Pub Date : 2024-11-30eCollection Date: 2025-01-01DOI: 10.1080/23328940.2024.2436741
Daniel Gagnon
{"title":"Why is extreme heat associated with greater cardiovascular risk?: Comment on: Barry H, Iglesies-Grau J, Chaseling GK, Paul J, Gosselin C, D'Oliviera-sousa C, Juneau M, Harel F, Kaiser D, Pelletier-galarneau M, Gagnon D. The effect of heat exposure on myocardial blood flow and cardiovascular function. Ann Intern Med. 2024 Jul;177(7):901-910. doi: 10.7326/M24-3504.","authors":"Daniel Gagnon","doi":"10.1080/23328940.2024.2436741","DOIUrl":"10.1080/23328940.2024.2436741","url":null,"abstract":"","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"12 1","pages":"4-7"},"PeriodicalIF":0.0,"publicationDate":"2024-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875493/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143558212","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-21eCollection Date: 2024-01-01DOI: 10.1080/23328940.2024.2430091
{"title":"About the Cover.","authors":"","doi":"10.1080/23328940.2024.2430091","DOIUrl":"10.1080/23328940.2024.2430091","url":null,"abstract":"","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"11 4","pages":"W1"},"PeriodicalIF":0.0,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11583598/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142711146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-20eCollection Date: 2025-01-01DOI: 10.1080/23328940.2024.2431402
Jesse L Criddle, Kristanti W Wigati, Joao Carlos Locatelli, Juliene Goncalves Costa, Julie J Collis, Andrew Haynes, Xingwei Xu, Louise H Naylor, Shane K Maloney, James D Cotter, Robert A McLaughlin, Howard H Carter, Daniel J Green
Purpose: Recent field studies of physical exertion in challenging environmental conditions have reported dissociation between elevation in body core temperature (Tc) and successful task completion. This prompted us to further examine physiological mechanisms that might underlie variability in the response to exertional heat exposure. We hypothesized that, in response to exercise in the heat, systematic differences in central and peripheral physiological variables would be apparent between participants who successfully completed the task, versus those who became hyperthermic or symptomatic.
Methods: Thirty-eight healthy participants attempted a 120-min walk (5 km/h, 2% grade) in a climate-controlled chamber (40°C, 50%RH). At rest and at regular intervals during the walk, measures of physiological heat strain were assessed. Twenty-seven participants were Completers, seven were stopped because their Tc exceeded 39°C (Hyperthermics), and four became Symptomatic (e.g. lightheaded, headache, dizzy) and did not complete the walk.
Results: Visceral adipose tissue was higher in those who became Hyperthermic, compared to the Completers (437 ± 183 vs 245 ± 268 g; p = 0.034), despite similar height and body mass. Hyperthermics also had higher heart rate (p = 0.009), and lower end-diastolic volume (p = 0.031), and stroke volume (p = 0.031) during the early stages of walking, compared to the Completers. None of the Symptomatics reached a Tc >39°C (symptoms occurred at 38.1 ± 0.4°C), and none of the Hyperthermics reported symptoms.
Conclusions: During exertional heat exposure, adiposity and exaggerated early-stage hemodynamic responses were related to Tc elevation, but hyperthermia was not related to the development of symptoms, and baseline parameters relating to body composition and fitness were not related to symptom development.
目的:最近在具有挑战性的环境条件下体力消耗的实地研究已经报道了身体核心温度(Tc)升高与成功完成任务之间的分离。这促使我们进一步研究生理机制,这可能是对运动热暴露的反应变异性的基础。我们假设,在高温下运动的反应中,成功完成任务的参与者与体温过高或有症状的参与者之间的中枢和外周生理变量的系统性差异将是明显的。方法:38名健康参与者尝试在气候控制的室内(40°C, 50%RH)步行120分钟(5公里/小时,坡度2%)。在休息和散步期间的定期间隔,评估生理热应变的测量。27名参与者是完成者,7人因为体温超过39°C(体温过高)而停止行走,4人出现症状(如头晕、头痛、头晕)而没有完成步行。结果:与完成者相比,热疗组的内脏脂肪组织更高(437±183 g vs 245±268 g);P = 0.034),尽管身高和体重相似。与完全者相比,热疗者在步行的早期阶段也有更高的心率(p = 0.009),更低的舒张末期容积(p = 0.031)和搏量(p = 0.031)。所有症状均未达到Tc bbb - 39°C(症状发生在38.1±0.4°C),并且没有热疗者报告出现症状。结论:在运动性热暴露期间,肥胖和早期血流动力学反应夸大与Tc升高有关,但热疗与症状的发展无关,与身体成分和健康相关的基线参数与症状的发展无关。
{"title":"Physiological response to exercise in the heat: Implications for risk mitigation and adaptation.","authors":"Jesse L Criddle, Kristanti W Wigati, Joao Carlos Locatelli, Juliene Goncalves Costa, Julie J Collis, Andrew Haynes, Xingwei Xu, Louise H Naylor, Shane K Maloney, James D Cotter, Robert A McLaughlin, Howard H Carter, Daniel J Green","doi":"10.1080/23328940.2024.2431402","DOIUrl":"10.1080/23328940.2024.2431402","url":null,"abstract":"<p><strong>Purpose: </strong>Recent field studies of physical exertion in challenging environmental conditions have reported dissociation between elevation in body core temperature (T<sub>c</sub>) and successful task completion. This prompted us to further examine physiological mechanisms that might underlie variability in the response to exertional heat exposure. We hypothesized that, in response to exercise in the heat, systematic differences in central and peripheral physiological variables would be apparent between participants who successfully completed the task, versus those who became hyperthermic or symptomatic.</p><p><strong>Methods: </strong>Thirty-eight healthy participants attempted a 120-min walk (5 km/h, 2% grade) in a climate-controlled chamber (40°C, 50%RH). At rest and at regular intervals during the walk, measures of physiological heat strain were assessed. Twenty-seven participants were Completers, seven were stopped because their T<sub>c</sub> exceeded 39°C (Hyperthermics), and four became Symptomatic (e.g. lightheaded, headache, dizzy) and did not complete the walk.</p><p><strong>Results: </strong>Visceral adipose tissue was higher in those who became Hyperthermic, compared to the Completers (437 ± 183 vs 245 ± 268 g; <i>p</i> = 0.034), despite similar height and body mass. Hyperthermics also had higher heart rate (<i>p</i> = 0.009), and lower end-diastolic volume (<i>p</i> = 0.031), and stroke volume (<i>p</i> = 0.031) during the early stages of walking, compared to the Completers. None of the Symptomatics reached a T<sub>c</sub> >39°C (symptoms occurred at 38.1 ± 0.4°C), and none of the Hyperthermics reported symptoms.</p><p><strong>Conclusions: </strong>During exertional heat exposure, adiposity and exaggerated early-stage hemodynamic responses were related to T<sub>c</sub> elevation, but hyperthermia was not related to the development of symptoms, and baseline parameters relating to body composition and fitness were not related to symptom development.</p>","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"12 1","pages":"71-84"},"PeriodicalIF":0.0,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875470/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143558148","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-23eCollection Date: 2025-01-01DOI: 10.1080/23328940.2024.2408059
Lisa Klous, Hilde Teien, Sarah Hollis, Koen Levels, Appie Boonstra, Wendy Sullivan-Kwantes, François Haman, John W Castellani, Milène Catoire, Boris Kingma
Military cold weather operations (CWOs) introduce a range of challenges, including extreme temperatures, strong winds, difficult terrain, and exposure to snow, ice, and water. Personnel undertaking these missions face a heightened risk of cold weather injury (CWI), such as hypothermia, freezing cold injuries, and non-freezing cold injuries. The risk of these injuries is influenced by various factors, including age, sex, and body composition. To ensure optimal and safe performance in CWOs, it is crucial to implement effective preventive measures against CWI. This article emphasizes the most pertinent strategies for CWI prevention in CWOs. Initially, it is important to assess individual vulnerability to CWI. Education and training on CWI prevention should be provided before deployment in CWOs. During CWOs, attention should be given to crucial behaviors such as using a proper layered clothing system, recognizing the risks associated with prolonged stationary periods in cold conditions, consuming adequate calories, and staying hydrated. Additionally, environmental monitoring using tools like the windchill index and regular checks on physical status are essential. Although monitoring by itself does not prevent CWI, it can prompt necessary behavioral adjustments. Education and behavioral modifications are central to preventing CWI. Given the limited research on CWI prevention in military settings, despite the frequent occurrence of these injuries, there is a pressing need for further studies to evaluate effective preventive strategies within this specific operational framework.
{"title":"Cold weather operations: Preventive strategies in a military context.","authors":"Lisa Klous, Hilde Teien, Sarah Hollis, Koen Levels, Appie Boonstra, Wendy Sullivan-Kwantes, François Haman, John W Castellani, Milène Catoire, Boris Kingma","doi":"10.1080/23328940.2024.2408059","DOIUrl":"10.1080/23328940.2024.2408059","url":null,"abstract":"<p><p>Military cold weather operations (CWOs) introduce a range of challenges, including extreme temperatures, strong winds, difficult terrain, and exposure to snow, ice, and water. Personnel undertaking these missions face a heightened risk of cold weather injury (CWI), such as hypothermia, freezing cold injuries, and non-freezing cold injuries. The risk of these injuries is influenced by various factors, including age, sex, and body composition. To ensure optimal and safe performance in CWOs, it is crucial to implement effective preventive measures against CWI. This article emphasizes the most pertinent strategies for CWI prevention in CWOs. Initially, it is important to assess individual vulnerability to CWI. Education and training on CWI prevention should be provided before deployment in CWOs. During CWOs, attention should be given to crucial behaviors such as using a proper layered clothing system, recognizing the risks associated with prolonged stationary periods in cold conditions, consuming adequate calories, and staying hydrated. Additionally, environmental monitoring using tools like the windchill index and regular checks on physical status are essential. Although monitoring by itself does not prevent CWI, it can prompt necessary behavioral adjustments. Education and behavioral modifications are central to preventing CWI. Given the limited research on CWI prevention in military settings, despite the frequent occurrence of these injuries, there is a pressing need for further studies to evaluate effective preventive strategies within this specific operational framework.</p>","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"12 1","pages":"8-27"},"PeriodicalIF":0.0,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875484/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143557681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-16eCollection Date: 2025-01-01DOI: 10.1080/23328940.2024.2411771
Harrison T Caddy, Jesse L Criddle, Kristanti W Wigati, Howard H Carter, Lachlan J Kelsey, Alla Soloshenko, William H Morgan, Barry J Doyle, Daniel J Green
Core temperature (TC) changes, alongside exercise, affect hemodynamic responses across different conduit and microvascular beds. This study investigated impacts of ecologically valid environmental heat and exercise exposures on cerebral, skin and retinal vascular responses by combining physiological assessments alongside computational fluid dynamics (CFD) modeling. Young, healthy participants (n = 12) were exposed to environmental passive heating (PH), and heated exercise (HE) (ergometer cycling), in climate-controlled conditions (50 mins, 40°C, 50% relative humidity) while maintaining upright posture. Blood flow responses in the common carotid (CCA), internal carotid (ICA) and central retinal (CRA) arteries were assessed using Duplex ultrasound, while forearm skin microvascular blood flow responses were measured using optical coherence tomography angiography. Three-dimensional retinal hemodynamics (flow and pressure) were calculated via CFD simulation, enabling assessment of wall shear stress (WSS). TC rose following PH (+0.2°C, p = 0.004) and HE (+1.4°C, p < 0.001). PH increased skin microvascular blood flow (p < 0.001), whereas microvascular CRA flow decreased (p = 0.038), despite unchanged ICA flow. HE exacerbated these differences, with increased CCA flow (p = 0.007), unchanging ICA flow and decreased CRA flow (p < 0.001), and interactions between vascular (CCA vs. ICA p = 0.018; CCA vs. CRA p = 0.004) and microvascular (skin vs. retinal arteriolar p < 0.001) territories. Simulations revealed patterns of WSS and lumen pressure that uniformly decreased following HE. Under ecologically valid thermal challenge, different responses occur in distinct conduit and microvascular territories, with blood flow distribution favoring systemic thermoregulation, while flow may redistribute within the brain.
核心温度(TC)的变化与运动一起影响不同导管和微血管床的血流动力学反应。本研究通过结合生理评估和计算流体动力学(CFD)建模,研究了生态有效的环境热和运动暴露对大脑、皮肤和视网膜血管反应的影响。年轻健康的参与者(n = 12)在气候控制条件下(50分钟,40°C, 50%相对湿度),保持直立姿势,暴露于环境被动加热(PH)和加热运动(HE)(骑测力计)。使用双工超声评估颈总动脉(CCA)、颈内动脉(ICA)和视网膜中央动脉(CRA)的血流反应,同时使用光学相干断层扫描血管造影测量前臂皮肤微血管血流反应。通过CFD模拟计算三维视网膜血流动力学(流量和压力),从而评估壁面剪切应力(WSS)。尽管ICA流量不变,但PH(+0.2°C, p = 0.004)和HE(+1.4°C, p p p = 0.038)后TC升高。HE加剧了这些差异,CCA流量增加(p = 0.007), ICA流量不变,CRA流量减少(p = 0.018;CCA vs. CRA p = 0.004)和微血管(皮肤vs.视网膜小动脉p
{"title":"Retinal and cerebral hemodynamics redistribute to favor thermoregulation in response to passive environmental heating and heated exercise in humans.","authors":"Harrison T Caddy, Jesse L Criddle, Kristanti W Wigati, Howard H Carter, Lachlan J Kelsey, Alla Soloshenko, William H Morgan, Barry J Doyle, Daniel J Green","doi":"10.1080/23328940.2024.2411771","DOIUrl":"10.1080/23328940.2024.2411771","url":null,"abstract":"<p><p>Core temperature (T<sub>C</sub>) changes, alongside exercise, affect hemodynamic responses across different conduit and microvascular beds. This study investigated impacts of ecologically valid environmental heat and exercise exposures on cerebral, skin and retinal vascular responses by combining physiological assessments alongside computational fluid dynamics (CFD) modeling. Young, healthy participants (<i>n</i> = 12) were exposed to environmental passive heating (PH), and heated exercise (HE) (ergometer cycling), in climate-controlled conditions (50 mins, 40°C, 50% relative humidity) while maintaining upright posture. Blood flow responses in the common carotid (CCA), internal carotid (ICA) and central retinal (CRA) arteries were assessed using Duplex ultrasound, while forearm skin microvascular blood flow responses were measured using optical coherence tomography angiography. Three-dimensional retinal hemodynamics (flow and pressure) were calculated via CFD simulation, enabling assessment of wall shear stress (WSS). T<sub>C</sub> rose following PH (+0.2°C, <i>p</i> = 0.004) and HE (+1.4°C, <i>p</i> < 0.001). PH increased skin microvascular blood flow (<i>p</i> < 0.001), whereas microvascular CRA flow decreased (<i>p</i> = 0.038), despite unchanged ICA flow. HE exacerbated these differences, with increased CCA flow (<i>p</i> = 0.007), unchanging ICA flow and decreased CRA flow (<i>p</i> < 0.001), and interactions between vascular (CCA vs. ICA <i>p</i> = 0.018; CCA vs. CRA <i>p</i> = 0.004) and microvascular (skin vs. retinal arteriolar <i>p</i> < 0.001) territories. Simulations revealed patterns of WSS and lumen pressure that uniformly decreased following HE. Under ecologically valid thermal challenge, different responses occur in distinct conduit and microvascular territories, with blood flow distribution favoring systemic thermoregulation, while flow may redistribute within the brain.</p>","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"12 1","pages":"55-70"},"PeriodicalIF":0.0,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875494/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143558058","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-26eCollection Date: 2025-01-01DOI: 10.1080/23328940.2024.2406730
Yunuo Su, Emma O'Donnell, Sven P Hoekstra, Christof A Leicht
Passively elevating body temperature can trigger a potentially beneficial acute inflammatory response. However, heat therapy often causes discomfort and negative thermal perceptions, particularly in females who generally have lower heat tolerance than males. This study aimed to evaluate the impact of facial cooling on thermal comfort and interleukin-6 concentration in response to 60 minutes of dry heat exposure, and to investigate sex differences in physiological responses and perceptions. 22 healthy young adults (10 females, 12 males; age: 24.4 ± 3.3 years) completed three trials in randomized order using a dry sauna device: 1) Hyperthermia (71.1 ± 1.9°C; HEAT), 2) Hyperthermia with facial cooling via fans (71.1 ± 3.0°C; FAN), and 3) Normothermia (27.0 ± 0.9°C; CON). Blood samples to determine interleukin-6 (IL-6) plasma concentration were collected before and after exposure; basic affect and thermal comfort, rectal and skin temperature were assessed throughout the intervention. Rectal temperature following HEAT (38.0 ± 0.3°C) and FAN (37.8 ± 0.3°C) did not differ between males and females (p = 0.57). Females had higher forehead skin temperatures than males (p ≤ 0.019). Thermal comfort remained more positive in FAN compared to HEAT (p ≤ 0.002). Females felt more thermal discomfort than males in HEAT (p ≤ 0.03), but not in FAN (p = 0.28). The increase in IL-6 plasma concentration was similar between HEAT and FAN (p = 1.00), and higher than CON (p ≤ 0.02); there was no difference between males and females (p = 0.69). This study showed that facial cooling alleviated the thermal discomfort during heat exposure, particularly benefitted females, and did not impede the acute IL-6 response.
{"title":"Facial cooling improves thermal perceptions and maintains the interleukin-6 response during passive heating: A sex comparison.","authors":"Yunuo Su, Emma O'Donnell, Sven P Hoekstra, Christof A Leicht","doi":"10.1080/23328940.2024.2406730","DOIUrl":"10.1080/23328940.2024.2406730","url":null,"abstract":"<p><p>Passively elevating body temperature can trigger a potentially beneficial acute inflammatory response. However, heat therapy often causes discomfort and negative thermal perceptions, particularly in females who generally have lower heat tolerance than males. This study aimed to evaluate the impact of facial cooling on thermal comfort and interleukin-6 concentration in response to 60 minutes of dry heat exposure, and to investigate sex differences in physiological responses and perceptions. 22 healthy young adults (10 females, 12 males; age: 24.4 ± 3.3 years) completed three trials in randomized order using a dry sauna device: 1) Hyperthermia (71.1 ± 1.9°C; HEAT), 2) Hyperthermia with facial cooling via fans (71.1 ± 3.0°C; FAN), and 3) Normothermia (27.0 ± 0.9°C; CON). Blood samples to determine interleukin-6 (IL-6) plasma concentration were collected before and after exposure; basic affect and thermal comfort, rectal and skin temperature were assessed throughout the intervention. Rectal temperature following HEAT (38.0 ± 0.3°C) and FAN (37.8 ± 0.3°C) did not differ between males and females (<i>p</i> = 0.57). Females had higher forehead skin temperatures than males (<i>p</i> ≤ 0.019). Thermal comfort remained more positive in FAN compared to HEAT (<i>p</i> ≤ 0.002). Females felt more thermal discomfort than males in HEAT (<i>p</i> ≤ 0.03), but not in FAN (<i>p</i> = 0.28). The increase in IL-6 plasma concentration was similar between HEAT and FAN (<i>p</i> = 1.00), and higher than CON (<i>p</i> ≤ 0.02); there was no difference between males and females (<i>p</i> = 0.69). This study showed that facial cooling alleviated the thermal discomfort during heat exposure, particularly benefitted females, and did not impede the acute IL-6 response.</p>","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"12 1","pages":"40-54"},"PeriodicalIF":0.0,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875509/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143558140","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-24eCollection Date: 2024-01-01DOI: 10.1080/23328940.2024.2402125
Lars Nybo, Andreas D Flouris
{"title":"<i>Temperature</i>: A frontier journal in cross-scientific approaches to combat climate change.","authors":"Lars Nybo, Andreas D Flouris","doi":"10.1080/23328940.2024.2402125","DOIUrl":"10.1080/23328940.2024.2402125","url":null,"abstract":"","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"11 4","pages":"299-301"},"PeriodicalIF":0.0,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11583577/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142711142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-24eCollection Date: 2024-01-01DOI: 10.1080/23328940.2024.2401674
Anders Blomqvist
Our body temperature is normally kept within a narrow range of 1°C. For example, if our body temperature rises, such as in a hot environment or due to strenuous exercise, our thermoregulatory system will trigger a powerful heat defense response with vasodilation, sweating, and lowered metabolism. During fever, which often involves body temperatures of up to 41°C, this heat defense mechanism is apparently inhibited; otherwise, the rising body temperature would be immediately combated, and fever would not be allowed to develop. New evidence suggests how and where this inhibition takes place. In two consecutive studies from Cheng et al. and Xu et al., it has been shown that prostaglandin E2, which generates fever by acting on thermosensory neurons in the preoptic hypothalamus, also acts on neurons in the brainstem parabrachial nucleus, which receive temperature information from temperature-activated spinal cord neurons and relay this information to the thermoregulatory center in the hypothalamus to either induce cold or heat defenses. By acting on the same type of prostaglandin E2 receptor that is critical for fever generation in the preoptic hypothalamus, the EP3 receptor, prostaglandin E2 inhibits the signaling of the heat-responsive parabrachial neurons, while stimulating the cold-responsive neurons. These novel findings thus show that prostaglandin E2, by binding to the same receptor subtype in the parabrachial nucleus as in the preoptic hypothalamus, adjusts the sensitivity of the thermosensory system in a coordinated manner to allow the development of febrile body temperatures.
{"title":"Prostaglandin E<sub>2</sub> production in the brainstem parabrachial nucleus facilitates the febrile response.","authors":"Anders Blomqvist","doi":"10.1080/23328940.2024.2401674","DOIUrl":"10.1080/23328940.2024.2401674","url":null,"abstract":"<p><p>Our body temperature is normally kept within a narrow range of 1°C. For example, if our body temperature rises, such as in a hot environment or due to strenuous exercise, our thermoregulatory system will trigger a powerful heat defense response with vasodilation, sweating, and lowered metabolism. During fever, which often involves body temperatures of up to 41°C, this heat defense mechanism is apparently inhibited; otherwise, the rising body temperature would be immediately combated, and fever would not be allowed to develop. New evidence suggests how and where this inhibition takes place. In two consecutive studies from Cheng et al. and Xu et al., it has been shown that prostaglandin E<sub>2</sub>, which generates fever by acting on thermosensory neurons in the preoptic hypothalamus, also acts on neurons in the brainstem parabrachial nucleus, which receive temperature information from temperature-activated spinal cord neurons and relay this information to the thermoregulatory center in the hypothalamus to either induce cold or heat defenses. By acting on the same type of prostaglandin E<sub>2</sub> receptor that is critical for fever generation in the preoptic hypothalamus, the EP<sub>3</sub> receptor, prostaglandin E<sub>2</sub> inhibits the signaling of the heat-responsive parabrachial neurons, while stimulating the cold-responsive neurons. These novel findings thus show that prostaglandin E<sub>2</sub>, by binding to the same receptor subtype in the parabrachial nucleus as in the preoptic hypothalamus, adjusts the sensitivity of the thermosensory system in a coordinated manner to allow the development of febrile body temperatures.</p>","PeriodicalId":36837,"journal":{"name":"Temperature","volume":"11 4","pages":"309-317"},"PeriodicalIF":0.0,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11583619/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142711069","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-11eCollection Date: 2024-01-01DOI: 10.1080/23328940.2024.2394341
Fergus K O'Connor, Gregory W McGarr, Emma R McCourt, Robert D Meade, Glen P Kenny
While foot immersion and neck cooling have been recommended for protecting heat-vulnerable groups, recent evidence does not support their efficacy for mitigating increases in physiological heat strain in older adults. However, their influence on self-reported environmental symptoms and mood-state remains unclear. Seventeen older adults (nine females, median [interquartile range] age: 72 [69-74]) completed three randomized heat exposures (6-h; 38°C, 35% relative humidity) with no cooling (control), foot immersion to mid-calf in 20°C water for the final 40-min of each hour (foot immersion), or foot immersion with a wet towel (20°C) around the neck (foot immersion with neck cooling). Core temperature, skin temperature, and heart rate areas under the curve (AUC) were assessed as indicators of cumulative physiological strain. Environmental symptom scores (68-item environmental symptoms questionnaire) and mood disturbance (40-item profile of mood states questionnaire) were evaluated at end-heating (adjusted for pre-exposure). Core temperature AUC was not different between conditions (p = 0.418). However, the skin temperature and heart rate AUCs were 11.8°C · h [95% confidence interval: 8.1, 15.5] and 12.5 bpm · h [0.1, 24.8] lower for foot immersion and 16.6°C · h [12.9, 20.3] and 19.6 bpm · h [7.2, 32.0] lower for foot immersion with neck cooling compared to control (p ≤ 0.032). Environmental symptom scores were 0.8-fold [0.6, 1.0] lower for both foot immersion with and without neck cooling, compared to control (both p = 0.036). Mood disturbance was not different between conditions (both p ≥ 0.275). Foot immersion with and without neck cooling reduces self-reported environmental symptoms in older adults despite having little effect on physiological heat strain.
虽然浸脚和颈部降温被推荐用于保护易受高温影响的人群,但最近的证据并不支持它们在减轻老年人生理热负荷增加方面的功效。然而,它们对自我报告的环境症状和情绪状态的影响仍不清楚。17 名老年人(9 名女性,年龄中位数[四分位数间距]:72 [69-74])完成了三次随机热暴露(6 小时;38°C,相对湿度 35%),分别为不降温(对照组)、每小时最后 40 分钟将脚浸泡在 20°C 的水中至小腿中部(浸脚组)或用湿毛巾(20°C)围颈浸脚组(浸脚加围颈降温组)。评估核心温度、皮肤温度和心率曲线下面积(AUC),作为累积生理应变的指标。在加热结束时对环境症状评分(68 项环境症状问卷)和情绪障碍(40 项情绪状态概况问卷)进行评估(根据暴露前的情况进行调整)。核心温度 AUC 在不同条件下没有差异(p = 0.418)。然而,与对照组相比,浸泡脚的皮肤温度和心率 AUC 分别为 11.8°C - h [95% 置信区间:8.1, 15.5] 和 12.5 bpm - h [0.1, 24.8],浸泡脚加颈部降温的皮肤温度和心率 AUC 分别为 16.6°C - h [12.9, 20.3] 和 19.6 bpm - h [7.2, 32.0](p ≤ 0.032)。与对照组相比,带颈部降温的足部浸泡和不带颈部降温的足部浸泡的环境症状评分均低 0.8 倍 [0.6, 1.0](均 p = 0.036)。情绪障碍在不同条件下没有差异(均 p ≥ 0.275)。有颈部降温和无颈部降温的足部浸泡都能减轻老年人自我报告的环境症状,尽管对生理热应变影响不大。
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