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Research
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Post Treatment With
Silymarin Reduces The Degree Of Alpha-Naphthylisothiocyanate-Induced
Liver Injury.
Earl Benjamin III*,
C. Reese, T.V. Martin, Y.Hijji and D. Hill, School of Computer,
Mathematical and Natural Sciences, Department of Biology, Morgan
State University, MD, USA. Presented At The Morgan State University
9th Annual
Undergraduate & Graduate Science Research Symposium Program
(2002)
Previous
studies in our laboratory have demonstrated that pre-treatment with
Silymarin (polyphenolic flavonoid derived from milk thistle seeds)
is protective against the neutrophil-dependent hepatotoxicity of
alpha-naphthylisothiocyanate (ANIT) in rodents. This hepatotoxicity
is manifested as plasma elevations of hepato-specific enzymes,
hepato-cellular necrosis, and a pronounced influx of neutrophils.
Conversely, the effect of Silymarin post-treatment on ANIT-induced
liver injury requires further elucidation. Thus, the present study
was designed to test the hypothesis that post-treatment with
Silymarin reduces the degree of ANIT-induced liver injury. Male
Sprague Dawley rate received 120 mg/kg (oral) at either 0, 6, 12,
18, or 24 hours after ANIT administration. Twenty-four hours after
the administration of ANIT, plasma samples were collected, processed
and analyzed for markers of hepatic injury. Elevation in plasma
levels of aspartate aminotransferase (AST), alanine aminotransferase
(ALT), and gamma-glutamyltranspeptidase (GGT) were used as the
specific markers of ANIT-induced hepatotoxicity. Post-treatment with
50 mg/kg Silymarin afforded a modest degree of hepato-protection as
indicated by plasma elevations of AST, ALT, and GGT. These data
suggest that post-treatment with Silymarin affords a modest degree
of protection against the hepatotoxicity of ANIT. (Suppprted by NIH
Grant RR11606-5)
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