小鼠研究:中枢注射富血小板血浆可促进饮食诱导肥胖小鼠减重
Central platelet-rich plasma administration promotes weight loss in diet-induced obese mice
在饮食诱导肥胖(DIO)小鼠中,单次脑室内注射富血小板血浆(PRP)使体重下降,效果持续整个7天观察期。PRP还降低累积进食量、相对性腺白色脂肪重量和空腹血糖,并提高能量消耗、耗氧量、脂肪利用和活动量;弓状核小胶质细胞IBA1阳性面积减少而数量不变。该预印本尚未经同行评审,结果来自小鼠,不能外推到人类减重。
Aims: Platelet-rich plasma (PRP) contains diverse bioactive factors, but its potential role in central regulation of energy balance remains unexplored. This study investigated whether central PRP administration alters metabolic homeostasis in diet-induced obese (DIO) mice and examined associated hypothalamic responses under obese and inflammatory conditions. Materials and Methods: PRP was administered intracerebroventricularly in mouse models of DIO and lipopolysaccharide (LPS)-induced systemic inflammation. Body weight, food intake, energy metabolism, and adiposity were assessed alongside hypothalamic microglial morphology and transcriptomic profiling. Results: A single intracerebroventricular PRP injection reduced body weight in DIO mice, with the effect persisting throughout the 7-day observation period. PRP also decreased cumulative food intake, relative gonadal white adipose tissue weight, and fasting glucose, accompanied by increased energy expenditure, oxygen consumption, fat utilization, and physical activity. In both DIO and LPS-treated mice, PRP reduced IBA1-positive area per microglial cell in the arcuate nucleus without altering microglial number. Hypothalamic RNA sequencing revealed changes in immune and metabolic signaling, extracellular matrix organization, and growth-related pathways, suggesting a complex transcriptional response rather than uniform suppression of inflammation. Conclusions: A single central PRP administration induces sustained weight loss and favorable metabolic changes in DIO mice, accompanied by region-specific hypothalamic microglial and transcriptional responses. These findings identify central PRP as a potential modulator of energy balance and provide a basis for investigating its active components and underlying mechanisms.
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来源:bioRxiv · Neuroscience · biorxiv.org