Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0020440 (hypercapnia)
 7,939 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Oxygen consumption (VO2) was measured in normoxia as ambient temperature (Ta) was lowered from 40 to 15 degrees C, at the rate of 0.5 degrees C/min (thermoneutrality approximately 33 degrees C). In 2-day-old rats born in hypoxia after hypoxic gestation, the Ta-VO2 relationship was as in controls; their interscapular brown adipose tissue (IBAT) was hypoplastic (less proteins and DNA), with lower concentration of the mitochondrial uncoupling protein thermogenin. In 8-day-old rats exposed to hypoxia postnatally (day 2 to day 8), at any Ta below thermoneutrality VO2 was higher than in controls; also, in this group IBAT was hypoplastic with decreased thermogenin. Additional measurements under various experimental conditions indicated that the increased thermogenic capacity was not explained by the smaller body mass and increased blood oxygen content or by the eventuality of intermittent cold stimuli during the chronic hypoxia. On the other hand, chronic hypercapnia (3% CO2 in normoxia, from day 2 to day 8) also resulted in increased normoxic thermogenesis. We conclude that chronic hypoxia in the perinatal period 1) reduces IBAT mass and thermogenin concentration and 2) can increase the newborn's thermogenic capacity because of stress-related mechanisms not specific to hypoxia.
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PMID:Thermogenesis in newborn rats after prenatal or postnatal hypoxia. 965 59

We asked to what extent differences in caloric intake during the first postnatal weeks may modify thermal and respiratory control of 1-month old rats. Large-size (Large) and small-size (Small) rats were obtained by raising rats in, respectively, small (6 pups) and large (16 pups) litters. In Small, the rate of oxygen consumption (V(O(2))/kg) was less than in Large during the first 2-3 weeks, and higher thereafter, when the thermogenic needs to maintain body temperature (Tb) increased. At day 31, when body weight in Small was approximately 80% of Large, Small maintained Tb in the cold with higher V(O(2))/kg than Large. The total uncoupling protein of the brown adipose tissue was unchanged. Also pulmonary ventilation (VE/kg) was higher in Small, maintaining the proportionality with V(O(2)). Lung weight in Small was reduced in proportion to body weight, with higher protein-DNA ratio. The compliances of the respiratory system and lungs, normalized by body weight, and the hyperventilatory responses to hypoxia or hypercapnia, expressed as % increase in VE/V(O(2)), were similar in Small and Large. Differences between Small and Large were reduced or no longer present in a group of Small rats raised until their body weight was as in Large. We conclude that rather important developmental differences in caloric intake and metabolic level, in otherwise healthy rats, had no long-term carry over effects in the developmental processes of respiratory and thermal control, other than the effects strictly attributable to the alterations in body size.
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PMID:Thermal and respiratory control in young rats with altered caloric intake during postnatal development. 1242 69

We questioned to what extent sustained increases in metabolic rate during the neonatal period may influence the development of thermal and respiratory control. Male rats were exposed to cold (14 degrees C) for the first 3 weeks, which increased metabolic rate with small effects on body growth. Measurements were performed at 1 month of age, when the body weight of the Cold group averaged approximately 88% of Controls. In Cold rats, the concentration of the uncoupling protein of the brown adipose tissue was increased. Acute exposures to different ambient temperatures (5, 15, 25 and 35 degrees C) provoked changes in body temperature similar in Cold and in Control rats. At these temperatures, small differences in the absolute values of oxygen consumption (Vdot;(O(2))) between the two groups could be explained by the differences in body weight. Hematocrit and lung weight of Cold rats were as in Controls, but the lung protein-DNA ratio was increased because of a drop in lung cellularity. The resting ventilation-oxygen consumption ratio (Vdot;(E)/Vdot;(O(2))) was similar between Cold and Controls. Also the changes in Vdot;(O(2)) and Vdot;(E) during acute hypoxia (10% O(2)) or hypercapnia (5% CO(2)), and the corresponding hyperventilatory responses (increases in Vdot;(E)/Vdot;(O(2))) did not significantly differ between the two groups. In conclusion, in the rat, the increased metabolic requirements caused by cold exposure during the early postnatal phases improved the thermogenic capacity, while having negligible impact on the development of respiratory control.
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PMID:Thermal and respiratory control in young rats exposed to cold during postnatal development. 1254 75