Beck N, Yu B P
Am J Physiol. 1982 Aug;243(2):F121-5. doi: 10.1152/ajprenal.1982.243.2.F121.
The effect of aging on urinary concentrating ability and the pathogenic mechanism involved were investigated in Fischer 344 rats. While the rats had free access to drinking water, 24-mo-old rats were polydipsic and polyuric compared with 6- and 12-mo-old rats. The maximum urinary concentrating ability after 40-58 h of water deprivation was not different between 6- and 12-mo-old rats (Uosmol 2,941 +/- 173 vs. 2,706 +/- 96 (SE) mosmol/kg), but it was significantly decreased in 24-mo-old rats (1,885 +/- 172 mosmol/kg, P less than 0.01). Similarly, although 5 mU/ml vasopressin increased the concentration of cAMP and papillary slices in 12-mo-old rats (delta +2.81 +/- 0.62 pmol/mg tissue, P less than 0.01), the same concentration of vasopressin failed to increase the cAMP concentration in 24-mo-old rats (delta +0.25 +/- 0.21 pmol/mg tissue, P greater than 0.05). In the adenylate cyclase preparation of renal papilla, the response to low concentrations of vasopressin was diminished in 24-mo-old rats. The dose-response curve was shifted to the right and the ED50 concentration of vasopressin was increased in 24-mo-old rats compared with 12-mo-old rats: 1.40 +/- 0.12 mU/ml vasopressin vs. 3.04 +/- 0.22. These results suggest that the decrease in vasopressin-dependent cAMP generation may in part be responsible for the impairment of urinary concentrating ability in 24-mo-old rats.
在Fischer 344大鼠中研究了衰老对尿液浓缩能力的影响及其相关致病机制。当大鼠可自由饮水时,与6月龄和12月龄大鼠相比,24月龄大鼠出现多饮多尿。禁水40 - 58小时后的最大尿液浓缩能力在6月龄和12月龄大鼠之间无差异(尿渗透压2,941±173与2,706±96(SE)毫摩尔/千克),但在24月龄大鼠中显著降低(1,885±172毫摩尔/千克,P<0.01)。同样,尽管5 mU/ml血管加压素可增加12月龄大鼠肾乳头切片中cAMP的浓度(增加2.81±0.62皮摩尔/毫克组织,P<0.01),但相同浓度的血管加压素未能增加24月龄大鼠中的cAMP浓度(增加0.25±0.21皮摩尔/毫克组织,P>0.05)。在肾乳头的腺苷酸环化酶制剂中,24月龄大鼠对低浓度血管加压素的反应减弱。与12月龄大鼠相比,24月龄大鼠的剂量 - 反应曲线右移,血管加压素的ED50浓度增加:1.40±0.12 mU/ml血管加压素与3.04±0.22。这些结果表明,血管加压素依赖性cAMP生成的减少可能部分导致了24月龄大鼠尿液浓缩能力的损害。