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  • 【IF8.3】褪黑素通過調節(jié)NADPH氧化酶4誘導的鐵細胞下垂和減輕線粒體功能障礙來緩解骨關節(jié)炎

【IF8.3】褪黑素通過調節(jié)NADPH氧化酶4誘導的鐵細胞下垂和減輕線粒體功能障礙來緩解骨關節(jié)炎

分類:引用文獻   發(fā)布時間 2024/9/10   閱讀: 572
期刊名稱:Journal of Pineal Research
影響因子:8.3
文章題目:Melatonin Alleviates Osteoarthritis by Regulating NADPH Oxidase 4–Induced Ferroptosis and Mitigating Mitochondrial Dysfunction
DOI: https://doi.org/10.1111/jpi.12992
第一作者:Qi Wang| Beijie Qi | Shi Shi | Weihao Jiang | Dejian Li | Xinhua Jiang | Chengqing Yi
作者單位:復旦大學浦東醫(yī)學中心上海浦東醫(yī)院
引用YOBIBIO產品:

U96-1494E  Mouse IL-1β ELISA Kit

U96-3112E  Mouse TNF-α ELISA kit


文章摘要:

Recent evidence indicates that the damaged regions in osteoarthritis are accompanied by the accumulation of iron ions. Ferroptosis, as an iron-dependent form of cell death, holds significant implications in osteoarthritis. Melatonin, a natural product with strong scavenging abilities against reactive oxygen species and lipid peroxidation, plays a crucial role in the treatment of osteoarthritis. This study aims to demonstrate the existence of ferroptosis in osteoarthritis and explore the specific mechanism of melatonin in suppressing ferroptosis and alleviating osteoarthritis. Our findings reveal that melatonin reverses inflammation-induced oxidative stress and lipid peroxidation while promoting the expression of extracellular matrix components in chondrocytes, safeguarding the cells. Our research has revealed that NADPH oxidase 4 (NOX4) serves as a crucial molecule in the ferroptosis process of osteoarthritis. Specifically, NOX4 is located on mitochondria in chondrocytes, which can induce disorders in mitochondrial energy metabolism and dysfunction, thereby intensifying oxidative stress and lipid peroxidation. LC-MS analysis further uncovered that GRP78 is a downstream binding protein of NOX4. NOX4 induces ferroptosis by weakening GRP78's protective effect on GPX4 and reducing its expression. Melatonin can inhibit the upregulation of NOX4 on mitochondria and mitigate mitochondrial dysfunction, effectively suppressing ferroptosis and alleviating osteoarthritis. This suggests that melatonin therapy represents a promising new approach for the treatment of osteoarthritis.

最近的證據(jù)表明,骨關節(jié)炎的損傷區(qū)域伴隨著鐵離子的積累。鐵下垂作為一種鐵依賴性細胞死亡形式,在骨關節(jié)炎中具有重要意義。褪黑素是一種天然產物,具有很強的清除活性氧和脂質過氧化的能力,在骨關節(jié)炎的治療中起著至關重要的作用。本研究旨在證明骨關節(jié)炎中鐵下垂的存在,并探討褪黑素抑制鐵下垂、緩解骨關節(jié)炎的具體機制。我們的研究結果表明,褪黑激素逆轉炎癥誘導的氧化應激和脂質過氧化,同時促進軟骨細胞中細胞外基質成分的表達,保護細胞。我們的研究發(fā)現(xiàn)NADPH氧化酶4 (NOX4)在骨關節(jié)炎的鐵下垂過程中起著至關重要的作用。具體來說,NOX4位于軟骨細胞的線粒體上,可誘導線粒體能量代謝紊亂和功能障礙,從而加劇氧化應激和脂質過氧化。LC-MS分析進一步發(fā)現(xiàn)GRP78是NOX4的下游結合蛋白。NOX4通過削弱GRP78對GPX4的保護作用并降低其表達而誘導鐵下垂。褪黑素可以抑制線粒體NOX4的上調,減輕線粒體功能障礙,有效抑制鐵下垂,緩解骨關節(jié)炎。這表明褪黑素治療代表了治療骨關節(jié)炎的一種有希望的新方法。

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