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The hepatoprotective task of CPP at 0, 10, 30, 50 mg per kg BW had been demonstrated in vivo by using ICR male mice provided with 40% v/v alcohol (5 ml per kg weight) everyday to induce alcohol liver injury. CPP could considerably improve the liquor metabolism in liver as evidenced by the improved activity of aspartate aminotransferase (AST) and alanine aminotransferase (ALT). The overexpression of serum tumefaction necrosis factor-α (TNF-α) and interleukin-β (IL
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