Timing of acute cold exposure determines UCP1 and FGF21 expression - Possible interactions between the thermal environment, thermoregulatory responses, and peripheral clocks

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Phong KT. Chau , Elin Ryan , Knut Tomas Dalen , Fred Haugen
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引用次数: 0

Abstract

Thermoregulation is synchronized across the circadian cycle to uphold thermal homeostasis. To test if time-of-day matters for the response to environmental cold exposure, mice were acclimated to thermoneutrality (27 °C) for 2 months were subjected acutely (8 h) to cold ambient conditions (15 °C), whereas controls were maintained at thermoneutral conditions. The thermal exposure was tested in separate groups (N = 8) at three distinct time-of-day periods: in the LIGHT phase (L); the DARK phase (D); and a mix of the two (D + L). The magnitude of UCP1 protein and mRNA induction in brown adipose tissue (BAT) in response to acute cold exposure was time-of-day sensitive, peaking in LIGHT, whereas lower induction levels were observed in D + L, and DARK. Plasma levels of FGF21 were induced 3-fold by acute cold exposure at LIGHT and D + L, compared to the time-matched thermoneutral controls, whereas cold in DARK did not cause a significant increase of FGF21 plasma levels. Cold exposure affected, in BAT, the temporal mRNA expression patterns of core circadian clock components: Bmal1, Clock, Per1, Per3, Cry1, Cry2 Nr1d1, and Nr1d2, but in the liver, none of the transcripts were modified. Behavioral assessment using the Thermal Gradient Test (TGT) showed that acute cold exposure reduced cold sensitivity in D + L, but not in DARK. RNA-seq analyses of somatosensory neurons in DRG highlighted the role of the core circadian components in these cells, as well as transcriptional changes due to acute cold exposure. This elucidates the sensory system as a gauge and potential regulator of thermoregulatory responses based on circadian physiology. In conclusion, acute cold exposure elicits time-of-day specific effects on thermoregulatory pathways, which may involve underlying changes in thermal perception. These results have implications for efforts aimed at reducing risks associated with the organization of shift work in cold environments.

急性寒冷暴露的时间决定了 UCP1 和 FGF21 的表达--热环境、体温调节反应和外周时钟之间可能存在相互作用。
热调节在昼夜周期中同步进行,以维持热平衡。为了测试不同时间段对环境寒冷暴露的反应是否有影响,将适应恒温(27 °C)2 个月的小鼠急性(8 小时)置于寒冷的环境条件(15 °C)下,而对照组则保持在恒温条件下。在三个不同的日间时段,分别对不同组(N = 8)进行了热暴露测试:光照阶段(L);黑暗阶段(D);以及两者混合阶段(D + L)。棕色脂肪组织(BAT)中的 UCP1 蛋白和 mRNA 对急性冷暴露的诱导程度对时间敏感,在 "光照 "阶段达到峰值,而在 "D + L "和 "黑暗 "阶段诱导程度较低。与时间匹配的恒温对照组相比,在光照和D + L条件下,急性冷暴露诱导的血浆FGF21水平是恒温对照组的3倍,而在黑暗条件下,冷暴露不会导致血浆FGF21水平的显著增加。在 BAT 中,寒冷暴露影响了昼夜节律核心成分 mRNA 的时间表达模式:Bmal1、Clock、Per1、Per3、Cry1、Cry2 Nr1d1和Nr1d2,但在肝脏中,这些转录本都没有改变。使用热梯度试验(TGT)进行的行为评估表明,急性冷暴露降低了 D + L 的冷敏感性,但没有降低 DARK 的冷敏感性。对DRG中的躯体感觉神经元进行的RNA-seq分析强调了昼夜节律核心成分在这些细胞中的作用,以及急性冷暴露引起的转录变化。这阐明了感觉系统是基于昼夜节律生理学的体温调节反应的测量器和潜在调节器。总之,急性寒冷暴露会对体温调节途径产生特定时间的影响,这可能涉及热感知的潜在变化。这些结果对减少在寒冷环境中组织轮班工作的相关风险具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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