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益生菌混合物(乳杆菌和双歧杆菌)通过 Gpr109a 和共生代谢产物丁酸缓解非酒精性脂肪性肝病大鼠的全身肥胖和炎症。

Probiotic mixture of Lactobacillus and Bifidobacterium alleviates systemic adiposity and inflammation in non-alcoholic fatty liver disease rats through Gpr109a and the commensal metabolite butyrate.

机构信息

School of Nursing, Jinan University, 601 Huangpu Road West, Guangzhou, 510632, Guangdong, China.

School of Basic Medicine, Jinan University, 601 Huangpu Road West, Guangzhou, 510632, Guangdong, China.

出版信息

Inflammopharmacology. 2018 Aug;26(4):1051-1055. doi: 10.1007/s10787-018-0479-8. Epub 2018 Apr 10.

Abstract

AIMS

The study explored the systemic adiposity and inflammation through Gpr109a and the commensal metabolite butyrate during the treatment of non-alcoholic fatty liver disease rats with the probiotic mixture of Lactobacillus and Bifidobacterium for 16 weeks.

METHODS

Fifteen male SD rats were randomly divided into three groups of five rats each: normal control group (basal feed), high-fat diet (HFD) feeding group (83% basal feed + 10% lard oil + 5% sucrose + 1.5% cholesterol + 0.5% cholate), and probiotic mixture intervention group (HFD + 0.6 g kg day probiotic mixture). Body composition, serum lipids, serum inflammatory markers, Gpr109a, and the commensal metabolite butyrate were assessed.

RESULTS

Compared with HFD group, probiotic mixture significantly reduced body weight and the levels of serum FFA, TG, ALT, IL-1β, and IL-18 (P < 0.05). The levels of Gpr109a and the commensal metabolite butyrate also changed significantly (P < 0.05).

CONCLUSIONS

Probiotic mixture might inhibit systemic adiposity and inflammation through Gpr109a and the commensal metabolite butyrate in response to the insult of HFD.

摘要

目的

本研究通过 Gpr109a 及共生代谢物丁酸盐,探讨了在 16 周的时间里,益生菌混合物(乳杆菌和双歧杆菌)对非酒精性脂肪肝病大鼠进行治疗时的全身肥胖和炎症情况。

方法

15 只雄性 SD 大鼠随机分为三组,每组 5 只:正常对照组(基础饲料)、高脂肪饮食(HFD)喂养组(83%基础饲料+10%猪油+5%蔗糖+1.5%胆固醇+0.5%胆酸钠)和益生菌混合物干预组(HFD+0.6 g/kg/d 益生菌混合物)。评估身体成分、血清脂质、血清炎症标志物、Gpr109a 和共生代谢物丁酸盐。

结果

与 HFD 组相比,益生菌混合物显著降低了体重和血清游离脂肪酸(FFA)、甘油三酯(TG)、丙氨酸氨基转移酶(ALT)、白细胞介素-1β(IL-1β)和白细胞介素-18(IL-18)的水平(P<0.05)。Gpr109a 和共生代谢物丁酸盐的水平也发生了显著变化(P<0.05)。

结论

益生菌混合物可能通过 Gpr109a 和共生代谢物丁酸盐抑制全身肥胖和炎症,从而应对 HFD 的损伤。

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