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The two compounds have complementary tissue repair mechanisms

By inhibiting drug-metabolizing enzymes (e.g., cytochrome P450, UDP-glucuronosyltransferase) and enhancing intestinal absorption (21, 32), PPR significantly inhibits P-glycoprotein (P-gp) and enhances the efficacy of co-administered compounds like CUR and RSV, positioning it as a critical adjunct in nutraceutical formulations (33, 34)

2d, P 0.05) between two groups (Fig

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Stable gastric pentadecapeptide BPC 157 as useful cytoprotective therapy in the heart disturbances, myocardial infarction, heart failure, pulmonary hypertension, arrhythmias, and thrombosis presentation