Dean A Myers, Krista Singleton, Kim Hyatt, Kanchan M Kaushal, Charles A Ducsay
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引用次数: 2
摘要
我们之前报道了长期缺氧(LTH)后,绵羊胎儿表现出棕色/米色脂肪基因的表达增强。这项研究旨在确定这些变化是否在出生后保留下来。将妊娠母羊分为3组,1)对照组,海平面组,2)LTH,高海拔(3820 m, LTH- ha)组,妊娠第40天至第137天,LTH组,返回实验室,通过输注氮维持母体PO2的降低。分娩后,羔羊保持在海平面(LTH-SL)。第14天收集肾周脂肪组织,采用qRT-PCR定量mRNA。解偶联蛋白1 (UCP-1)、PPAR γ辅助激活因子1 (PGC1α)和脱碘酶2 (DIO2) mRNA水平在LTH组均显著降低,而PR结构域16 (PRDM16)水平无显著差异。与对照组相比,LTH-HA组维持过氧化物酶体增殖物激活受体(PPARγ)水平,LTH-SL组显著升高。与我们之前的LTH胎儿研究不同,与对照组相比,产后14天棕色/米色脂肪表型迅速消失,而PPARγ保持不变。这种褐色脂肪表型的丧失可能由于能量消耗减少而促进肥胖,有利于脂肪沉积。
Long term hypoxia during gestation alters perirenal adipose tissue gene expression in the lamb.
We previously reported that following long-term hypoxia (LTH), the ovine foetus exhibits enhanced expression of brown/beige adipose genes. This study was designed to determine if these changes are preserved after birth. Pregnant ewes were divided among three groups, 1) Control, sea level, 2) LTH, high altitude (3,820 m, LTH-HA) from ~ day 40 of gestation through ~14 days post-delivery and 3) LTH from ⁓ day 40 through day 137 of gestation then returned to the laboratory where atory reduced maternal PO2 was maintained by nitrogen infusion. Following delivery, lambs remained at sea level (LTH-SL). Perirenal adipose tissue was collected at ~day 14, and qRT-PCR was used to quantify mRNA. Uncoupling protein 1 (UCP-1), PPAR gamma coactivator 1 (PGC1α), and deiodinase-2 (DIO2) mRNA levels were significantly lower in both LTH groups while PR domain containing 16 (PRDM16) levels did not differ. Peroxisome proliferator-activated receptor (PPARγ) was maintained in the LTH-HA group and significantly increased in the LTH-SL group, compared to control. Unlike our previous LTH foetal studies, the brown/beige fat phenotype was rapidly lost by day 14 postpartum compared to control, while PPARγ was maintained. This loss of the brown fat phenotype may promote obesity due to decreased energy expenditure, favouring fat deposition.
期刊介绍:
Adipocyte recognizes that the adipose tissue is the largest endocrine organ in the body, and explores the link between dysfunctional adipose tissue and the growing number of chronic diseases including diabetes, hypertension, cardiovascular disease and cancer. Historically, the primary function of the adipose tissue was limited to energy storage and thermoregulation. However, a plethora of research over the past 3 decades has recognized the dynamic role of the adipose tissue and its contribution to a variety of physiological processes including reproduction, angiogenesis, apoptosis, inflammation, blood pressure, coagulation, fibrinolysis, immunity and general metabolic homeostasis. The field of Adipose Tissue research has grown tremendously, and Adipocyte is the first international peer-reviewed journal of its kind providing a multi-disciplinary forum for research focusing exclusively on all aspects of adipose tissue physiology and pathophysiology. Adipocyte accepts high-profile submissions in basic, translational and clinical research.