首页> 美国卫生研究院文献>Journal of the Endocrine Society >SAT-583 Assessment of Thermoregulatory Pathways Induced in Male and Female Mice Lacking Pituitary Adenylate Cyclase Activating Polypeptide (PACAP) in Response to Cold Acclimation
【2h】

SAT-583 Assessment of Thermoregulatory Pathways Induced in Male and Female Mice Lacking Pituitary Adenylate Cyclase Activating Polypeptide (PACAP) in Response to Cold Acclimation

机译:SAT-583在缺乏垂体腺苷酸环酶活化多肽(PACAP)的男性和雌性小鼠中诱导的热调节途径的评估响应于冷适应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pituitary Adenylate Cyclase Activating Polypetptide (PACAP) is a peptide hormone known to regulate energy homeostasis1. Mice lacking PACAP are cold sensitive and have impaired adrenergic-induced thermogenesis2-4. Interestingly, Pacap null mice can survive cold housing if acclimated slowly, similar to what was observed in UCP1 deficient mice4,5. We hypothesized that Pacap-/- mice employ alternate thermogenic pathways to compensate for impaired adaptive thermogenesis and assessed shivering thermogenesis and UCP1-dependent and UCP1-independent adaptive thermogenesis in male and female Pacap-/- and Pacap+/+ with cold acclimation (4°C). Assessment of oxidative fibres in skeletal muscles and behavioural observations did not show evidence of prolonged shivering in male or female Pacap-/- mice during cold acclimation compared to Pacap+/+ mice. We did however observe morphological and molecular differences in adipose tissues of Pacap-/- mice compared to Pacap+/+ mice that were distinct in males and females. Cold-acclimated, female Pacap-/- mice had decreased induction of UCP1 protein in intrascapular brown fat (iBAT), yet had a significantly higher beiging and UCP1 immunoreactivity (ir) in gonadal white fat (gWAT) compared to female Pacap+/+ mice. Furthermore, beiging was observed in inguinal white fat (ingWAT) and gWAT of female Pacap-/- mice housed at thermoneutrality (30°C), a finding not observed in Pacap+/+ control mice. Unlike female mice, we did not observe impaired UCP1 induction in iBAT of male Pacap-/- mice compared to Pacap+/+ mice, and this was associated with negligible UCP1-ir in male gWAT similar to wildtype controls. Despite previous work that has established impaired adaptive thermogenesis in Pacap-/- mice4, we show here that UCP1 protein can be induced in adipose tissues of Pacap-/- mice during cold acclimation, although to a lesser degree or in a different pattern compared to Pacap+/+ control mice. Taken together, this work suggests that while PACAP is clearly involved in regulating thermoregulation, it is not required for cold-induced UCP1 expression. In addition, this work highlights sexual dimorphism in adipose tissue remodeling and induction of thermogenesis with cold acclimation. References: (1) Rudecki AP, et al. Trends Endocrinol Metab. 2016;27(9), 620–632. (2) Gray SL, et al. J Mol Endocrinol. 2001;15(10), 1739–1747. (3) Gray SL, et al. J Endocrinol. 2002;143(10), 3946–3954. (4) Diané A, et al. J Endocrinol. 2014;222, 327–339. (5) Golozoubova V, et al. FASEB J. 2001;15, 2048–2050.
机译:垂体腺苷酸环酶活化聚吡啶虫(PACAP)是众所周知的肽激素,用于调节能量稳态术1。小鼠缺乏睡眠是冷敏感的,肾上腺素能诱导的热生成2-4受损。有趣的是,如果缓慢地适应缓慢,PACAP含氟小鼠可以存活冷壳体,类似于UCP1缺陷的小鼠中观察到的内容。我们假设PACAP - / - 小鼠采用交替的热原途径来补偿适应性的热生成受损,并评估阳性和女性PACAP中的颤动的热生成和UCP1依赖性和UCP1无关的适应性热量,具有冷适应的阳性和雌性PACAP - 和PACAP + / +(4° C)。与PACAP + / +小鼠相比,骨骼肌中氧化纤维和行为观察中的氧化纤维的评估并未显示在冷驯化过程中延长致血或雌性PAPAP - / - 小鼠的证据。然而,与在雄性和女性中不同的PACAP + / +小鼠相比,观察PACAP - / - 小鼠的脂肪组织的形态和分子差异。冷适应的雌性PACAP - / - 小鼠在脑脑膜棕色脂肪(IBAT)中诱导UCP1蛋白(IBAT),而与雌性PACAP + / +小鼠相比,Gonadal白脂(GWAT)具有显着更高的凸起和UCP1免疫反应性(IR) 。此外,在腹股沟白脂(Ingwat)中观察到凸起,并且在热屈臣氏(30°C)的雌性PACAP - / - 小鼠的Gwat,在PACAP + / +对照小鼠中观察到未观察到的发现。与女性小鼠不同,与PACAP + / +小鼠相比,我们没有观察到雄性PACAP - / - 小鼠Ibat中的UCP1诱导,这与雄性GWAT中的可忽略的UCP1-IR相关联。尽管以前在PACAP - / - MICE4中建立了适应性的自发性受损的工作,但我们展示了UCP1蛋白在冷驯化期间PACAP - / - 小鼠的脂肪组织中可以诱导,尽管与较小程度或不同的模式Pacap + / +控制小鼠。在一起,这项工作表明,虽然PACAP明显参与调节温度调节,但不需要冷诱导的UCP1表达。此外,这项工作突出了脂肪组织重塑的性二态性和诱导热处理的诱导。参考文献:(1)Rudecki AP,等人。趋势内分泌代理。 2016; 27(9),620-632。 (2)灰色sl,等。 J mol内分泌。 2001; 15(10),1739-1747。 (3)灰色sl,等。 J内切蛋白。 2002; 143(10),3946-3954。 (4)DianéA等人。 J内切蛋白。 2014; 222,327-339。 (5)Golezoubova v等。 Faseb J. 2001; 15,2048-2050。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号