Faculty of Pharmacy, Department of Biochemistry, Misr International University, Cairo, Egypt.
Faculty of Medicine for Girls (Cairo), Department of Physiology, Al-Azhar University, Cairo, Egypt.
J Cell Physiol. 2018 Jun;233(6):5044-5057. doi: 10.1002/jcp.26370. Epub 2018 Jan 5.
The recent appreciation of the energy burning capacity of brown adipose tissue turns it to an attractive target for anti-obesity therapy. We sought to evaluate the effect of L-carnosine on browning of white adipose tissue in exercised obese rats. Sixty adult male Wistar albino rats, 7-8 week-old weighing 130-150 g, were allocated into six groups; with 10 rats in each, for an experimentation period of 12 weeks: (i) normal control rats fed a standard fat diet (SFD/control), (ii) normal control rats fed a standard diet and injected with L-carnosine (250 mg/kg, i.p,) for 6 weeks (SFD/CAR), (iii) high-fat diet (HFD)-induced obese rats for 12 weeks, (iv) HFD rats subjected to exercise training (HFD/EXE) for 6 weeks, (v) HFD rats injected with L-carnosine (250 mg/kg,i.p.) for 6 weeks (HFD/CAR) and, (vi) HFD rats subjected to exercise training and L-carnosine (HFD/EXE/CAR). At the end of the 12-week-experiment, the body weights and the serum levels of lipid profile, oxidative stress, and inflammatory markers as well as circulating myokines were investigated. Gastrocnemius muscles and inguinal adipose tissues were excised for the measurement of gene expression of muscle irisin, adipose tissue uncoupling protein1 (UCP1), CD137 and the protein level of p38MAPK. In addition, histopathological examination for the studied groups was performed. Both exercise training for 6 weeks and carnosine treatment significantly decreased body weight gain, ameliorated obesity-induced dyslipidemia, reduced the thiobarbituric acid reactive species (TBARS) and TNF-α, while increased total antioxidant capacity and IL-10. Furthermore, increases in serum irisin levels and the expression of adipose uncoupling protein-1 (UCP-1), adipose CD137, p38 MAPK, and muscular fibronectin type III domain-containing protein 5(FNDC5), the precursor of irisin gene expression, were correlated with these carnosine- and exercise-induced physiological improvements. The highest improvement was evident in the combined exercise and carnosine group which indicates that their beneficial effects in obese animals were synergistic. These findings suggest that L-carnosine may induce browning of adipose tissue through irisin stimulation, a phenomenon that could be related to its antioxidant, anti-inflammatory, and anti-obesity effects.
近期对棕色脂肪组织能量消耗能力的研究,使其成为抗肥胖治疗的一个有吸引力的靶点。我们旨在评估 L-肉碱对运动肥胖大鼠白色脂肪组织褐变的影响。60 只成年雄性 Wistar 白化大鼠,7-8 周龄,体重 130-150g,被分为 6 组,每组 10 只,实验周期为 12 周:(i)正常对照组,喂食标准脂肪饮食(SFD/对照);(ii)正常对照组,喂食标准饮食并注射 L-肉碱(250mg/kg,腹腔注射)6 周(SFD/CAR);(iii)高脂肪饮食(HFD)诱导肥胖大鼠 12 周;(iv)HFD 大鼠进行 6 周运动训练(HFD/EXE);(v)HFD 大鼠注射 L-肉碱(250mg/kg,腹腔注射)6 周(HFD/CAR);(vi)HFD 大鼠进行 6 周运动训练和 L-肉碱注射(HFD/EXE/CAR)。在 12 周实验结束时,检测体重和血清脂质谱、氧化应激和炎症标志物以及循环肌因子水平。取出比目鱼肌和腹股沟脂肪组织,测量肌肉鸢尾素、脂肪组织解偶联蛋白 1(UCP1)、CD137 和 p38MAPK 的基因表达水平以及蛋白水平。此外,对各组进行组织病理学检查。6 周运动训练和肉碱治疗均显著降低体重增加,改善肥胖引起的血脂异常,降低丙二醛(TBARS)和 TNF-α,同时增加总抗氧化能力和 IL-10。此外,血清鸢尾素水平升高,脂肪组织解偶联蛋白-1(UCP-1)、脂肪组织 CD137、p38MAPK 和肌肉纤维连接蛋白 III 型结构域蛋白 5(FNDC5)表达增加,与肉碱和运动诱导的这些生理改善相关。在联合运动和肉碱组中观察到最大的改善,表明它们对肥胖动物的有益作用具有协同作用。这些发现表明,L-肉碱可能通过刺激鸢尾素诱导脂肪组织褐变,这种现象可能与其抗氧化、抗炎和抗肥胖作用有关。