Vail Gwyndolin M, Walley Sabrina N, Yasrebi Ali, Maeng Angela, Degroat Thomas J, Conde Kristie M, Roepke Troy A
Joint Graduate Program in Toxicology, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Department of Animal Sciences, School of Environmental & Biological Sciences, Rutgers, the State University of New Jersey, New Brunswick, NJ, USA.
J Toxicol Environ Health A. 2022 May 3;85(9):381-396. doi: 10.1080/15287394.2021.2023716. Epub 2022 Jan 9.
Previously, organophosphate flame retardants (OPFRs) were demonstrated to dysregulate homeostatic parameters of energy regulation within an adult mouse model of diet-induced obesity. Using the same OPFR mixture consisting of 1 mg/kg/day of each triphenyl phosphate, tricresyl phosphate, and tris(1,3-dichloro-2-propyl)phosphate, the current study examined the role of peroxisome proliferator-activated receptor gamma (PPARγ) in OPFR-induced disruption by utilizing mice with brain-specific deletion of PPARγ (PPARγKO) fed either a low-fat diet (LFD) or high-fat diet (HFD). Body weight and composition, feeding behavior, glucose and insulin tolerance, circulating peptide hormones, and expression of hypothalamic genes associated with energy homeostasis were recorded. When fed HFD, the effects of OPFR on body weight and feeding behavior observed in the previous wild-type (WT) study were absent in mice lacking neuronal PPARγ. This posits PPARγ as an important target for eliciting OPFR disruption in a diet-induced obesity model. Interestingly, female PPARγKO mice, but not males, experienced many novel OPFR effects not noted in WT mice, including decreased fat mass, altered feeding behavior and efficiency, improved insulin sensitivity, elevated plasma ghrelin and hypothalamic expression of its receptor. Taken together, these data suggest both direct roles for PPARγ in OPFR disruption of obese mice and indirect sensitization of pathways alternative to PPARγ when neuronal expression is deleted.
此前,在饮食诱导肥胖的成年小鼠模型中,有机磷酸酯阻燃剂(OPFRs)被证明会破坏能量调节的稳态参数。本研究使用由磷酸三苯酯、磷酸三甲苯酯和磷酸三(1,3-二氯-2-丙基)酯各1 mg/kg/天组成的相同OPFR混合物,通过对喂食低脂饮食(LFD)或高脂饮食(HFD)的脑特异性缺失过氧化物酶体增殖物激活受体γ(PPARγ)的小鼠(PPARγKO)进行实验,研究了PPARγ在OPFR诱导的破坏作用中的角色。记录了体重和组成、进食行为、葡萄糖和胰岛素耐受性、循环肽激素以及与能量稳态相关的下丘脑基因的表达。当喂食HFD时,在先前野生型(WT)研究中观察到的OPFR对体重和进食行为的影响在缺乏神经元PPARγ的小鼠中未出现。这表明PPARγ是饮食诱导肥胖模型中引发OPFR破坏的重要靶点。有趣的是,雌性PPARγKO小鼠而非雄性小鼠出现了许多在WT小鼠中未观察到的新型OPFR效应,包括脂肪量减少、进食行为和效率改变以及胰岛素敏感性提高、血浆胃饥饿素升高及其受体在下丘脑中的表达增加。综上所述,这些数据表明PPARγ在肥胖小鼠的OPFR破坏中具有直接作用,并且在神经元表达缺失时,PPARγ替代途径存在间接致敏作用。