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Background And Aims: Atherosclerosis is a chronic cardiovascular disease which is regarded as one of the most common causes of death in the elderly. Recent evidence has shown that atherosclerotic patients can benefit by targeting interleukin-1 beta (IL-1β). Aloperine (ALO) is an alkaloid which is mainly isolated from L.

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Aloperine Attenuates UVB-induced Damage in Skin Fibroblasts via Activating TFE3/Beclin-1-Mediated Autophagy.

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Background: Aloperine (ALO) is an important active ingredient in the traditional Chinese medicinal plant Sophora alopecuroides L and has a significant autophagy-stimulating effect. The effect of ALO on cytotoxicity caused by UVB radiation in skin fibroblasts and the potential mechanism remains unclear.

Objective: The present study aimed to assess the effect of ALO on UVB-induced damage in skin fibroblasts and investigate its possible mechanism.

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Article Synopsis
  • Aloperine (ALO) shows potential as a treatment for acute liver injury caused by acetaminophen (APAP) through its protective effects observed in animal models.
  • ALO administration before APAP exposure resulted in lower levels of damaging substances and reduced inflammation markers, indicating improved liver health.
  • The study suggests that ALO works by inhibiting specific signaling pathways and inflammatory responses linked to liver damage.
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Discovery of Aloperine as a Potential Antineoplastic Agent for Cholangiocarcinoma Harboring Mutant IDH1.

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Intrahepatic cholangiocarcinoma (ICC) is a universally lethal malignancy with increasing incidence. However, ICC patients receive limited benefits from current drugs; therefore, we must urgently explore new drugs for treating ICC. Quinolizidine alkaloids, as essential active ingredients extracted from , can suppress cancer cell growth via numerous mechanisms and have therapeutic effects on liver-related diseases.

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Aloperine protects the testis against testicular ischemia/reperfusion injury in rats.

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