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Am J Physiol Regul Integr Comp Physiol 292: R103-R108, 2007. First published May 25, 2006; doi:10.1152/ajpregu.00074.2006
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Physiology and Pharmacology of Temperature Regulation

Impaired defense of core temperature in aged humans during mild cold stress

David W. DeGroot1 and W. Larry Kenney1,2

1Intercollege Graduate Degree Program in Physiology and 2Noll Laboratory, Department of Kinesiology, Pennsylvania State University, University Park, Pennsylvania

Submitted 27 January 2006 ; accepted in final form 18 May 2006

Aged humans often exhibit an impaired defense of core temperature during cold stress. However, research documenting this response has typically used small subject samples and strong cold stimuli. The purpose of this study was to determine the responses of young and older subjects, matched for anthropometric characteristics, during mild cold stress. Thirty-six young (YS; 23 ± 1 years, range 18–30) and 46 older (OS; 71 ± 1 years, range 65–89) subjects underwent a slow transient cold air exposure from a thermoneutral baseline, during which esophageal (Tes) and mean skin temperatures (Tsk), O2 consumption, and skin blood flow (SkBF; laser-Doppler flowmetry) were measured. Cold exposure was terminated at the onset of visible sustained shivering. Net metabolic heat production (Mnet), heat debt, predicted change in midregion temperature ({Delta}Tmid), and tissue insulation (It) were calculated. Cutaneous vascular conductance (CVC) was calculated as laser-Doppler flux/mean arterial pressure and expressed as percent change from baseline ({Delta}CVC%base). There were no baseline group differences for Tes, but OS Mnet was lower (OS: 38.0 ± 1.1; YS: 41.9 ± 1.1 W · m–2, P < 0.05). Tes was well maintained in YS but fell progressively in OS (P < 0.01 for all timepoints after 35 min). The skin vasoconstrictor response to mild cold stress was attenuated in OS (42 ± 3 vs. 53 ± 4 {Delta}CVC%base, P < 0.01). There were no group differences for Tsk or It, while Mnet remained lower in OS (P < 0.05). The {Delta}Tmid did not account for the drop in Tes in OS. Healthy aged humans failed to maintain Tes; however, the mechanisms underlying this response are not clear.

skin blood flow; core temperature



Address for reprint requests and other correspondence: D. W. DeGroot, 229 Noll Laboratory, The Pennsylvania State Univ., Univ. Park, PA 16802 (e-mail: dwd141{at}psu.edu)




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