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对乙酰氨基酚的代谢作用。在离体灌注大鼠肝脏中的研究。

Metabolic effects of acetaminophen. Studies in the isolated perfused rat liver.

作者信息

Itinose A M, Sakuno M L, Bracht A

机构信息

Laboratory of Liver Metabolism, University of Maringá, Brazil.

出版信息

Cell Biochem Funct. 1989 Oct;7(4):263-73. doi: 10.1002/cbf.290070405.

Abstract

The effects of acetaminophen on the metabolism of the isolated perfused rat liver were investigated. The following results were obtained: (1) Acetaminophen increased glucose release and glycolysis from endogenous glycogen (glycogenolysis). (2) Oxygen uptake, gluconeogenesis from either pyruvate or fructose and glycogen synthesis were inhibited. (3) In isolated rat liver mitochondria acetaminophen decreased state III and state IV respiration; it also decreased the ADP/O ratio and the respiratory control ratio. (4) The action of acetaminophen on glycogenolysis was not affected by N-acetylcysteine; this compound, however, increased glycogen synthesis. (5) The effects of acetaminophen are reversible. It was concluded that glycogen depletion by acetaminophen can be produced by two mechanisms. The first, as previously demonstrated by several workers, depends on irreversible binding of a reactive metabolite. The second, however, is reversible and depends primarily on an inhibition of mitochondrial energy metabolism.

摘要

研究了对乙酰氨基酚对离体灌注大鼠肝脏代谢的影响。获得了以下结果:(1) 对乙酰氨基酚增加了内源性糖原的葡萄糖释放和糖酵解(糖原分解)。(2) 氧摄取、丙酮酸或果糖的糖异生以及糖原合成受到抑制。(3) 在离体大鼠肝脏线粒体中,对乙酰氨基酚降低了状态III和状态IV呼吸;它还降低了ADP/O比和呼吸控制率。(4) 对乙酰氨基酚对糖原分解的作用不受N-乙酰半胱氨酸的影响;然而,该化合物增加了糖原合成。(5) 对乙酰氨基酚的作用是可逆的。得出的结论是,对乙酰氨基酚导致的糖原耗竭可通过两种机制产生。第一种,如先前几位研究者所证明的,取决于活性代谢物的不可逆结合。然而,第二种是可逆的,主要取决于线粒体能量代谢的抑制。

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