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钙通道阻滞剂尼卡地平、达罗地平、PN - 200 - 110和硝苯地平对离体大鼠胰岛胰岛素释放的影响。

The effect of calcium-blockers nicardipine, darodipine, PN-200-110 and nifedipine on insulin release from isolated rat pancreatic islets.

作者信息

Al-Mahmood H A, el-Khatim M S, Gumaa K A, Thulesius O

出版信息

Acta Physiol Scand. 1986 Feb;126(2):295-8. doi: 10.1111/j.1748-1716.1986.tb07817.x.

DOI:10.1111/j.1748-1716.1986.tb07817.x
PMID:2939690
Abstract

The effect of the calcium-blockers nicardipine, darodipine, PN-200-110 on insulin release from pancreatic islets was studied using nifedipine as a reference compound. All drugs at a concentration of 10(-6)M significantly inhibited insulin release in response to both low (5.5 mM) and high (22 mM) glucose. The present observations support previous reports that calcium blockers of the dihydropyridine series are effective inhibitors of glucose-induced insulin release.

摘要

以硝苯地平作为参比化合物,研究了钙通道阻滞剂尼卡地平、达罗地平、PN - 200 - 110对胰岛胰岛素释放的影响。所有浓度为10(-6)M的药物均能显著抑制对低(5.5 mM)、高(22 mM)葡萄糖刺激的胰岛素释放。本研究结果支持此前的报道,即二氢吡啶类钙通道阻滞剂是葡萄糖诱导胰岛素释放的有效抑制剂。

相似文献

1
The effect of calcium-blockers nicardipine, darodipine, PN-200-110 and nifedipine on insulin release from isolated rat pancreatic islets.钙通道阻滞剂尼卡地平、达罗地平、PN - 200 - 110和硝苯地平对离体大鼠胰岛胰岛素释放的影响。
Acta Physiol Scand. 1986 Feb;126(2):295-8. doi: 10.1111/j.1748-1716.1986.tb07817.x.
2
Effects of the calcium-channel agonist CGP 28392 on insulin secretion from isolated rat islets of Langerhans.钙通道激动剂CGP 28392对离体大鼠胰岛胰岛素分泌的影响。
Biochem J. 1985 Nov 1;231(3):629-34. doi: 10.1042/bj2310629.
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[Calcium antagonists and glycoregulation: dissociated effects of nicardipine on vascular tonus and insulin secretion].[钙拮抗剂与糖调节:尼卡地平对血管张力和胰岛素分泌的不同作用]
Arch Mal Coeur Vaiss. 1985 Oct;78(11):1661-6.
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Inhibition of glucose-induced insulin secretion by calcium channel blocking drugs in-vitro but not in-vivo in the rat.钙通道阻滞剂在体外而非体内对大鼠葡萄糖诱导的胰岛素分泌具有抑制作用。
J Pharm Pharmacol. 1988 Jan;40(1):22-6. doi: 10.1111/j.2042-7158.1988.tb05143.x.
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Dissociated effects of nicardipine on vascular tone and insulin secretion.尼卡地平对血管张力和胰岛素分泌的解离作用。
J Cardiovasc Pharmacol. 1986 Jul-Aug;8(4):707-11.
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Effects of Ca2+ channel agonist-antagonist enantiomers of dihydropyridine 202791 on insulin release, 45Ca uptake and electrical activity in isolated pancreatic islets.二氢吡啶 202791 的 Ca2+ 通道激动剂 - 拮抗剂对映体对分离胰岛中胰岛素释放、45Ca 摄取及电活动的影响
Exp Physiol. 1990 Jul;75(4):547-58. doi: 10.1113/expphysiol.1990.sp003431.
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Periodicity of insulin secretion comprises multiple cycles with different duration in perfused rat islets.在灌注的大鼠胰岛中,胰岛素分泌的周期性包括多个持续时间不同的周期。
Diabetes Res Clin Pract. 1992 Jul;17(1):27-32. doi: 10.1016/0168-8227(92)90040-x.
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Effect of Ca++ channel blockers on energy level and stimulated insulin secretion in isolated rat islets of Langerhans.钙离子通道阻滞剂对离体大鼠胰岛能量水平及刺激胰岛素分泌的影响。
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The dihydropyridine derivative, Bay K 8644, enhances insulin secretion by isolated pancreatic islets.二氢吡啶衍生物Bay K 8644可增强分离的胰岛分泌胰岛素的能力。
Naunyn Schmiedebergs Arch Pharmacol. 1985 Jan;328(3):351-3. doi: 10.1007/BF00515566.

引用本文的文献

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Br J Pharmacol. 2014 Jun;171(12):3010-22. doi: 10.1111/bph.12622.
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Localized calcium influx in pancreatic beta-cells: its significance for Ca2+-dependent insulin secretion from the islets of Langerhans.胰腺β细胞中的局部钙内流:其对朗格汉斯胰岛中钙依赖性胰岛素分泌的意义。
Endocrine. 2000 Dec;13(3):251-62. doi: 10.1385/ENDO:13:3:251.
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Permeation and gating properties of the L-type calcium channel in mouse pancreatic beta cells.
小鼠胰腺β细胞中L型钙通道的渗透和门控特性
J Gen Physiol. 1993 May;101(5):767-97. doi: 10.1085/jgp.101.5.767.
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Nicardipine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy, in the treatment of angina pectoris, hypertension and related cardiovascular disorders.尼卡地平。对其治疗心绞痛、高血压及相关心血管疾病的药效学、药代动力学特性及治疗效果的综述。
Drugs. 1987 Apr;33(4):296-345. doi: 10.2165/00003495-198733040-00002.
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Isradipine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in cardiovascular disease.伊拉地平。对其药效学和药代动力学特性以及在心血管疾病治疗中的应用的综述。
Drugs. 1990 Jul;40(1):31-74. doi: 10.2165/00003495-199040010-00004.