[Effect of chronic hypobaric hypoxia on circulatory function in rats with different susceptibilities].
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Biomedical subjects
Publications and source records attributed to Y N Cai.
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Two strains of rats, one that adapts successfully to high altitude (HA) (Madison = M) and the other that adapts poorly and suffers a high mortality rate at high altitude (Hilltop = H) were studied during 40 days of exposure to a simulated altitude of 18 000 ft (5450 m; PB = 175). The time rate of change of blood volume (TBV), red cell volume (RBCV), plasma volume (PV) and hematocrit (Hct), and the interrelationships of these variables, particularly emphasizing TBV, PV and Hct as functions of RBCV, were compared in the M and H strains. Sea level control values in the two strains were not different, but by the 5th day at HA RBCV and TBV had expanded to a greater extent in H than M - a difference that was maintained throughout the 40 days - but PV decreased similarly in the two strains. By 30 days the inter-strain differences of RBCV, TBV, and Hct became more pronounced but still no difference of PV was noted. The most significant feature was the greater polycythemic response of H, which at the extreme range was not associated with any further decrease of PV and therefore resulted in rapid expansion of TBV. The probable effects of these responses on cardiovascular function and oxygen transport are discussed, comparing the differences of H and M strains, which became maladaptive in H. The similarity of the responses in H to those of man with chronic mountain sickness is noted.
In conscious rabbits with arterial, central venous, and cisterna magna catheters, we infused HCl, Hlactate, and Hacetate so as to lower and maintain plasma [HCO3-] at the same mean values in all three groups over 6 h. The hypothesis was that the cerebrospinal fluid (CSF) [HCO3-] will depend on the changes in CO2 partial pressure (PCO2) and be determined by the net increase in the CSF concentration of the strong anion of the acid. The delta CSF [HCO3-] did correlate strongly with the delta PCO2, with the largest decrease in CSF [HCO3-] and PCO2 being in the Hacetate group, a response we attribute to a greater stimulatory effect of Hacetate on the alveolar ventilation relative to CO2 production. However, the delta CSF [HCO3-] was not simply determined in all cases by the increase in the CSF concentration of the strong anion of the acid. In HCl acidosis, statistically delta CSF [HCO3-] was equal to delta CSF [Cl-]. In H lactate acidosis delta CSF [HCO3-] was equal to the sum of a small positive delta CSF [lactate] and a small positive delta CSF [Cl-]. In Hacetate acidosis, delta CSF [HCO3-] was equal to the sum of a large positive delta CSF [acetate] and a small negative delta CSF [Cl-]. We hypothesize that in metabolic acidosis the changes in large cavity CSF [HCO3-] depend on changes in the PCO2. The strong anion regulated by the PCO2 changes is Cl-.(ABSTRACT TRUNCATED AT 250 WORDS)
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