM, but produced a tonic contraction at concentrations higher than 3 mM in the circular muscle of the guinea-pig gastric antrum. In the circular muscle of the rabbit portal vein, caffeine at concentrations higher than 1 mM produced an early phasic contraction followed by a small tonic component. The caffeine-induced contraction was abolished by removal of the external Ca2+ more rapidly in the gastric antrum than the portal vein. 2. When the preparations were pretreated with ryanodine (1 microM) a sustained contraction developed on wash-out of caffeine (10 mM) both in the gastric antrum and portal vein. This contraction was not affected by nicardipine (3 microM) or verapamil (3 microM), but was readily abolished by removal of the external Ca2+ or by addition of cobalt (1 mM). Spontaneous electrical activity, the slow wave, in gastric muscles was blocked in the presence of 10 mM caffeine, but reappeared during the sustained contraction. 3. Both the contractions induced directly by caffeine and those produced following caffeine wash-out after ryanodine treatment were accompanied by a maintained increase in intracellular Ca2+ concentration measured with fura-2. 4. The presence or absence of Ca2+ during the application of ryanodine did not affect the ability of caffeine to initiate sustained contractions, provided Ca2+ was present during the exposure to caffeine. 5. It is concluded that caffeine can induce a sustained contraction after ryanodine treatment both in the guinea-pig gastric antrum and rabbit portal vein, by activating a Ca2+ influx pathway insensitive to organic Ca2+ channel blockers. No clear evidence was obtained for involvement of the Ca2+ influx pathway activated through depletion of intracellular Ca2+ stores. A hypothesis is proposed that the plasma membrane of these preparations is similar to the sarcoplasmic reticulum membrane in that Ca2+permeability can be increased almost irreversibly by a combination of caffeine and ryanodine in the presence of the external Ca2+.
摘要
  1. 咖啡因在0.3 - 1 mM时抑制豚鼠胃窦环行肌的自发机械活动,但在浓度高于3 mM时产生强直收缩。在兔门静脉环行肌中,浓度高于1 mM的咖啡因会产生早期的相性收缩,随后是较小的强直成分。咖啡因诱导的收缩在胃窦中比在门静脉中更快地被去除细胞外Ca2+所消除。2. 当用ryanodine(1 microM)预处理标本时,在去除咖啡因(10 mM)后,胃窦和门静脉中均出现持续收缩。这种收缩不受尼卡地平(3 microM)或维拉帕米(3 microM)的影响,但通过去除细胞外Ca2+或添加钴(1 mM)可轻易消除。胃肌中的自发电活动,即慢波,在存在10 mM咖啡因时被阻断,但在持续收缩期间重新出现。3. 咖啡因直接诱导的收缩以及ryanodine处理后咖啡因洗脱产生的收缩,均伴随着用fura - 2测量的细胞内Ca2+浓度的持续升高。4. 在应用ryanodine期间Ca2+的存在与否不影响咖啡因引发持续收缩的能力,前提是在暴露于咖啡因期间存在Ca2+。5. 得出结论,咖啡因在ryanodine处理后可在豚鼠胃窦和兔门静脉中诱导持续收缩,通过激活对有机Ca2+通道阻滞剂不敏感的Ca2+内流途径。未获得明确证据表明通过耗尽细胞内Ca2+储存激活的Ca2+内流途径参与其中。提出一个假设,即这些标本的质膜类似于肌浆网膜,在细胞外Ca2+存在的情况下,咖啡因和ryanodine的组合可几乎不可逆地增加Ca2+通透性。

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