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溶血磷脂酸对大鼠心肌细胞膜Na+-Ca2+交换的影响

Influence of lysophosphatidic acid on Na+-Ca2+ exchange activity in rat cardiac sarcolemma

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【作者】 刘乃奎杨军董林旺庞永正苏静怡唐朝枢

【Author】 LIU Nai-kui;YANG Jun;DONG Lin-wang (Institute of Cardiovascular Research, The first Hopital Beijing Medical University, Beijing 100034, China)

【机构】 北京医科大学第一医院心血管研究所!北京100034北京医科大学第一医院心血管研究所!北

【摘要】 本研究采用蔗糖梯度离心法制各大鼠心肌细胞膜,观察溶血磷脂酸( LPA)对心肌细胞膜 Na-Ca2+交换的影 响。结果发现LPA(1~20nmol/L)呈剂量依赖性和时间依赖性刺激Na一Ca2+交换活性增加。Gpp(NH)p呈剂量依赖 性替代LPA刺激的Na-Ca2+交换活性;PTX可抑制LPA对Na-Ca2+交换的激活;Genistein,Propranolol,Prazosin,Atropine,Losartan,BQ123和磷脂酰胆碱对LPA诱导的Na-Ca+交换活性无影响,而磷脂酰丝氨酸可增加对照和LPA 两组的 Na-Ca2+交换活性。这些结果表明 LPA可通过 PTX敏感的 G蛋白刺激大鼠心肌细胞膜 Na-Ca2+交换活性。

【Abstract】 Sprague-Dawley rat cardiac sarcolemmal membrane was prepared by the sucrose gradient centrifugation and Influence of Lysophosphatidic acid (LPA ) on Na~+-Ca~2+ exchange activity in rat cardiac sarcolemma was investigated. The results showed that LPA stimulated Na~+-Ca~2+ exchange activity in a dose-dependent manner from 1-20nmol/L and LPA-stimulated Na~+-Ca~2+ exchange activity increased with time and to the maximum at about 5 see. Activation of Na~+Ca~2+ exchange by LPA was displaced by Gpp(NH)p in dose-dependent manner. The activation of Na~+-Ca~2+ exchange by LPA was inhibited by pertussis (PTX). LPA-induced Na~+-Ca~2+ exchange activity was not affected by Genistein, Propranolol, Prazosin, Atropine, Losartan or BQ123. Phospholipid phosphatedylserine increased Na~+-Ca~2+ exchange activity in both control group and LPA treated group while phospholipid phosphatidylserine increased Na~+-Ca~2+ exchange activity in both control group and LPA treated group while phospholipid phosphatidylcholine did not significantly affect Na~+-Ca~2+ exchange activity in both groups. These findings indicate that LPA stimulates Na~+-Ca~2+ exchange activity in rat heart sarcolemma by a PTX-sensitive G protein. The activation of Na~+-Ca~2+ exchange by LPA is associated with the membrane phospholipid and is not related to tyrosine protein kinase, β-adrenoceptor, α,-adrenoceptor, muscarinic receptor, angiotensin Ⅱ receptor (AT1 ) and endothelin A receptor.

  • 【文献出处】 基础医学与临床 ,BASIC MEDICAL SCIENCES AND CLINICS , 编辑部邮箱 ,2000年02期
  • 【分类号】R331.3
  • 【被引频次】8
  • 【下载频次】72
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