Hegde Pramukh Subrahmanya, Agni Megha Bhat, Rai Praveen, Sadananda Monika, Mirajkar A M, Kumar B Mohana, Ranade Anu V, Gowda K M Damodara
Department of Physiology, K S Hegde Medical Academy, Nitte (Deemed to Be University), Karnataka, Deralakatte, Mangalore, 575018, India.
Department of Infectious Diseases and Microbial Genomics, Nitte University Centre for Science Education and Research (NUCSER), Nitte (Deemed to Be University), Deralakatte, Mangalore, 575018, India.
Learn Behav. 2025 May 8. doi: 10.3758/s13420-025-00673-4.
Perinatal undernutrition sensitizes offspring to the development of chronic adult metabolic diseases, including cognitive dysfunction, which poses significant public health issues. Undernutrition is the most powerful condition of physiological stress, and epidemiological studies indicate detrimental effects on cognitive function and behavior in human offspring exposed to inadequate perinatal nutrition, leading to increased peroxidation of PUFAs in the brain. To address these issues, the present study investigated the protective effects of the antioxidant nutraceuticals astaxanthin (AsX) and docosahexaenoic acid (DHA) on the protective effect of DHA in the presence of antioxidants on the cognitive dysfunction and oxidative stress induced by perinatal undernutrition. Using a Wistar rat model, AsX and DHA improved learning and memory skills in perinatally undernourished offspring. The cognitive parameters included the RAM and NOR tests, and the oxidative stress parameters were assessed by the estimation of GSH, MDA, total nitrite, and TAC. This study revealed spatial learning, memory dysfunction, and abnormal exploratory behavior in offspring exposed to perinatal undernutrition at different time points in postnatal life, and these effects were ameliorated by AsX and DHA. Similarly, oxidative stress induced by perinatal undernutrition was also ameliorated by AsX and DHA. Induced oxidative stress was significantly correlated with cognitive function. This study revealed the potential of AsX and DHA supplementation during the perinatal period for the future development of cognitive dysfunction.
围产期营养不良会使后代更容易患慢性成人代谢疾病,包括认知功能障碍,这带来了重大的公共卫生问题。营养不良是最严重的生理应激状况,流行病学研究表明,围产期营养不足会对人类后代的认知功能和行为产生有害影响,导致大脑中多不饱和脂肪酸(PUFA)过氧化增加。为了解决这些问题,本研究调查了抗氧化营养保健品虾青素(AsX)和二十二碳六烯酸(DHA)在存在抗氧化剂的情况下对围产期营养不良诱导的认知功能障碍和氧化应激的保护作用。使用Wistar大鼠模型,AsX和DHA改善了围产期营养不良后代的学习和记忆能力。认知参数包括放射状迷宫(RAM)和新奇事物识别(NOR)测试,氧化应激参数通过谷胱甘肽(GSH)、丙二醛(MDA)、总亚硝酸盐和总抗氧化能力(TAC)的测定来评估。本研究揭示了在出生后不同时间点暴露于围产期营养不良的后代存在空间学习、记忆功能障碍和异常探索行为,而AsX和DHA改善了这些影响。同样,围产期营养不良诱导的氧化应激也被AsX和DHA改善。诱导的氧化应激与认知功能显著相关。本研究揭示了围产期补充AsX和DHA对未来认知功能障碍发展的潜在作用。