Tankersley C G, Elston R C, Schnell A H
Department of Environmental Health Sciences, School of Hygiene and Public Health, The Johns Hopkins University, Baltimore, MD 21205, USA.
J Appl Physiol (1985). 2000 Jun;88(6):2310-8. doi: 10.1152/jappl.2000.88.6.2310.
Acutely lowering ambient O(2) tension increases ventilation in many mammalian species, including humans and mice. Inheritance patterns among kinships and between mouse strains suggest that a robust genetic influence determines individual hypoxic ventilatory responses (HVR). Here, we tested specific genetic hypotheses to describe the inheritance patterns of HVR phenotypes among two inbred mouse strains and their segregant and nonsegregant progeny. Using whole body plethysmography, we assessed the magnitude and pattern of ventilation in C3H/HeJ (C3) and C57BL/6J (B6) progenitor strains at baseline and during acute (3-5 min) hypoxic [mild hypercapnic hypoxia, inspired O(2) fraction (FI(O(2))) = 0.10] and normoxic (mild hypercapnic normoxia, FI(O(2)) = 0.21) inspirate challenges in mild hypercapnia (inspired CO(2) fraction = 0.03). First- and second-filial generations and two backcross progeny were also studied to assess response distributions of HVR phenotypes relative to the parental strains. Although the minute ventilation (VE) during hypoxia was comparable between the parental strains, breathing frequency (f) and tidal volume were significantly different; C3 mice demonstrated a slow, deep HVR relative to a rapid, shallow phenotype of B6 mice. The HVR profile in B6C3F(1)/J mice suggested that this offspring class represented a third phenotype, distinguishable from the parental strains. The distribution of HVR among backcross and intercross offspring suggested that the inheritance patterns for f and VE during mild hypercapnic hypoxia are consistent with models that incorporate two genetic determinants. These results further suggest that the quantitative genetic expression of alleles derived from C3 and B6 parental strains interact to significantly attenuate individual HVR in the first- and second-filial generations. In conclusion, the genetic control of HVR in this model was shown to exhibit a relatively simple genetic basis in terms of respiratory timing characteristics.
急性降低环境氧分压会增加包括人类和小鼠在内的许多哺乳动物的通气量。亲属之间以及小鼠品系之间的遗传模式表明,强大的遗传影响决定了个体的低氧通气反应(HVR)。在此,我们测试了特定的遗传假设,以描述两种近交小鼠品系及其分离和非分离后代中HVR表型的遗传模式。使用全身体积描记法,我们评估了C3H/HeJ(C3)和C57BL/6J(B6)亲本品系在基线以及急性(3 - 5分钟)低氧[轻度高碳酸血症性低氧,吸入氧分数(FI(O₂)) = 0.10]和常氧(轻度高碳酸血症性常氧,FI(O₂) = 0.21)吸入挑战期间(轻度高碳酸血症,吸入二氧化碳分数 = 0.03)的通气量大小和模式。还研究了第一代和第二代子代以及两个回交后代,以评估HVR表型相对于亲本品系的反应分布。尽管低氧期间的分钟通气量(VE)在亲本品系之间相当,但呼吸频率(f)和潮气量有显著差异;相对于B6小鼠的快速、浅呼吸表型,C3小鼠表现出缓慢、深的HVR。B6C3F₁/J小鼠的HVR特征表明,这一后代类别代表了第三种表型,与亲本品系不同。回交和杂交后代中HVR的分布表明,轻度高碳酸血症性低氧期间f和VE的遗传模式与包含两个遗传决定因素的模型一致。这些结果进一步表明,来自C3和B6亲本品系的等位基因的定量遗传表达相互作用,在第一代和第二代子代中显著减弱个体HVR。总之,在这个模型中,HVR的遗传控制在呼吸时间特征方面表现出相对简单的遗传基础。