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C. cochlearium 2316 Ameliorates High-Fat Diet-Induced Obesity and Metabolic Syndrome Risk Factors via Enhanced Energy Expenditure and Glucose Homeostasis.

Wenjun Zhu, Paba Edirisuriya, Qing Ai, Fei Yang et al.

Kernaussage

Supplementation with Clostridium cochlearium 2316 significantly mitigated high-fat diet-induced obesity and metabolic dysfunction by reducing body weight gain by 17.3%, improving glucose homeostasis (89.4% HOMA-IR reduction), and increasing basal metabolic rate and energy expenditure.

Abstract

This study investigated the potential beneficial effects of a probiotic candidate, Clostridium cochlearium 2316, in modulating physiological and metabolic markers in mice with high-fat diet-induced obesity (DIO). C57BL/6 DIO mice were assigned to three groups (ad libitum): standard low-fat control (LF, 10% fat), high-fat diet (HF, 60% fat), and high-fat diet supplemented with approximately one billion CFU/day of CC2316 via daily oral gavage for 16 weeks. After 16 weeks, the CC group exhibited 17.3% lower body weight gain ( p < 0.001) and significant fat mass decrease ( p < 0.0001) compared to HF mice. Serum biochemistry showed that CC2316 supplementation resulted in a 27.7% reduction in fasting blood glucose ( p < 0.05), a 58.4% reduction in fasting insulin ( p < 0.01), and an 89.4% improvement in HOMA-IR score ( p < 0.05). Furthermore, serum total cholesterol level decreased dramatically by 40.2% in the CC group ( p < 0.001). Despite a higher caloric absorption rate ( p < 0.001), CC mice demonstrated a significant beneficial shift in energy expenditure, characterized by an increased basal metabolic rate ( p < 0.05), higher energy expenditure ( p < 0.05), and an elevated respiratory quotient (RER) ( p < 0.05), alongside increased physical activity ( p < 0.05). This investigation strongly suggests that CC2316 supplementation mitigates the adverse effects of HFD-induced obesity by modulating whole-body energy metabolism, positioning it as a potential aid to lower risk factors associated with metabolic syndrome. The precise mechanisms linking the gut microbiome to altered energy substrate utilization are discussed and suggested for further investigation.

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Quelle: PubMed Central / National Library of Medicine (NLM). Apollion steht in keiner Verbindung mit NLM und wird von NLM nicht empfohlen. Evidenzgrade bewerten die methodische Studienqualität — nicht die inhaltliche Richtigkeit.

Lizenz: CC BY — Inhalte werden ausschließlich aus Open-Access-Quellen mit kommerziell nutzbaren Lizenzen (CC0, CC BY, CC BY-SA) indexiert.