JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES) ›› 2009, Vol. 47 ›› Issue (12): 38-41.
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WANG Na, QI Min, LIANG Suren, FENG Jinbo, PENG Tao, PEI Fei, HU Zhao
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Abstract:
To explore the mechanisms of the beneficial effects of Niaoduqing, and to investigate the effects of Niaoduqing on expressions of renal transforming growth factorbetal, and tissue inhibition of metalloproteinase1, plasminogen activator inhibitor1 and osteopontin mRNAs in rats with Adriamycininduced nephropathy. MethodsThe male rats were randomly divided into four groups: the normal group(N group), the model group(M group), the Niaoduqing group(Ni group)and the Benazepril group(B group). 24hour urinary protein excretion and renal function were determined at 4 and 8 weeks. Expressions of transforming growth factorbetal(TGFβ1), tissue inhibition of metalloproteinase1( TIMP1), plasminogen activetor inhibitor1(PAI1) and osteopontin (OPN) mRNA were determined by realtime quantitative RTPCR. ResultsNiaoduqing and Benazepril effectively reduced the levels of 24hour urinary protein excretion, Bun, and Scr, elevated protein levels, corrected fat metabolic disorder, and downregulated expressions of TGFβ1, TIMP1, PAI1 and OPN mRNAs(P<0.01)compared with the M group. Niaoduqing could significantly inhibit expression of PAI1 mRNA compared with that of Benazepril(P<0.01). ConclusionNiaoduqing can downregulate expressions of TGFβ1, TIMP1, PAI1 and OPN mRNAs in renal tissues of rats with Adriamycininduced nephropathy, which may be its active mechanism in treating chronic renal diseases.
Key words: Niaoduqing; Adriamycin nephropathy; Transforming growth factorbetal; Tissue inhibition of metalloproteinase1; Plasminogen activatorinhibitor1; Osteopontin; Rats; Model, animal
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https://yxbwk.njournal.sdu.edu.cn/EN/Y2009/V47/I12/38
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