Hepatoprotective Phenylpropanoids from Scrophularia buergeriana Roots against CCl₄-Induced Toxicity: Action Mechanism and Structure-Activity Relationship

Abstract

Phenylpropanoids isolated from the roots of Scrophularia buergeriana MIQ. (Scrophulariaceae) protected primary cultures of rat hepatocytes from toxicity induced by carbon tetrachloride (CCl₄). In this report, we show that two of these phenylpropanoids, 4-O-E-p-methoxycinnamoyl-α-L-rhamnopyranoside ester (1) and p-methoxycinnamic acid (3) have significant hepatoprotective activity; another phenylpropanoid used for comparison, isoferulic acid (11), was equally active. To determine the mechanism(s) by which these three phenylpropanoids exerted their hepatoprotective activity, we measured activities of enzymes involved in the glutathione (GSH) redox system and assayed the level of hepatic mitochondrial GSH. The GSH levels in primary cultures of rat hepatocytes were significantly reduced with CCl₄ insult, but were significantly preserved by the treatment with these three phenylpropanoids. The activities of glutathione disulfide reductase and glutathione-S-transferase which normally decrease in CCl₄-injured rat hepatocytes were significantly preserved by the treatment with these three phenylpropanoids. In addition, in CCl₄-injured rat hepatocytes, the increased formation of malondialdehyde, a byproduct of lipid peroxidation, was reduced by the treatment with these phenylpropanoids. We determined the essential structural moiety within these three phenylpropanoids needed to exert hepatoprotective activity. The α,β-unsaturated ester moiety seemed to be essential for exerting hepatoprotective activity.

Abbreviations

CCl₄:carbon tetrachloride

GSH:glutathione

MDA:malondialdehyde

GST:glutathione-S-transferase

GPx:glutathione peroxidase

GR:glutathione disulfide reductase

Key words

Scrophularia buergeriana - Scrophulariaceae - phenylpropanoids - carbon tetrachloride - hepatoprotective activity - structure-activity relationship

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