Abstract:
:Hepatic fibrosis is an outcome of chronic liver injury. Angiotensin II (ANG II) may play a role in the pathogenesis of hepatic fibrosis. Certain drugs such as ACE inhibitors, ANG II antagonists, and even statins could interfere with the renin angiotensin system and modulate its deleterious effects. This study was carried out to investigate the possible role of losartan and atorvastatin in liver fibrosis. Liver fibrosis was induced in rats by i.p. injection of 50% CCl4 twice per week for 8 weeks. The rats intoxicated with CCl4 were divided into four groups: fibrosis control; losartan group; atorvastatin group; and co-treated group. A fifth group of normal healthy rats served as a control group. The results showed that losartan and atorvastatin, either alone or in combination, significantly decreased ALT, AST, hyaluronic acid and hydroxyproline levels in their groups compared to those of the fibrosis control group. A significant decrease in TGF-β was found in the losartan and co-treated groups but not in the atorvastatin group. These biochemical data were supported by liver histopathology and α-SMA. The results indicate that the combined treatment with both losartan and atorvastatin produced a greater effect than either drug alone and proved a beneficial role in inhibiting or reversing liver fibrosis.
journal_name
Clin Exp Pharmacol Physioljournal_title
Clinical and experimental pharmacology & physiologyauthors
El-Ashmawy NE,El-Bahrawy HA,Shamloula MM,Ibrahim AOdoi
10.1111/1440-1681.12446subject
Has Abstractpub_date
2015-09-01 00:00:00pages
979-987issue
9eissn
0305-1870issn
1440-1681journal_volume
42pub_type
杂志文章abstract::1. The role of the arterial and cardiac baroreceptors on the arginine vasopressin (AVP) and plasma renin activity (PRA) responses to haemorrhage was studied in conscious rabbits. They were bled at a rate of approximately 3% of their blood volume (BV)/min, both when the autonomic nervous system (ANS) was intact and dur...
journal_title:Clinical and experimental pharmacology & physiology
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doi:10.1111/j.1440-1681.1992.tb00412.x
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1111/j.1440-1681.1978.tb00674.x
更新日期:1978-05-01 00:00:00
abstract::1. Chromium picolinate (CrPic) has been recommended as an alternative therapeutic regimen for Type 2 diabetes mellitus (T2DM). However, the molecular mechanism underlying the action of CrPic is poorly understood. 2. Using normal and insulin-resistant 3T3-L1 adipocytes, we examined the effects of CrPic on the gene tran...
journal_title:Clinical and experimental pharmacology & physiology
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更新日期:2009-08-01 00:00:00
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pub_type: 杂志文章,评审
doi:10.1111/j.1440-1681.2009.05331.x
更新日期:2010-04-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章,评审
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pub_type: 杂志文章
doi:10.1111/j.1440-1681.1975.tb01828.x
更新日期:1975-03-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1111/j.1440-1681.1980.tb00084.x
更新日期:1980-07-01 00:00:00
abstract::1. Stretch-induced muscle injury results in the damage that causes reduced force and increased membrane permeability. This muscle damage is caused, in part, by ionic entry through stretch-activated channels and blocking these channels with Gd3+ or streptomycin reduces the force deficit associated with damage. 2. Dystr...
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pub_type:
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更新日期:2004-08-01 00:00:00
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pub_type: 杂志文章,评审
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更新日期:1997-08-01 00:00:00
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pub_type: 杂志文章
doi:10.1111/j.1440-1681.1977.tb02683.x
更新日期:1977-11-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1111/j.1440-1681.1976.tb00633.x
更新日期:1976-11-01 00:00:00
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pub_type: 杂志文章
doi:10.1046/j.1440-1681.1999.03161.x
更新日期:1999-11-01 00:00:00
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pub_type: 杂志文章
doi:10.1111/j.1440-1681.1994.tb02515.x
更新日期:1994-04-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1111/j.1440-1681.2007.04583.x
更新日期:2007-05-01 00:00:00
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pub_type: 杂志文章
doi:10.1111/1440-1681.13402
更新日期:2020-09-05 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
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pub_type: 杂志文章
doi:10.1111/j.1440-1681.1996.tb01169.x
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更新日期:2005-05-01 00:00:00
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pub_type: 杂志文章
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更新日期:2006-11-01 00:00:00
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doi:10.1111/1440-1681.12378
更新日期:2015-05-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1111/j.1440-1681.1988.tb01075.x
更新日期:1988-04-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1111/j.1440-1681.1980.tb00062.x
更新日期:1980-03-01 00:00:00
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doi:10.1111/1440-1681.12408
更新日期:2015-06-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
pub_type: 杂志文章
doi:10.1046/j.1440-1681.2002.03748.x
更新日期:2002-10-01 00:00:00
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pub_type: 杂志文章
doi:10.1046/j.1440-1681.2001.03527.x
更新日期:2001-10-01 00:00:00
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journal_title:Clinical and experimental pharmacology & physiology
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doi:10.1111/j.1440-1681.1991.tb01375.x
更新日期:1991-01-01 00:00:00
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pub_type: 杂志文章
doi:10.1111/j.1440-1681.1986.tb00337.x
更新日期:1986-03-01 00:00:00