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Inhibitory effect of angiotensin II receptor antagonist on hepatic stellate cell activation in non-alcoholic steatohepatitis
被引:86
|作者:
Yokohama, Shiro
Tokusashi, Yoshihiko
Nakamura, Kimihide
Tamaki, Yosui
Okamoto, Satoshi
Okada, Mituyoshi
Aso, Kazunobu
Hasegawa, Takenao
Aoshima, Masaru
Miyokawa, Naoyuki
Haneda, Masakazu
Yoneda, Masashi
机构:
[1] Asahikawa Med Coll, Dept Med 2, Asahikawa, Hokkaido 0788510, Japan
[2] Asahikawa Med Coll, Dept Surg Pathol, Asahikawa, Hokkaido 0788510, Japan
[3] Dokkyo Univ, Sch Med, Dept Gastroenterol, Mibu, Tochigi 32102, Japan
[4] Obihiro Univ Agr & Vet Med, Hlth Care Adm Ctr, Obihiro, Hokkaido 080, Japan
关键词:
NASH;
NAFLD;
hepatic fibrosis;
HSC;
losartan;
D O I:
10.3748/wjg.v12.i2.322
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
AIM: To investigate the efficacy of angiotensin II receptor antagonist on hepatic stellate cells (HSCs) activation in the patients with non-alcoholic steatohepatitis (NASH). METHODS: Seven patients with NASH were prescribed losartan, a selective angiotensin II type I receptor antagonist (50 mg/d) for 48 wk. Liver biopsies were performed both at the entry and end of the study in all patients. Quiescent and activated HSCs were identified by double immunostaining using anti-p75 and alpha-smooth muscle actin antibodies, and the number of each phenotype was counted. Similarly, the liver specimens obtained from the eight patients with non-alcoholic fatty liver (NAFL) were also examined as controls. RESULTS: In NASH hepatic tissues, activated HSCs were dominantly distributed as compared with those in NAFL. The 48-wk losartan treatment induced a remarkable decrease in activated HSCs,and a mild increase in quiescent phenotypes. CONCLUSION: Our data suggest the crucial involvement of HSCs in anti-fibrotic effect of angiotensin II receptor antagonist on patients with NASH. (c) 2006 The WIG Press. All rights reserved.
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页码:322 / 326
页数:5
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