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甲状腺激素对大鼠肝细胞内多余脂肪储存的直接影响。

Direct effects of iodothyronines on excess fat storage in rat hepatocytes.

机构信息

Dipartimento di Biologia, Università di Genova, Italy.

出版信息

J Hepatol. 2011 Jun;54(6):1230-6. doi: 10.1016/j.jhep.2010.09.027. Epub 2010 Nov 3.

Abstract

BACKGROUND & AIMS: Previous studies have demonstrated that 3,5-L-diiodothyronine (T(2)) is able to prevent lipid accumulation in the liver of rats fed a high-fat diet. Whether this effect is due to a direct action of T(2) on the liver has not been elucidated. In this study, we investigated the ability of T(2) to reduce the excess lipids in isolated hepatocytes treated with fatty acids (FFAs). The effects of T(2) were compared with those elicited by 3,3',5-L-triiodothyronine (T(3)).

METHODS

To mimic the fatty liver condition, primary cultures of rat hepatocytes were overloaded with lipids, by exposure to FFAs ("fatty hepatocytes"), and then treated with T(2) or T(3). Lipid content, morphometry of lipid droplets (LDs), and expression of the adipocyte differentiation-related protein (ADRP) and the peroxisome proliferator-activated receptors (PPAR-α, -γ, -δ) were evaluated. Activities of the lipolytic enzyme acyl CoA oxidase-AOX and the antioxidant enzymes superoxide dismutase-SOD and catalase-CAT were also determined.

RESULTS

FFA-induced lipid accumulation was associated with an increase in both number/size of LDs and expression of ADRP, PPAR-γ, and PPAR-δ/β mRNAs, as well as in the activities of AOX, SOD, and CAT. The addition of T(2) or T(3) to "fatty hepatocytes" resulted in a reduction in: (i) lipid content and LD diameter; (ii) PPAR-γ and PPAR-δ expression; (iii) activities of AOX and antioxidant enzymes.

CONCLUSIONS

These data demonstrate, for the first time, a direct action of both T(2) and T(3) in reducing the excess fat in cultured hepatocytes.

摘要

背景与目的

先前的研究表明,3,5-二碘甲状腺原氨酸(T(2))能够防止高脂肪饮食喂养的大鼠肝脏中的脂质积累。这种作用是否是由于 T(2)对肝脏的直接作用尚不清楚。在这项研究中,我们研究了 T(2)降低用脂肪酸(FFAs)处理的分离肝细胞中多余脂质的能力。将 T(2)的作用与 3,3',5-三碘甲状腺原氨酸(T(3))引起的作用进行了比较。

方法

为了模拟脂肪肝的情况,通过暴露于 FFAs(“脂肪性肝细胞”)使大鼠原代肝细胞超负荷脂质,然后用 T(2)或 T(3)处理。评估了脂质含量、脂质滴(LDs)的形态计量学以及脂肪细胞分化相关蛋白(ADRP)和过氧化物酶体增殖物激活受体(PPAR-α、-γ、-δ)的表达。还测定了脂解酶酰基辅酶 A 氧化酶-AOX 和抗氧化酶超氧化物歧化酶-SOD 和过氧化氢酶-CAT 的活性。

结果

FFA 诱导的脂质积累与 LD 数量/大小的增加以及 ADRP、PPAR-γ 和 PPAR-δ/β mRNA 的表达增加以及 AOX、SOD 和 CAT 的活性增加相关。将 T(2)或 T(3)添加到“脂肪性肝细胞”中会导致:(i)脂质含量和 LD 直径降低;(ii)PPAR-γ 和 PPAR-δ 的表达降低;(iii)AOX 和抗氧化酶的活性降低。

结论

这些数据首次表明,T(2)和 T(3)均可直接作用于培养的肝细胞以减少多余的脂肪。

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