Alpha-Lipoic Acid Alleviates Isoflurane-Induced Cognitive Dysfunction in Juvenile Mice by Activating Peroxisome Proliferator Activated Receptor Gamma Coactivator -1 Alpha

IF 6.9 Q1 FOOD SCIENCE & TECHNOLOGY
Food frontiers Pub Date : 2025-05-19 DOI:10.1002/fft2.70032
Xingkai Zhao, Donglu Wang, Shuai Li, Xueting Zhang, Zhenlei Zhou
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Abstract

Millions of children undergo general anesthesia annually, yet preclinical studies suggest early life exposure to anesthetics may disrupt central nervous system development and impair cognition. Effective neuroprotective strategies remain limited. α-Lipoic acid (ALA), a dietary antioxidant found in red meat and carrots, has demonstrated therapeutic potential in diabetic neuropathy, but its role in anesthesia-induced neurotoxicity is unclear. This study integrates mechanistic and functional analyses to evaluate ALA's neuroprotective effects. Isoflurane-exposed neonatal mice exhibited hippocampal metabolic dysregulation, with altered lactate, pyruvate, and adenosine triphosphate (ATP) levels, leading to cognitive dysfunction. Mechanistically, isoflurane suppressed peroxisome proliferator activated receptor gamma coactivator -1 alpha (PGC-1α), a key regulator of mitochondrial metabolism in astrocytes. Using in vitro models and in vivo cyclization recombinase (Cre)-lentivirus (LV)-mediated PGC-1α overexpression, we identified a PGC-1α-dependent pathway regulating pyruvate dehydrogenase (PDH) and lactate dehydrogenase B (LDHB), restoring astrocytic bioenergetics. Functionally, ALA supplementation not only activated PGC-1α but also provided direct metabolic substrates for PDH, enhancing mitochondrial function and reversing cognitive deficits. High-performance liquid chromatography revealed reduced endogenous ALA levels in isoflurane-exposed hippocampi, whereas dietary ALA restored its physiological concentration. This dual mechanism—PGC-1α activation and metabolic substrate provision—supports ALA's role in both mechanistic restoration and functional recovery. These findings provide the first evidence that dietary ALA supplementation mitigates anesthesia-induced neurotoxicity via PGC-1α-mediated metabolic reprogramming, highlighting its potential as a perioperative dietary intervention to reduce neurodevelopmental risks in pediatric populations.

Abstract Image

硫辛酸通过激活过氧化物酶体增殖物激活受体γ辅助激活因子-1 α减轻异氟醚诱导的幼年小鼠认知功能障碍
每年有数以百万计的儿童接受全身麻醉,然而临床前研究表明,生命早期接触麻醉剂可能会破坏中枢神经系统的发育并损害认知能力。有效的神经保护策略仍然有限。α-硫辛酸(ALA)是一种在红肉和胡萝卜中发现的膳食抗氧化剂,已被证明在糖尿病神经病变中具有治疗潜力,但其在麻醉诱导的神经毒性中的作用尚不清楚。本研究结合机制和功能分析来评估ALA的神经保护作用。异氟醚暴露的新生小鼠表现出海马代谢失调,乳酸、丙酮酸和三磷酸腺苷(ATP)水平改变,导致认知功能障碍。机制上,异氟醚抑制过氧化物酶体增殖物激活受体γ辅助激活因子-1α (PGC-1α),这是星形胶质细胞线粒体代谢的关键调节因子。通过体外模型和体内环化重组酶(Cre)-慢病毒(LV)介导的PGC-1α过表达,我们发现PGC-1α依赖通路调节丙酮酸脱氢酶(PDH)和乳酸脱氢酶B (LDHB),恢复星形细胞的生物能量。在功能上,补充ALA不仅激活了PGC-1α,还为PDH提供了直接的代谢底物,增强了线粒体功能,逆转了认知缺陷。高效液相色谱法显示,暴露于异氟醚的海马内源性ALA水平降低,而膳食ALA恢复其生理浓度。这种双重机制- pgc -1α激活和代谢底物提供-支持ALA在机制恢复和功能恢复中的作用。这些发现提供了第一个证据,证明膳食补充ALA通过pgc -1α-介导的代谢重编程减轻了麻醉诱导的神经毒性,突出了其作为围手术期饮食干预降低儿科人群神经发育风险的潜力。
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来源期刊
CiteScore
10.50
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0.00%
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10 weeks
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