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Absence of a losartan interaction with renal lithium excretion in the rat

机译:大鼠体内缺少氯沙坦与肾锂排泄的相互作用

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1 The interaction of losartan, a non-peptide specific AT_1 receptor antagonist with the renal handling of lithium was analysed in conscious normotensive Wistar rats and compared with the known increase in renal tubular lithium reabsorption induced by the non-steroidal anti-inflammatory drug, indomethacin. 2 The rats were treated for five days with losartan (10 mg kg~(-1) day~(-1), orally), indomethacin (2.5 mg kg~(-1) day~(-1), intramuscularly) or their solvents. Lithium chloride (16.7 mg kg~(-1), i.p.) was given as a single dose on the fifth day; renal functions were then measured. 3 Indomethacin, in the absence of any effect on creatinine clearance, increased renal fractional lithium reabsorption and led to an increase in plasma lithium levels. 4 Losartan did not modify renal lithium handling and its plasma level. No change was observed in renal lithium clearance, the quantity of filtered lithium or the fractional reabsorption of the metal. As expected, losartan had no effect on systolic blood pressure in normotensive rats. 5 In conclusion, our results indicate that losartan, when given orally in the rat at a dose of 10 mg kg~(-1) day~(-1) over five days, does not modify renal lithium handling. They suggest that blockade of the angiotensin Ⅱ receptors does not interfere with renal lithium reabsorption, which occurs mainly at a proximal tubular site.
机译:1在有意识的血压正常的Wistar大鼠中分析了非肽特异性AT_1受体拮抗剂洛沙坦与肾脏对锂的相互作用,并与已知的由非甾体类抗炎药吲哚美辛引起的肾小管锂重吸收的增加进行了比较。 。 2用氯沙坦(10 mg kg〜(-1)天〜(-1),口服),消炎痛(2.5 mg kg〜(-1)天〜(-1),肌肉内)或其大鼠治疗五天。溶剂。在第五天以单剂量给予氯化锂(16.7 mg kg〜(-1),腹膜内)。然后测量肾功能。 3消炎痛对肌酐清除率没有任何影响,但会增加肾脏对锂的重吸收分数,并导致血浆锂水平升高。 4 Losartan并未改变肾锂的处理及其血浆水平。肾锂清除率,锂的过滤量或金属的部分重吸收均未观察到变化。如预期的那样,氯沙坦对血压正常的大鼠的收缩压没有影响。 5总之,我们的结果表明,氯沙坦在大鼠中以10 mg kg〜(-1)天〜(-1)的剂量在五天内口服给药时,不会改变肾锂的处理。他们认为,血管紧张素Ⅱ受体的阻滞不干扰肾锂的重吸收,肾重吸收主要发生在肾小管近端。

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