TY - JOUR
T1 - Resolution of liver fibrosis in chronic CCl4 administration in the rat after discontinuation of treatment
T2 - Effect of silymarin, silibinin, colchicine and trimethylcolchicinic acid
AU - Muriel, Pablo
AU - Moreno, Mario G.
AU - Hernández, Maria Del C.
AU - Chávez, Enrique
AU - Alcantar, Lidia K.
PY - 2005/5
Y1 - 2005/5
N2 - The purpose of this work was to obtain a suitable model of fibrosis, in which spontaneous reversion was minimal, to study the ability of silymarin, silibinin, colchicine and trimethylcolchicinic acid (TMCA) to reverse it. Reversal of liver fibrosis was studied in male Wistar rats after one, two or three months of CCl4 administration (0.4 g/kg intraperitoneally, three times per week), by discontinuation of the toxin for 2 months. Silymarin (50 mg/kg), silibinin (50 mg/kg), colchicine (10 μg/rat) and trimethylcolchicinic acid (100 μg/rat) were administered daily, by gavage, after 3 months of CCl4 administration. Collagen content was determined by measuring hydroxyproline in liver samples; glycogen, was determined utilizing the anthrone reagent; Mallory's trichromic stains of liver sections were performed. The best scheme of treatment was obtained when CCl 4 was administered during three months (collagen increased 6 times). Discontinuation of the toxin for two months produced a significant but relative small reduction of fibrosis (collagen was still 4.5 times over control). Colchicine, TMCA, silymarin or silibinin treatment showed no significant fibrolitic effect. This scheme of treatment may be an excellent tool to study the ability of drugs to reverse fibrosis. The hepatoprotective properties of silymarin, silibinin, colchicine and trimethylcolchinic acid may be irrelevant to reverse established cirrhosis.
AB - The purpose of this work was to obtain a suitable model of fibrosis, in which spontaneous reversion was minimal, to study the ability of silymarin, silibinin, colchicine and trimethylcolchicinic acid (TMCA) to reverse it. Reversal of liver fibrosis was studied in male Wistar rats after one, two or three months of CCl4 administration (0.4 g/kg intraperitoneally, three times per week), by discontinuation of the toxin for 2 months. Silymarin (50 mg/kg), silibinin (50 mg/kg), colchicine (10 μg/rat) and trimethylcolchicinic acid (100 μg/rat) were administered daily, by gavage, after 3 months of CCl4 administration. Collagen content was determined by measuring hydroxyproline in liver samples; glycogen, was determined utilizing the anthrone reagent; Mallory's trichromic stains of liver sections were performed. The best scheme of treatment was obtained when CCl 4 was administered during three months (collagen increased 6 times). Discontinuation of the toxin for two months produced a significant but relative small reduction of fibrosis (collagen was still 4.5 times over control). Colchicine, TMCA, silymarin or silibinin treatment showed no significant fibrolitic effect. This scheme of treatment may be an excellent tool to study the ability of drugs to reverse fibrosis. The hepatoprotective properties of silymarin, silibinin, colchicine and trimethylcolchinic acid may be irrelevant to reverse established cirrhosis.
UR - http://www.scopus.com/inward/record.url?scp=18744393745&partnerID=8YFLogxK
U2 - 10.1111/j.1742-7843.2005.pto_06.x
DO - 10.1111/j.1742-7843.2005.pto_06.x
M3 - Artículo
SN - 1742-7835
VL - 96
SP - 375
EP - 380
JO - Basic and Clinical Pharmacology and Toxicology
JF - Basic and Clinical Pharmacology and Toxicology
IS - 5
ER -