首页> 外文期刊>American Journal of Physiology >Renal function of gene-targeted mice lacking both SGK1 and SGK3.
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Renal function of gene-targeted mice lacking both SGK1 and SGK3.

机译:缺少SGK1和SGK3的基因靶向小鼠的肾功能。

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摘要

Serum- and glucocorticoid-inducible kinase (SGK) 1 and SGK3 share the ability to upregulate several ion channels, including the epithelial Na(+) channel. Whereas SGK1 is under genomic control of mineralocorticoids and glucocorticoids, SGK3 is constitutively expressed. The SKG1-knockout (sgk1(-/-)) mouse is seemingly normal when it is fed a standard diet, but its ability to retain NaCl is impaired when it is fed a salt-deficient diet. In the SGK3-knockout (sgk3(-/-)) mouse fed standard and salt-deficient diets, hair growth is strikingly delayed but NaCl excretion is normal. Thus the possibility was considered that SGK1 and SGK3 could mutually replace each other, thus preventing severe NaCl loss in sgk1(-/-) and sgk3(-/-) mice. We crossed SGK1- and SGK3-knockout mice and compared renal electrolyte excretion of the double mutants (sgk1(-/-)/sgk3(-/-)) with that of their wild-type littermates (sgk1(+/+)/sgk3(+/+)). Similar to sgk3(-/-) mice, the sgk1(-/-)/sgk3(-/-) mice display delayed hair growth. Blood pressure was slightly, but significantly (P < 0.03), lower in sgk1(-/-)/sgk3(-/-) (102 +/- 4 mmHg) than in sgk1(+/+)/sgk3(+/+) (114 +/- 3 mmHg) mice, a difference that was maintained in mice fed low- and high-salt diets. Plasma aldosterone concentrations were significantly (P < 0.01) higher in sgk1(-/-)/sgk3(-/-) than in sgk1(+/+)sgk3(+/+) mice fed control (511 +/- 143 vs. 143 +/- 32 pg/ml) and low-salt (1,325 +/- 199 vs. 362 +/- 145 pg/ml) diets. During salt depletion, absolute and fractional excretions of Na(+) were significantly (P < 0.01) higher in sgk1(-/-)/sgk3(-/-) (1.2 +/- 0.2 micromol/24 h g body wt, 0.12 +/- 0.03%) than in sgk1(+/+)/sgk3(+/+) (0.4 +/- 0.1 micromol/24 h g body wt, 0.04 +/- 0.01%) mice. The sgk1(-/-)/sgk3(-/-) mice share the delayed hair growth with sgk3(-/-) mice and the modestly impaired renal salt retention with sgk1(-/-) mice. Additional lack of the isoform kinase does not substantially compound the phenotype for either property.
机译:血清和糖皮质激素诱导激酶(SGK)1和SGK3具有上调几个离子通道(包括上皮Na(+)通道)的能力。 SGK1受盐皮质激素和糖皮质激素的基因组控制,而SGK3组成型表达。当喂食标准饮食时,SKG1-敲除(sgk1(-/-))小鼠看似正常,但喂食缺盐饮食时,其保留NaCl的能力受损。在SGK3基因敲除(sgk3(-/-))小鼠饲喂的标准饮食和缺盐饮食中,毛发生长显着延迟,但NaCl排泄是正常的。因此,认为SGK1和SGK3可以相互替换,从而防止了sgk1(-/-)和sgk3(-/-)小鼠中NaCl的严重损失。我们杂交了SGK1和SGK3基因敲除小鼠,比较了双突变体(sgk1(-/-)/ sgk3(-/-))与野生同窝仔动物(sgk1(+ / +)/ sgk3)的肾脏电解质排泄(+ / +))。与sgk3(-/-)小鼠类似,sgk1(-/-)/ sgk3(-/-)小鼠显示出延迟的头发生长。 sgk1(-/-)/ sgk3(-/-)(102 +/- 4 mmHg)的血压略低于sgk1(+ / +)/ sgk3(+ / +),但显着(P <0.03) (114 +/- 3 mmHg)小鼠,用低盐和高盐饮食喂养的小鼠保持这种差异。 sgk1(-/-)/ sgk3(-/-)的血浆醛固酮浓度显着高于对照组的sgk1(+ / +)sgk3(+ / +)小鼠(511 +/- 143 vs. 143 +/- 32 pg / ml)和低盐(1325 +/- 199 vs.362 +/- 145 pg / ml)饮食。在盐耗竭过程中,sgk1(-/-)/ sgk3(-/-)(1.2 +/- 0.2 micromol / 24 hg体重,0.12 +)中Na(+)的绝对排泄和分数排泄显着(P <0.01) +/- 0.03%)(比sgk1(+ / +)/ sgk3(+ / +)(0.4 +/- 0.1 micromol / 24 hg体重,0.04 +/- 0.01%)小鼠高。 sgk1(-/-)/ sgk3(-/-)小鼠与sgk3(-/-)小鼠共享延迟的毛发生长,而sgk1(-/-)小鼠具有适度受损的肾盐滞留性。缺少同种型激酶实质上不能使这两种特性的表型复合。

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