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法瘦素受体突变与棕色挪威大鼠和祖克大鼠杂交后代呼吸频率的遗传力。

The fa leptin receptor mutation and the heritability of respiratory frequency in a Brown Norway and Zucker intercross.

作者信息

Iyengar Sudha K, Stein Catherine M, Russo Karlie, Erokwu Bernadette O, Strohl Kingman P

机构信息

Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

J Appl Physiol (1985). 2004 Sep;97(3):811-20. doi: 10.1152/japplphysiol.01187.2003. Epub 2004 Mar 19.

Abstract

We sought to determine whether the fa (leptin receptor) mutation was a major determinant of the putative obesity effects on respiratory frequency in an intercross between the Brown Norway (low breathing frequency, nonobese strain) and the Zucker (moderately high breathing frequency, with the fa mutation) strains. The hypothesis was that rats bearing one (heterozygote) or two (homozygote) alleles of the Glu296Pro point mutation (fa) would have a uniformly high respiratory frequency in the second filial (F2) generation, compared with wild-type animals. In addition to breathing frequency, tidal volume and minute ventilation were assessed during baseline, acute hypoxic (10% O2-0% CO2-balance nitrogen), hypercapnic (93% O2-7% CO2), hyperoxic (100% O2-0% CO2), and combined (10% O2-3% CO2-balance nitrogen) challenges in fa homozygote (fa/fa; n = 24), fa heterozygote (fa/wt; n = 33), and wild-type (wt/wt; n = 19) animals. Phenotypes were adjusted with stepwise regression analyses for the effects of age, sex, length, and litter size. Broad-sense heritability was estimated by examining the variance of the traits in first filial and F2 generations. ANOVAs were used to determine the mode of inheritance of the fa allele in the F2 generation. As anticipated, weight demonstrated the greatest overall broad-sense heritability (77%) and was the result of the recessive mutation. Breathing parameters during the hypoxic, hypercapnic, and combined challenges demonstrated a wide range of heritability from 5 to 96%, with a very nonuniform proportion of heritability explained by the leptin receptor. At best, for frequency 4.5 min into the hypercapnic hypoxic challenge, approximately 20% of the total heritability (approximately 67%) could be attributed to an effect of the leptin receptor mutation. We conclude that, unlike its major effect on weight, the effect of the fa allele is not a major gene involved in the regulation of breathing frequency.

摘要

我们试图确定在棕色挪威大鼠(低呼吸频率,非肥胖品系)和 Zucker 大鼠(中等高呼吸频率,携带 fa 突变)品系的杂交后代中,fa(瘦素受体)突变是否是假定的肥胖对呼吸频率影响的主要决定因素。假设是,携带 Glu296Pro 点突变(fa)一个等位基因(杂合子)或两个等位基因(纯合子)的大鼠在第二代(F2)中与野生型动物相比将具有一致的高呼吸频率。除了呼吸频率外,还在基线、急性低氧(10% O2 - 0% CO2 - 平衡氮气)、高碳酸血症(93% O2 - 7% CO2)、高氧(100% O2 - 0% CO2)以及联合(10% O2 - 3% CO2 - 平衡氮气)刺激条件下评估了 fa 纯合子(fa/fa;n = 24)、fa 杂合子(fa/wt;n = 33)和野生型(wt/wt;n = 19)动物的潮气量和分钟通气量。通过逐步回归分析对年龄、性别、体长和窝仔数的影响来调整表型。通过检查第一代和 F2 代性状的方差来估计广义遗传力。使用方差分析来确定 F2 代中 fa 等位基因的遗传模式。如预期的那样,体重表现出最大的总体广义遗传力(77%),并且是隐性突变的结果。在低氧、高碳酸血症和联合刺激期间的呼吸参数表现出 5%至 96%的广泛遗传力范围,瘦素受体解释的遗传力比例非常不均匀。在高碳酸血症低氧刺激 4.5 分钟时的频率方面,最多约 20%的总遗传力(约 67%)可归因于瘦素受体突变的影响。我们得出结论,与它对体重的主要影响不同,fa 等位基因的影响不是参与呼吸频率调节的主要基因。

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