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柚皮苷可减轻氟诱导的神经损伤:聚焦于线粒体通透性转换孔介导的能量代谢调节。

Naringin alleviates fluoride-induced neurological impairment: A focus on the regulation of energy metabolism mediated by mitochondrial permeability transition pore.

机构信息

Department of Environmental Health & Environment and Health Innovation Team, School of Public Health, Zhengzhou University, Zhengzhou, Henan 450001, China; School of Water Conservancy Science and Engineering, Zhengzhou University, Zhengzhou, Henan 450001, China.

Department of Environmental Health & Environment and Health Innovation Team, School of Public Health, Zhengzhou University, Zhengzhou, Henan 450001, China.

出版信息

Sci Total Environ. 2024 Dec 10;955:177073. doi: 10.1016/j.scitotenv.2024.177073. Epub 2024 Oct 22.

Abstract

The neurological impairment induced by fluoride is associated with mitochondrial dysfunction. Normal mitochondrial permeability transition pore (mPTP) opening plays a pivotal role in mitochondrial function. However, it remains unclear whether p53-dependent mPTP-related mitochondrial apoptosis is associated with fluoride-induced neurological impairment, and the alleviation of naringin on those. In vivo, NaF-treated rats had impaired learning and memory abilities, damaged hippocampal structure, and higher respiratory exchange rates (RER). In vitro, the increased apoptosis rates, excessive opening of mPTP, and decreased mitochondrial membrane potential (MMP) were observed in PC12 cells treated with NaF. The protein expressions of p53, CytoC, and cleaved caspase 3 were significantly increased in hippocampi of rats treated with 50 mg/L and 100 mg/L NaF and in 40 mg/L and 80 mg/L NaF-treated PC12 cells, while the protein expression of CypD remains stable. And the changes of p53 and CypD were also confirmed by the immunofluorescence staining in vivo. After inhibiting the expression of p53 with pifithrin-α and p53-siRNA, the decreased apoptosis rates and mPTP opening, increased MMP, and decreased protein expressions of p53, CytoC, and cleaved caspase 3 were observed in NaF-treated PC12 cells. Rats, treated with NaF and naringin, had alleviated impaired neurological function, and had lower RER than rats treated with NaF alone. And compared with those in the NaF group, the decreased apoptosis rates and mPTP opening, and increased MMP were also found in PC12 cells treated with NaF and naringin. Furthermore, hippocampi of rats and PC12 cells treated with NaF and naringin had decreased protein expressions of p53, CytoC, and cleaved caspase 3. Our results indicate that fluoride activates the p53-dependent mPTP-related mitochondrial apoptosis, which then affects energy metabolism, resulting in neurological impairment. Additionally, naringin can alleviate this damage, and further studies on the potential health benefits of naringin are needed.

摘要

氟化物引起的神经损伤与线粒体功能障碍有关。正常的线粒体通透性转换孔(mPTP)开放对于线粒体功能至关重要。然而,p53 依赖性 mPTP 相关线粒体凋亡是否与氟化物诱导的神经损伤有关,以及柚皮苷对其的缓解作用仍不清楚。在体内,NaF 处理的大鼠表现出学习和记忆能力受损、海马结构损伤以及呼吸交换率(RER)升高。在体外,NaF 处理的 PC12 细胞中观察到凋亡率增加、mPTP 过度开放和线粒体膜电位(MMP)降低。用 50mg/L 和 100mg/L NaF 处理的大鼠海马和用 40mg/L 和 80mg/L NaF 处理的 PC12 细胞中,p53、CytoC 和 cleaved caspase 3 的蛋白表达显著增加,而 CypD 的蛋白表达保持稳定。体内免疫荧光染色也证实了 p53 和 CypD 的变化。用 pifithrin-α和 p53-siRNA 抑制 p53 的表达后,NaF 处理的 PC12 细胞中凋亡率降低、mPTP 开放减少、MMP 增加、p53、CytoC 和 cleaved caspase 3 的蛋白表达减少。与单独用 NaF 处理的大鼠相比,用 NaF 和柚皮苷处理的大鼠神经功能障碍得到缓解,RER 降低。与 NaF 组相比,NaF 和柚皮苷处理的 PC12 细胞中凋亡率降低、mPTP 开放减少、MMP 增加。此外,用 NaF 和柚皮苷处理的大鼠海马和 PC12 细胞中 p53、CytoC 和 cleaved caspase 3 的蛋白表达减少。我们的结果表明,氟化物激活了 p53 依赖性 mPTP 相关线粒体凋亡,进而影响能量代谢,导致神经损伤。此外,柚皮苷可以减轻这种损伤,需要进一步研究柚皮苷的潜在健康益处。

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