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大鼠肝实质中的NADP依赖性脱氢酶。II. 葡萄糖-6-磷酸脱氢酶定性和定量分布模式的比较,特别提及性别差异。

NADP-dependent dehydrogenases in rat liver parenchyma. II. Comparison of qualitative and quantitative G6PDH distribution patterns with particular reference to sex differences.

作者信息

Teutsch H F, Rieder H

出版信息

Histochemistry. 1979 Feb 26;60(1):43-52. doi: 10.1007/BF00495727.

Abstract

Qualitative histochemical G6PDH distribution patterns obtained in the liver acinus of adult male and female rats with an improved method (Rieder et al., 1978) served as a basis for the isolation by microdissection of tissue samples of defined zonal affiliation. G6PDH activity was assayed quantitatively in tissue samples of zones 1 and 3 by a microfluorometric method, using the oil well technique and enzymatic cycling (Burch et al., 1963; Lowry and Passonneau, 1972). With the use of a correlation system further evidence could be presented for the validity of the recently described qualitative distribution patterns. From a total of 50 analyzed tissue samples the following G6PDH activities were calculated: 4.25 +/- 1.56 U/g dry weight in zone 1 and 2.08 +/- 0.46 U/g dry weight in zone 3 of male and 7.21 +/- 1.03 U/g dry weight in zone 1 and 11.10 +/- 2.56 U/g dry weight in zone 3 of female rats. These data were corrected for interference from the G6PDH activity of the Kupffer cells within zone 1 samples (approximately 80 U/g dry weight), so that the actual relative values for the parenchymal activity could be estimated for the first time: 2 U/g dry weight in zones 1 and 3 of male animals, 5 U/g dry weight in zone 1 and 11 U/g dry weight in zone 3 of female animals. In female livers G6PDH activity in zone 1 is therefore 2.5 times higher, and in zone 3 5 times higher than in the male. These zonal as well as sex-differences are clearly indicative of a heterogeneous functional organization of the liver acinus in terms of capacity for NADPH production, mainly in connection with reductive reactions in fatty acid synthesis.

摘要

采用改良方法(里德等人,1978年)在成年雄性和雌性大鼠肝腺泡中获得的定性组织化学G6PDH分布模式,为通过显微切割分离具有明确区域归属的组织样本奠定了基础。使用油井技术和酶循环,通过显微荧光法对1区和3区的组织样本进行G6PDH活性定量测定(伯奇等人,1963年;洛瑞和帕索诺,1972年)。通过使用相关系统,可以为最近描述的定性分布模式的有效性提供进一步证据。从总共50个分析的组织样本中计算出以下G6PDH活性:雄性大鼠1区为4.25±1.56 U/g干重,3区为2.08±0.46 U/g干重;雌性大鼠1区为7.21±1.03 U/g干重,3区为11.10±2.56 U/g干重。对1区样本中库普弗细胞的G6PDH活性干扰(约80 U/g干重)进行了校正,从而首次估计了实质活性的实际相对值:雄性动物1区和3区为2 U/g干重,雌性动物1区为5 U/g干重,3区为11 U/g干重。因此,在雌性肝脏中,1区的G6PDH活性比雄性高2.5倍,3区比雄性高5倍。这些区域差异以及性别差异清楚地表明,就NADPH产生能力而言,肝腺泡存在异质性功能组织,这主要与脂肪酸合成中的还原反应有关。

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