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db 动物和 ob 动物的肥胖会导致肝脏极低密度脂蛋白分泌受损以及载脂蛋白 B-48 和 B-100 的分泌差异。

Obesity in db and ob animals leads to impaired hepatic very low density lipoprotein secretion and differential secretion of apolipoprotein B-48 and B-100.

作者信息

Li X, Grundy S M, Patel S B

机构信息

Center for Human Nutrition, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235-9052, USA.

出版信息

J Lipid Res. 1997 Jul;38(7):1277-88.

PMID:9254055
Abstract

Dyslipidemia secondary to obesity is commonly observed in both animals and humans. As it has been hypothesized that obesity can result in overproduction of VLDL, leading to the subsequent dyslipidemia, we have examined the triglyceride and apoB secretion rates in vivo in obese C57BI/ KsJ db/db and C57BI/6J ob/ob mice and their lean littermates. In ob/ob animals, obesity resulted in significantly lower, not higher, triglyceride secretion rates in both males (3.94 +/- 0.49 mg/h per g liver vs. 5.45 +/- 0.29 mg/h per g liver in lean littermates, P < 0.001) and females (4.29 +/- 0.81 mg/h per g liver vs. 5.25 +/- 0.59 mg/h/g liver, P < 0.001). For db/db, the obese females did not show a statistically significant triglyceride secretion rate compared to their lean littermates. Only the male db/db animals showed a significantly higher triglyceride secretion rate compared with lean littermates (5.50 +/- 1.1 mg/h per g liver vs. 3.37 +/- 0.36 mg/h/g liver, P < 0.001). Examination of the apolipoprotein B (apoB) secretion rates showed that for ob/ob animals and db/db obese females, apoB48 secretion was significantly decreased compared to that of normal littermates, with a small increase in apoB-100 secretion. Total apoB secreted, however, was not increased. Our data further suggest that the predominant cause of the dyslipidemia under these conditions is a defect in removal of VLDL from the circulation.

摘要

肥胖继发的血脂异常在动物和人类中都很常见。由于据推测肥胖可导致极低密度脂蛋白(VLDL)产生过多,进而引发后续的血脂异常,我们检测了肥胖的C57BI/KsJ db/db和C57BI/6J ob/ob小鼠及其瘦的同窝小鼠体内甘油三酯和载脂蛋白B的分泌率。在ob/ob动物中,肥胖导致雄性(3.94±0.49毫克/小时每克肝脏,而瘦的同窝小鼠为5.45±0.29毫克/小时每克肝脏,P<0.001)和雌性(4.29±0.81毫克/小时每克肝脏,而瘦的同窝小鼠为5.25±0.59毫克/小时每克肝脏,P<0.001)的甘油三酯分泌率显著降低,而非升高。对于db/db小鼠,肥胖雌性与瘦的同窝小鼠相比,甘油三酯分泌率无统计学显著差异。只有雄性db/db动物与瘦的同窝小鼠相比,甘油三酯分泌率显著升高(5.50±1.1毫克/小时每克肝脏,而瘦的同窝小鼠为3.37±0.36毫克/小时每克肝脏,P<0.001)。对载脂蛋白B(apoB)分泌率的检测表明,对于ob/ob动物和db/db肥胖雌性,与正常同窝小鼠相比,apoB48分泌显著减少,而apoB-100分泌略有增加。然而,总的apoB分泌并未增加。我们的数据进一步表明,在这些情况下血脂异常的主要原因是循环中VLDL清除缺陷。

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