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The greater weight loss achieved with semaglutide may contribute to its enhanced hepatic benefits

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The drug is primarily metabolized through proteolytic degradation and does not undergo hepatic cytochrome P450 metabolism, which significantly reduces the potential for drug-drug interactions with medications metabolized through these pathways

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which found that Dula decreased TGF-1 level due to its anti-inflammatory effects on inflammatory signaling, oxidative stress, and cytokine production in obesity-induced airway hyperresponsiveness and fibrosis in a mouse model (Park et al

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