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Recent advances in plant hepatoprotectives - CIMAP Staff - Central ...

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RECENT ADVANCES IN PLANT HEPATOPROTECTIVES<br />

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751<br />

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Figure 3. Structures of andrographolide (4), neoandrographolide (5), andrographoside (6), and andrograpan<strong>in</strong> (7).<br />

natalensis. 53 Andrographolide has shown choleretic activity <strong>in</strong> the rats and gu<strong>in</strong>ea pigs, stimulat<strong>in</strong>g<br />

bile production. 54<br />

Andrographolides are distributed throughout the viscera when consumed orally and 90% is<br />

excreted with<strong>in</strong> 48 hr of consumption. Four ma<strong>in</strong> metabolites (Fig. 4) of andrographolide as<br />

sulphonates (M-1, M-2, M-3, and M-4) were isolated from rat ur<strong>in</strong>e and feces after 48 hr of oral<br />

adm<strong>in</strong>istration at room temperature. 55<br />

D. Mode of Action<br />

Andrographolide, andrographoside, and neoandrographolide protect liver aga<strong>in</strong>st the hepatotox<strong>in</strong>s<br />

by reduc<strong>in</strong>g the levels of the lipid oxidation product, malondialdehyde (MDA), and by ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g<br />

high levels of the reduced form of glutathione (GSH). 56 The lower<strong>in</strong>g of MDA formation revealed the<br />

free radical scaveng<strong>in</strong>g properties of diterpene lactones. On the other hand, neoandrographolide has<br />

12<br />

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M-2, 12S<br />

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M-3 M-4<br />

Medic<strong>in</strong>al Research Reviews DOI 10.1002/med<br />

Figure 4. Metabolites of andrographolide.

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