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Renal electrolyte and fluid handling in the rat following chloroquine and/or ethanol administration.

机译:服用氯喹和/或乙醇后大鼠的肾脏电解质和液体处理。

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We postulated that chloroquine and/or ethanol affect plasma arginine vasopressin (AVP) concentrations to alter renal function. Therefore, we studied the effects of chloroquine and/or ethanol on plasma AVP concentrations and fluid, urinary Na(+) and K(+) outputs in separate groups of anaesthetized Sprague-Dawley (SD) rats challenged with a continuous jugular infusion of 0.077 M NaCl at 150 microl.min(-1). After a 3-h equilibration period, vehicle, chloroquine (0.06 microg. min(-1)), ethanol (2.4 or 24 microg.min(-1)) or both chloroquine and ethanol were added to the infusate after 1 h (control) for 1 h 20 min (treatment). The animals were switched back to the infusate alone for the final 1 h 40 min recovery periods. Urine flow Na(+) and K(+) excretion rates were determined at 20-min intervals over the subsequent 4-h postequilibration period. Blood was collected from separate groups of animals at the end of treatment period or equivalent time for control animals for measurement of plasma aldosterone and AVP concentrations by radioimmunoassay. Simultaneous chloroquine and ethanol infusion significantly (p < 0.01) increased plasma chloroquine concentrations in an ethanol dose-dependent manner by comparison with animals administered chloroquine alone. Chloroquine infusion alone (0.06 microg.min(-1)) and/or ethanol (2.4 or 24 microg.min(-1)) elevated plasma AVP concentrations from 9.73 +/- 1.64 fmol.l(-1) in control rats to 15.65 +/- 2.49 fmol.l(-1), 17. 39 +/- 4.21 fmol.l(-1), and 33.87 +/- 6.18 fmol.l(-1), respectively. Separate administration of chloroquine or ethanol at low dose rates increased urinary Na(+) excretion rates. We conclude that the impairment of renal electrolyte handling associated with chloroquine administration may be exacerbated by ethanol.
机译:我们推测氯喹和/或乙醇会影响血浆精氨酸加压素(AVP)的浓度,从而改变肾功能。因此,我们研究了在接受连续颈静脉输注0.077的麻醉的Sprague-Dawley(SD)大鼠的不同组中,氯喹和/或乙醇对血浆AVP浓度和液体,尿Na(+)和K(+)输出的影响。 M NaCl浓度为150 microl.min(-1)。平衡3小时后,将溶媒,氯喹(0.06 microg.min(-1)),乙醇(2.4或24 microg.min(-1))或氯喹和乙醇都添加到1h后的输注液中(对照)1 h 20分钟(处理)。在最后的1小时40分钟恢复期,将动物单独换回输注液。在随后的4小时平衡后的20分钟内确定尿液Na(+)和K(+)的排泄率。在治疗期结束时或与对照组动物等效的时间从不同的动物组中收集血液,以通过放射免疫测定法测量血浆醛固酮和AVP浓度。与单独施用氯喹的动物相比,同时氯喹和乙醇输注显着(p <0.01)以乙醇剂量依赖性方式增加了血浆氯喹浓度。在对照大鼠中,单独的氯喹输注(0.06 microg.min(-1))和/或乙醇(2.4或24 microg.min(-1))使血浆AVP浓度从9.73 +/- 1.64 fmol.l(-1)增加到15.65 +/- 2.49 fmol.l(-1),17。39 +/- 4.21 fmol.l(-1)和33.87 +/- 6.18 fmol.l(-1)。低剂量率的氯喹或乙醇的单独给药增加了尿Na(+)的排泄率。我们得出结论,乙醇可能加剧与氯喹给药有关的肾电解质处理能力的损害。

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