Ambient temperature modulates hypoxic-induced changes in rat body temperature and activity differentially

Citation
B. Bishop et al., Ambient temperature modulates hypoxic-induced changes in rat body temperature and activity differentially, AM J P-REG, 280(4), 2001, pp. R1190-R1196
Citations number
23
Categorie Soggetti
Physiology
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
ISSN journal
03636119 → ACNP
Volume
280
Issue
4
Year of publication
2001
Pages
R1190 - R1196
Database
ISI
SICI code
0363-6119(200104)280:4<R1190:ATMHCI>2.0.ZU;2-4
Abstract
When rats, acclimated to an ambient temperature (T-a) of 29 degreesC, are e xposed to 10% O-2 for 63 h, the circadian rhythms of body temperature (T-b) and level of activity (L-a) are abolished, Tb falls to a hypothermic nadir followed by a climb to a hyperthermic peak, L-a remains depressed (Bishop B, Silva G, Krasney J, Salloum A, Roberts A, Nakano H, Shucard D, Rifkin D, and Farkas G. Am J Physiol Regulatory Integrative Comp Physiol 279: R1378- R1389, 2000), and overt brain pathology is detected (Krasney JA, Farkas G, Shucard DW, Salloum AC, Silva G, Roberts A, Rifkin D, Bishop B, and Rubio A . Soc Neurosci Abstr 25: 581, 1999). To determine the role of T-a in these hypoxic-induced responses, T-b and L-a data were detected by telemetry ever y 15 min for 48 h on air, followed by 63 h on 10% O2 from rats acclimated t o 25 or 21 degreesC. Magnitudes and rates of decline in T-b after onset of hypoxia were inversely proportional to T-a, whereas magnitudes and rates of T-b climb after the hypothermic nadir were directly proportional to T-a. N o hyperthermia, so prominent at 29 degreesC, occurred at 25 or 21 degreesC. The hypoxic depression of L-a was least at 21 degreesC and persisted throu ghout the hypoxia. In contrast, T-a was a strong determinant of the magnitu des and time courses of the initial fall and subsequent rise in T-b. We pro pose that the absence of hyperthermia at 21 and 25 degreesC as well as a pe rsisting hypothermia may protect the brain from overt pathology.