Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
PLoS One. 2011 May 4;6(5):e19731. doi: 10.1371/journal.pone.0019731.
Non-human primates (NHP) are now being considered as models for investigating human metabolic diseases including diabetes. Analyses of cholesterol and triglycerides in plasma derived from NHPs can easily be achieved using methods employed in humans. Information pertaining to other lipid species in monkey plasma, however, is lacking and requires comprehensive experimental analysis.
METHODOLOGIES/PRINCIPAL FINDINGS: We examined the plasma lipidome from 16 cynomolgus monkey, Macaca fascicularis, using liquid chromatography coupled with mass spectrometry (LC/MS). We established novel analytical approaches, which are based on a simple gradient elution, to quantify polar lipids in plasma including (i) glycerophospholipids (phosphatidylcholine, PC; phosphatidylethanolamine, PE; phosphatidylinositol, PI; phosphatidylglycerol, PG; phosphatidylserine, PS; phosphatidic acid, PA); (ii) sphingolipids (sphingomyelin, SM; ceramide, Cer; Glucocyl-ceramide, GluCer; ganglioside mannoside 3, GM3). Lipidomic analysis had revealed that the plasma of human and cynomolgus monkey were of similar compositions, with PC, SM, PE, LPC and PI constituting the major polar lipid species present. Human plasma contained significantly higher levels of plasmalogen PE species (p<0.005) and plasmalogen PC species (p<0.0005), while cynomolgus monkey had higher levels of polyunsaturated fatty acyls (PUFA) in PC, PE, PS and PI. Notably, cynomolgus monkey had significantly lower levels of glycosphingolipids, including GluCer (p<0.0005) and GM(3) (p<0.0005), but higher level of Cer (p<0.0005) in plasma than human. We next investigated the biochemical alterations in blood lipids of 8 naturally occurring diabetic cynomolgus monkeys when compared with 8 healthy controls.
For the first time, we demonstrated that the plasma of human and cynomolgus monkey were of similar compositions, but contained different mol distribution of individual molecular species. Diabetic monkeys exhibited decreased levels of sphingolipids, which are microdomain-associated lipids and are thought to be associated with insulin sensitivity. Significant increases in PG species, which are precursors for cardiolipin biosynthesis in mitochondria, were found in fasted diabetic monkeys (n = 8).
非人类灵长类动物(NHP)现在被认为是研究人类代谢疾病(包括糖尿病)的模型。使用在人类中使用的方法可以轻松分析来自 NHP 的血浆中的胆固醇和甘油三酯。然而,有关猴子血浆中其他脂质种类的信息尚不清楚,需要进行全面的实验分析。
方法/主要发现:我们使用液相色谱-质谱联用(LC/MS)分析了 16 只食蟹猴(Macaca fascicularis)的血浆脂质组。我们建立了新的分析方法,这些方法基于简单的梯度洗脱,可定量包括(i)甘油磷脂(磷脂酰胆碱,PC;磷脂酰乙醇胺,PE;磷脂酰肌醇,PI;磷脂酰甘油,PG;磷脂酰丝氨酸,PS;磷脂酸,PA)在内的血浆极性脂质;(ii)鞘脂(神经鞘磷脂,SM;神经酰胺,Cer;神经酰胺葡糖苷,GlcCer;神经节苷脂 Mannoside 3,GM3)。脂质组学分析表明,人类和食蟹猴的血浆具有相似的组成,PC、SM、PE、LPC 和 PI 构成了主要的极性脂质种类。人血浆中含有明显更高水平的脑苷脂 PE 种类(p<0.005)和脑苷脂 PC 种类(p<0.0005),而食蟹猴的 PC、PE、PS 和 PI 中的多不饱和脂肪酸酰基(PUFA)水平更高。值得注意的是,食蟹猴的糖脂,包括 GlcCer(p<0.0005)和 GM(3)(p<0.0005)水平明显低于人类,但血浆中的神经酰胺(Cer)水平明显高于人类(p<0.0005)。接下来,我们研究了 8 只自然发生的糖尿病食蟹猴与 8 只健康对照相比时血液脂质的生化变化。
我们首次证明,人类和食蟹猴的血浆具有相似的组成,但含有不同的个体分子种类的摩尔分布。糖尿病猴子表现出鞘脂水平降低,鞘脂是与胰岛素敏感性相关的微区相关脂质。在禁食的糖尿病猴子(n=8)中发现 PG 种类显著增加,PG 种类是线粒体中心磷脂生物合成的前体。