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학술논문

Shikonin attenuates blood–brain barrier injury and oxidative stress in rats with subarachnoid hemorrhage by activating Sirt1/Nrf2/HO-1 signaling

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영문명
발행기관
대한생리학회-대한약리학회
저자명
Guanghu Li Yang'e Yi Sheng Qian Xianping Xu Hao Min Jianpeng Wang Pan Guo Tingting Yu Zhiqiang Zhang
간행물 정보
『The Korean Journal of Physiology & Pharmacology』제29권 제3호, 283~291쪽, 전체 9쪽
주제분류
의약학 > 의학일반
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발행일자
2025.05.01
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국문 초록

Subarachnoid hemorrhage (SAH) is a serious intracranial hemorrhage characterized by acute bleeding into the subarachnoid space. The effects of shikonin, a natural compound from the roots of Lithospermum erythrorhizon, on oxidative stress and blood–brain barrier (BBB) injury in SAH was evaluated in this study. A rat model of SAH was established by endovascular perforation to mimic the rupture of intracranial aneurysms. Rats were then administered 25 mg/kg of shikonin or dimethylsulfoxide after surgery. Brain edema, SAH grade, and neurobehavioral scores were measured after 24 h of SAH to evaluate neurological impairment. Concentrations of the oxidative stress markers superoxide dismutase (SOD), glutathione (GSH), and malondialdehyde (MDA) in the brain cortex were determined using the corresponding commercially available assay kits. Evans blue staining was used to determine BBB permeability. Western blotting was used to quantify protein levels of tight junction proteins zonula occludens-1, Occludin, and Claudin-5. After modeling, the brain water content increased significantly whereas the neurobehavioral scores of rats with SAH decreased prominently. MDA levels increased and the levels of the antioxidant enzymes GSH and SOD decreased after SAH. These changes were reversed after shikonin administration. Shikonin treatment also inhibited Evans blue extravasation after SAH. Furthermore, reduction in the levels of tight junction proteins after SAH modeling was rescued after shikonin treatment. In conclusion, shikonin exerts a neuroprotective effect after SAH by mitigating BBB injury and inhibiting oxidative stress in the cerebral cortex.

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APA

Guanghu Li,Yang'e Yi,Sheng Qian,Xianping Xu,Hao Min,Jianpeng Wang,Pan Guo,Tingting Yu,Zhiqiang Zhang. (2025).Shikonin attenuates blood–brain barrier injury and oxidative stress in rats with subarachnoid hemorrhage by activating Sirt1/Nrf2/HO-1 signaling. The Korean Journal of Physiology & Pharmacology, 29 (3), 283-291

MLA

Guanghu Li,Yang'e Yi,Sheng Qian,Xianping Xu,Hao Min,Jianpeng Wang,Pan Guo,Tingting Yu,Zhiqiang Zhang. "Shikonin attenuates blood–brain barrier injury and oxidative stress in rats with subarachnoid hemorrhage by activating Sirt1/Nrf2/HO-1 signaling." The Korean Journal of Physiology & Pharmacology, 29.3(2025): 283-291

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