Maria Pia de la Maza, Institute of Nutrition and Food Technology, Human Nutrition, El Libano 5524, Santiago, 7830490, Chile, Tel: 56229781502, mobile: 56988894245, Fax: 56222214030,
J Nutr Health Aging. 2015 Apr;19(4):389-96. doi: 10.1007/s12603-014-0548-7.
Obesity is a risk factor for diabetes and its consequences, including accelerated ageing and mortality. The underlying factor could be accumulation of certain lipid moieties, such as ceramides (CER) and diacylgycerol (DAG) within muscle tissue, which are known to promote insulin resistance (IR), induce inflammation and oxidative injury, ultimately altering muscle function.
First, to study the relationship between body composition and age (independent variables) with skeletal muscle accumulation of lipid species, oxidative injury and strength. Second, to analyze the relationship between muscle tissue metabolites and insulin resistance, inflammation and lymphocyte telomere length, the latter as an indicator of ageing.
The sample included 56 healthy sedentary males, scheduled for inguinal hernia surgery, aged 27 to 80 y. Each individual was subject to anthropometric measurements, body composition assessment through radiologic densitometry (DEXA), measurement of handgrip and quadriceps strength, serum biochemical parameters (lipoproteins, creatinine, high sensitivity C reactive protein [hsCRP], fasting and post glucose insulin and glucose concentrations for calculation of IR through the Matsuda and HOMA-IR indexes), and extraction of peripheral leukocytes for measurement of telomere length. During the surgical procedure, a sample of muscle tissue was obtained (anterior abdominal oblique) in order to measure CER and DAG (and sub species according to chain length and saturation) by mass spectrometry, 4 hydroxy-2-nonenal adducts (4-HNE) using electron microscopy immunohistochemistry, and carboxymethyl-lisine (CML) by immunohistochemistry, the latter as indicators of oxidative stress (OS).
Body mass index (BMI) of twenty six individuals was > 25 k/m2, while BMI of 7 was > 30 k/m2. Overweight/obese individuals, did not exhibit differences in skeletal muscle lipid metabolites, however total CER and specific long chain CER sub-species (20 and 22 carbon) increased significantly among individuals with a central fat distribution (n = 14) as well as in glucose intolerant subjects (n =23). A negative association was found between mononuclear leukocyte telomere length and 20 and 22 carbon CER (rho = - 0.4 and -0.5 0 p < 0.05). Muscle strength was not associated with any of the measured muscle metabolites or markers of OS. A multiple regression analysis accepted central abdominal fat and telomere length as significant predictors of CER (R2 = 0.28).
An association was found between accumulation of specific ceramide species in muscle tissue and abdominal obesity, glucose intolerance and shortening of leukocyte telomeres, although not with muscle oxidative injury or dysfunction.
肥胖是糖尿病及其后果(包括加速衰老和死亡)的一个风险因素。潜在因素可能是肌肉组织内某些脂质成分(如神经酰胺[CER]和二酰基甘油[DAG])的积累,这些成分已知会促进胰岛素抵抗(IR),诱导炎症和氧化损伤,最终改变肌肉功能。
首先,研究身体成分和年龄(自变量)与骨骼肌脂质成分、氧化损伤和强度的关系。其次,分析肌肉组织代谢物与胰岛素抵抗、炎症和淋巴细胞端粒长度的关系,后者作为衰老的指标。
该样本包括 56 名健康的久坐男性,计划接受腹股沟疝手术,年龄 27 至 80 岁。每位个体都接受了人体测量学测量、通过放射密度测定法(DEXA)进行的身体成分评估、握力和股四头肌强度测量、血清生化参数(脂蛋白、肌酐、高敏 C 反应蛋白[hsCRP]、空腹和葡萄糖后胰岛素和葡萄糖浓度,通过 Matsuda 和 HOMA-IR 指数计算 IR)以及外周白细胞的提取,以测量端粒长度。在手术过程中,获取了(前腹斜肌)肌肉组织样本,通过质谱法测量 CER 和 DAG(根据链长和饱和度测量亚种)、电子显微镜免疫组织化学测量 4-羟基-2-壬烯醛加合物(4-HNE),以及免疫组织化学测量羧甲基赖氨酸(CML),后者作为氧化应激(OS)的指标。
26 人的 BMI>25 k/m2,而 7 人的 BMI>30 k/m2。超重/肥胖个体的骨骼肌脂质代谢物没有差异,但在具有中央脂肪分布的个体(n=14)和葡萄糖不耐受的个体(n=23)中,总 CER 和特定长链 CER 亚种(20 和 22 个碳原子)显著增加。单核白细胞端粒长度与 20 和 22 个碳原子 CER 呈负相关(rho=-0.4 和-0.5,p<0.05)。肌肉强度与任何测量的肌肉代谢物或 OS 标志物均无关。多元回归分析接受中央腹部脂肪和端粒长度为 CER 的显著预测因子(R2=0.28)。
肌肉组织中特定神经酰胺种类的积累与腹部肥胖、葡萄糖不耐受和白细胞端粒缩短有关,但与肌肉氧化损伤或功能障碍无关。