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胰蛋白酶和其他一些蛋白水解酶对豚鼠心脏的正性肌力和变时作用。

Positive inotropic and chronotropic effects of trypsin and some other proteolytic enzymes in the guinea-pig heart.

作者信息

Imai S, Kawada T, Kimura T, Ohta H, Nakazawa M, Yoshida Y

机构信息

Department of Pharmacology, Niigata University School of Medicine, Japan.

出版信息

Br J Pharmacol. 1987 Sep;92(1):55-62. doi: 10.1111/j.1476-5381.1987.tb11295.x.

Abstract

1 In atrial preparations of the young guinea-pig (body weight 150-250 g), five proteolytic enzymes (trypsin, chymotrypsin, bacterial-Al-proteinase (nagarse), bromelain and kallikrein) produced concentration-dependent positive inotropic and chronotropic effects, while they exerted only minimal effects on the papillary muscle preparations. 2 To characterize the effects, further experiments were conducted in atrial preparations using trypsin. There was a strong tendency for tachyphylaxis: a second exposure to the same concentration of trypsin resulted in considerably smaller positive inotropic and chronotropic effects. The positive inotropic and chronotropic effects of this substance were not affected by propranolol (5 X 10(-7)M). However, an accumulation of cyclic AMP was observed and the positive inotropic and chronotropic effects were potentiated by aminophylline (10(-4)M) in association with an augmentation of the accumulation of cyclic AMP. In preparations partially depolarized with high K+ (22mM) medium (contractions ceased under this condition) trypsin 100 micrograms ml-1 reinstated the contraction. Treatment of the preparation with aprotinin (200 u ml-1) resulted in a strong inhibition of the positive inotropic and chronotropic effects. 3 Islet activating protein (IAP), a specific inhibitor of the 'inhibition specific' guanine nucleotide binding regulatory protein of the adenylate cyclase system, did not produce significant inhibition of the positive inotropic and chronotropic effects of trypsin, whereas it produced a complete inhibition of the negative inotropic and chronotropic effects of carbachol. 4. These results suggest that the positive inotropic and chronotropic effects ofproteolytic enzymes are intimately connected with the proteolytic activities through which adenylate cyclase is activated to produce an accumulation of cyclic AMP within the myocardium. The destruction of the 'inhibition specific' guanine nucleotide regulatory protein of the adenylate cyclase was not substantiated as a mechanism of activation of the adenylate cyclase.

摘要
  1. 在幼年豚鼠(体重150 - 250克)的心房标本中,五种蛋白水解酶(胰蛋白酶、糜蛋白酶、细菌碱性蛋白酶(纳加酶)、菠萝蛋白酶和激肽释放酶)产生浓度依赖性的正性变力和变时作用,而它们对乳头肌标本的作用极小。2. 为了表征这些作用,使用胰蛋白酶在心房标本中进行了进一步实验。快速耐受有很强的倾向:再次暴露于相同浓度的胰蛋白酶会导致正性变力和变时作用明显减小。该物质的正性变力和变时作用不受普萘洛尔(5×10⁻⁷M)影响。然而,观察到环磷酸腺苷(cAMP)积累,并且氨茶碱(10⁻⁴M)与cAMP积累增加相关联,增强了正性变力和变时作用。在用高钾(22mM)培养基部分去极化的标本中(在此条件下收缩停止),100微克/毫升的胰蛋白酶恢复了收缩。用抑肽酶(200单位/毫升)处理标本导致正性变力和变时作用强烈抑制。3. 胰岛激活蛋白(IAP),一种腺苷酸环化酶系统“抑制特异性”鸟嘌呤核苷酸结合调节蛋白的特异性抑制剂,并不能显著抑制胰蛋白酶的正性变力和变时作用,而它能完全抑制卡巴胆碱的负性变力和变时作用。4. 这些结果表明,蛋白水解酶的正性变力和变时作用与蛋白水解活性密切相关,通过该活性腺苷酸环化酶被激活,从而在心肌内产生cAMP积累。腺苷酸环化酶“抑制特异性”鸟嘌呤核苷酸调节蛋白的破坏并未被证实是腺苷酸环化酶激活的机制。

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