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急性给予马吲哚对成年小鼠脑能量代谢的影响。

Effects of acute administration of mazindol on brain energy metabolism in adult mice.

机构信息

1 Laboratório de Bioenergética, Programa de Pós-graduação em Ciências da Saúde, Universidade do Extremo Sul Catarinense, Criciúma, SC, Brazil.

2 Instituto Nacional de Ciência e Tecnologia Translacional em Medicina, Porto Alegre, RS, Brazil.

出版信息

Acta Neuropsychiatr. 2014 Jun;26(3):146-54. doi: 10.1017/neu.2013.43.

Abstract

OBJECTIVES

Mazindol is a sympathomimetic amine, widely used as an anorectic agent in the treatment of obesity. This drug causes psychostimulant effects because of its pharmacological profile similar to amphetamine, acting like a monoamine reuptake inhibitor. However, the mechanisms underlying the action of mazindol are still not clearly understood.

METHODS

Swiss mice received a single acute administration of mazindol (0.25, 1.25 and 2.5 mg/kg, ip) or saline. After 2 h, the animals were killed by decapitation; the brain was removed and used for the evaluation of activities of mitochondrial respiratory chain complexes, Krebs cycle enzymes and creatine kinase.

RESULTS

Acute administration of mazindol decreased complex I activity only in the hippocampus. Complex IV activity was increased in the cerebellum (2.5 mg/kg) and cerebral cortex (0.25 mg/kg). Citrate synthase activity was increased in the cerebellum (1.25 mg/kg) and cerebral cortex (1.25 mg/kg), and creatine kinase activity was increased in the cerebellum (1.25 mg/kg).

CONCLUSION

We suggest that the inhibition of complex I in the hippocampus only and activation of complex IV, citrate synthase and creatine kinase occurs because of a stimulus effect of mazindol in the central nervous system, which causes a direct impairment on energy metabolism.

摘要

目的

马吲哚是一种拟交感胺,作为一种厌食药广泛用于肥胖症的治疗。由于其药理学特性与安非他命相似,作为单胺再摄取抑制剂,该药物具有精神兴奋剂作用。然而,马吲哚作用的机制仍不清楚。

方法

瑞士小鼠单次接受马吲哚(0.25、1.25 和 2.5 mg/kg,ip)或生理盐水处理。2 小时后,通过断头处死动物,取出大脑用于评估线粒体呼吸链复合物、三羧酸循环酶和肌酸激酶的活性。

结果

马吲哚急性给药仅降低海马中的复合物 I 活性。复合物 IV 活性在小脑(2.5 mg/kg)和大脑皮层(0.25 mg/kg)中增加。柠檬酸合酶活性在小脑(1.25 mg/kg)和大脑皮层(1.25 mg/kg)中增加,肌酸激酶活性在小脑(1.25 mg/kg)中增加。

结论

我们认为,仅在海马中抑制复合物 I 以及在中枢神经系统中刺激马吲哚激活复合物 IV、柠檬酸合酶和肌酸激酶,可能导致能量代谢的直接损伤。

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