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β-激动剂可增强小鼠血清和心室肌细胞中乳酸脱氢酶(LDH)的表达。

Beta-agonists enhance the lactic dehydrogenase (LDH) expression in serum and ventricular myocytes of mice.

作者信息

Kaundal M, Katoch S S, Sharma S

机构信息

Department of Biosciences, Himachal Pradesh University, Summer Hill, Shimla-171005, India.

出版信息

Acta Physiol Hung. 2007 Sep;94(3):249-59. doi: 10.1556/APhysiol.94.2007.3.9.

Abstract

Beta-agonists have skeletal muscle specific protein anabolic effects and are also known to cause cardiac hypertrophy. Changed total LDH and its isozymic patterns are conveniently employed for the detection of different pathophysiological states of the tissues. The purpose of this study is to confirm total LDH and its isozymic expression in ventricular tissue and serum in mice following oral administration of single but higher dose of isoproterenol (Iso) and clenbuterol (Cl) (100 mg/kg body wt. and 20 mg/kg body wt., respectively), after 4, 8 and 20 hours of drug administration. Mice heart witnessed increased total LDH levels with time. Serum on the other hand showed decline in total LDH concentrations at the initial points of the drug treatment. No doubt, total LDH expression increased towards 20th h post-drug treatment but this increase is mainly due to anaerobic isozymes, i.e. LDH4 and LDH5. The findings of the present study suggest that tissue damage is definitely caused by two beta-agonists after giving single dose for shorter time span (20 hours) and the impact of the damage varies from drug to drug. Increase in total LDH in serum is not due to release from heart but from some other tissues having anaerobic metabolism.

摘要

β-激动剂具有骨骼肌特异性蛋白合成代谢作用,且已知会导致心脏肥大。总乳酸脱氢酶(LDH)及其同工酶模式的变化可方便地用于检测组织的不同病理生理状态。本研究的目的是在口服单次但较高剂量的异丙肾上腺素(Iso)和克伦特罗(Cl)(分别为100mg/kg体重和20mg/kg体重)后4、8和20小时,证实小鼠心室组织和血清中总LDH及其同工酶的表达情况。小鼠心脏中总LDH水平随时间增加。另一方面,血清在药物治疗初期总LDH浓度下降。毫无疑问,药物治疗后至第20小时总LDH表达增加,但这种增加主要是由于无氧同工酶,即LDH4和LDH5。本研究结果表明,在短时间(20小时)给予单次剂量后,两种β-激动剂肯定会造成组织损伤,且损伤的影响因药物而异。血清中总LDH的增加并非源于心脏释放,而是来自其他具有无氧代谢的组织。

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