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证据表明,雌激素对肾脏磷酸盐处理和钠依赖性磷酸盐协同转运蛋白 IIa 表达具有甲状旁腺激素非依赖性的慢性作用。

Evidence of a parathyroid hormone-independent chronic effect of estrogen on renal phosphate handling and sodium-dependent phosphate cotransporter type IIa expression.

机构信息

Department of Medicine, Hadassah University Medical Center, The Hebrew University Hadassah Medical School, Jerusalem, Israel.

出版信息

Horm Metab Res. 2010 Apr;42(4):230-6. doi: 10.1055/s-0029-1246182. Epub 2010 Jan 29.

Abstract

The effects of estrogen on phosphate metabolism are not well understood. To better define the chronic effects of estrogen on phosphate balance and on renal phosphate handling, the following groups were examined: A. young male and female rats, age- and weight-matched (age 8-10 weeks, 1 (st) study), and B. ovariectomized female rats (OVX), 22 weeks old, ovariectomized aged-matched rats receiving estrogen replacement (15 micromol x 3/week) for 14 weeks (OVX+E), control female rats (intact ovaries), and male rats, both age matched to OVX and OVX+E (2 (nd) Study). In younger females (1 (st) study), plasma phosphate was lower, whereas the urinary excretion of phosphate was higher than in males. In adult intact females and in OVX+E urinary excretion of phosphate was higher than in males and OVX (2 (nd) Study). In these rats, a significant correlation between plasma phosphate and estrogen level was found. Sodium-dependent phosphate cotransporter (NaPiIIa) mRNA expression and protein abundance were higher in the renal cortex of younger male rats than in age- and weight-matched females. In adult rats, NaPiIIa mRNA and protein abundance were higher in OVX than in OVX+E, and in mature males as compared with age-matched females. These differences were not related to the parathyroid hormone (PTH) levels. Chronic estrogen administration was also associated with increased plasma calcium level and urinary calcium excretion. These results suggest that chronic estrogen treatment is associated with an inhibitory, PTH-independent effect on the expression of NaPiIIa in the kidney, leading to sex-related differences in phosphate balance.

摘要

雌激素对磷酸盐代谢的影响尚不清楚。为了更好地定义雌激素对磷酸盐平衡和肾脏磷酸盐处理的慢性影响,检查了以下组:A. 年轻的雄性和雌性大鼠,年龄和体重匹配(年龄 8-10 周,第 1 项研究),和 B. 去卵巢雌性大鼠(OVX),22 周龄,接受 14 周雌激素替代治疗的去卵巢年龄匹配大鼠(15 微摩尔 x 3/周)(OVX+E),对照雌性大鼠(完整卵巢)和雄性大鼠,年龄均与 OVX 和 OVX+E 匹配(第 2 项研究)。在年轻女性中(第 1 项研究),血浆磷酸盐较低,而磷酸盐的尿排泄量高于男性。在成年雌性和 OVX+E 中,磷酸盐的尿排泄量高于雄性和 OVX(第 2 项研究)。在这些大鼠中,发现血浆磷酸盐与雌激素水平之间存在显著相关性。年轻雄性大鼠肾脏皮质中的钠依赖性磷酸盐共转运蛋白(NaPiIIa)mRNA 表达和蛋白丰度高于年龄和体重匹配的雌性大鼠。在成年大鼠中,NaPiIIa mRNA 和蛋白丰度在 OVX 中高于 OVX+E,在成熟雄性中高于年龄匹配的雌性。这些差异与甲状旁腺激素(PTH)水平无关。慢性雌激素治疗还与血浆钙水平升高和尿钙排泄增加有关。这些结果表明,慢性雌激素治疗与肾脏中 NaPiIIa 的表达呈抑制性、PTH 无关,导致性别相关的磷酸盐平衡差异。

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