Srisowanna Naparee, Choijookhuu Narantsog, Yano Koichi, Batmunkh Baatarsuren, Ikenoue Makoto, Nhat Huynh Mai Nguyen, Yamaguchi Yuya, Hishikawa Yoshitaka
Department of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, University of Miyazaki, Miyazaki 889-1692, Japan.
Department of Surgery, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia.
Acta Histochem Cytochem. 2019 Aug 30;52(4):67-75. doi: 10.1267/ahc.19018. Epub 2019 Aug 27.
Fatty liver is common in men and post-menopausal women, suggesting that estrogen may be involved in liver lipid metabolism. The aim of this study is to be clear the role of estrogen and estrogen receptor alpha (ERα) in fat accumulation during liver regeneration using the 70% partial hepatectomy (PHX) model in male, female, ovariectomized (OVX) and E-treated OVX (OVX-E) rats. Liver tissues were sampled at 0-48 hr after PHX and fat accumulation, fatty acid translocase (FAT/CD36), sterol regulatory element-binding protein (SREBP1c), peroxisome proliferator-activated receptor α (PPARα), proliferative cell nuclear antigen (PCNA) and ERα were examined by Oil Red O, qRT-PCR and immunohistochemistry, respectively. Hepatic fat accumulation was abundant in female and OVX-E compared to male and OVX rats. FAT/CD36 expression was observed in female, OVX and OVX-E at 0-12 hr after PHX, but not in male rats. At 0 hr, SREBP1c and PPARα were elevated in female and male rats, respectively, but were decreased after PHX in all rats. The PCNA labeling index reached a maximum at 36 hr and 48 hr in OVX-E and OVX rats, respectively. ERα expression in OVX-E was higher than OVX at 0-36 hr after PHX. In conclusion, these results indicated that estrogen and ERα might play an important role in fat accumulation related to FAT/CD36 during early phase of rat liver regeneration.
脂肪肝在男性和绝经后女性中很常见,这表明雌激素可能参与肝脏脂质代谢。本研究的目的是利用70%部分肝切除术(PHX)模型,明确雌激素和雌激素受体α(ERα)在雄性、雌性、去卵巢(OVX)和雌激素处理的去卵巢(OVX-E)大鼠肝脏再生过程中脂肪积累中的作用。在PHX后0-48小时采集肝脏组织,分别通过油红O、qRT-PCR和免疫组织化学检测脂肪积累、脂肪酸转运蛋白(FAT/CD36)、固醇调节元件结合蛋白(SREBP1c)、过氧化物酶体增殖物激活受体α(PPARα)、增殖细胞核抗原(PCNA)和ERα。与雄性和OVX大鼠相比,雌性和OVX-E大鼠肝脏脂肪积累丰富。PHX后0-12小时在雌性、OVX和OVX-E大鼠中观察到FAT/CD36表达,但在雄性大鼠中未观察到。在0小时时,雌性和雄性大鼠中SREBP1c和PPARα分别升高,但在所有大鼠PHX后均降低。PCNA标记指数在OVX-E和OVX大鼠中分别在36小时和48小时达到最大值。PHX后0-36小时,OVX-E中ERα表达高于OVX。总之,这些结果表明,雌激素和ERα可能在大鼠肝脏再生早期与FAT/CD36相关的脂肪积累中起重要作用。