Shi Xueying, Guo Qingqing, Li Xiangce, Li Tongqing, Li Tao, Li Tianyu, Zhang Peiyu, Li Zhi, Liu Haiyan
Hebei Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, College of Life Sciences, Hebei Normal University, Shijiazhuang 050024, China.
Hebei Fisheries Technology Extension Center, Shijiazhuang 050051, China.
Comp Biochem Physiol Part D Genomics Proteomics. 2025 Mar 18;55:101486. doi: 10.1016/j.cbd.2025.101486.
Animals frequently suffer from starvation throughout their life cycle; however, the mobilization and utilization of energy sources can differ. To clarify the fundamental mechanisms underlying energy mobilization and metabolic adjustment in response to food deprivation in the soft-shelled turtle (Pelodiscus sinensis), eighty turtles (initial body weight, 51.81 ± 0.29 g) were subjected to starvation periods of 1 d, 4 d, 8 d, 16 d, and 32 d (referred to as S1, S4, S8, S16, and S32). The results showed that the greatest absolute loss in body composition occurred in moisture, followed by protein and lipid, respectively. Hepatic glycogen contents significantly decreased after 4 days of starvation and then remained stable. Notably, plasma glucose, cholesterol, and free fatty acid contents exhibited significant decreases from S8, while plasma triacylglycerol levels dramatically declined from S4. Gluconeogenesis-related genes (pepck, g6pase) were upregulated in the starving turtles to maintain glucose homeostasis. Comparative analyses between S32 and S1 groups identified a total of 6051 differential genes and 150 differential metabolites, highlighting three overlapping metabolic pathways: glycerophospholipid metabolism, alanine, aspartate, and glutamate metabolism, and taurine and hypotaurine metabolism. Integrative analyses further revealed increased levels of specific metabolites, including phosphatidylcholine, phosphatidylethanolamine, glycerophosphocholine, L-2-aminoethyl seryl phosphate, l-serine-phosphatidylethanolamine, adenyiosuccinate, 5-phosphoribosylamine, and taurine. These metabolites are vital for amino acid-driven gluconeogenesis, cell membrane stability, and mitigating cellular damage resulting from food deprivation. In conclusion, glucose homeostasis was maintained by enhancing gluconeogenesis in P. sinensis during extended periods of starvation, and the activation of lipid and amino acid metabolism represents an adaptive metabolic strategy employed by P. sinensis to cope with starvation conditions.
动物在其生命周期中经常遭受饥饿;然而,能量来源的动员和利用可能有所不同。为了阐明中华鳖应对食物剥夺时能量动员和代谢调节的基本机制,将80只鳖(初始体重51.81±0.29克)分别进行1天、4天、8天、16天和32天的饥饿处理(分别称为S1、S4、S8、S16和S32)。结果表明,身体成分中绝对损失最大的是水分,其次是蛋白质和脂质。饥饿4天后肝糖原含量显著下降,然后保持稳定。值得注意的是,从S8开始,血浆葡萄糖、胆固醇和游离脂肪酸含量显著下降,而血浆三酰甘油水平从S4开始急剧下降。饥饿鳖体内糖异生相关基因(pepck、g6pase)上调以维持葡萄糖稳态。S32组和S1组之间的比较分析共鉴定出6051个差异基因和150种差异代谢物,突出了三个重叠的代谢途径:甘油磷脂代谢、丙氨酸、天冬氨酸和谷氨酸代谢以及牛磺酸和亚牛磺酸代谢。综合分析进一步揭示了特定代谢物水平的增加,包括磷脂酰胆碱、磷脂酰乙醇胺、甘油磷酸胆碱、L-2-氨基乙基丝氨酸磷酸、L-丝氨酸-磷脂酰乙醇胺、腺苷琥珀酸、5-磷酸核糖胺和牛磺酸。这些代谢物对于氨基酸驱动的糖异生、细胞膜稳定性以及减轻食物剥夺导致的细胞损伤至关重要。总之,在长期饥饿期间,中华鳖通过增强糖异生来维持葡萄糖稳态,脂质和氨基酸代谢的激活代表了中华鳖应对饥饿条件所采用的一种适应性代谢策略。