Department of Applied Mathematics, University of Waterloo, Waterloo, Ontario, Canada.
Cheriton School of Computer Science, University of Waterloo, Waterloo, Ontario, Canada.
Am J Physiol Renal Physiol. 2023 Mar 1;324(3):F274-F286. doi: 10.1152/ajprenal.00296.2022. Epub 2023 Jan 26.
Sex differences in renal function and blood pressure have been widely described across many species. Blood pressure dips during sleep and peaks in the early morning. Similarly, glomerular filtration rate, filtered electrolyte loads, urine volume, and urinary excretion all exhibit notable diurnal rhythms, which reflect, in part, the regulation of renal transporter proteins by circadian clock genes. That regulation is sexually dimorphic; as such, sex and time of day are not two independent regulators of kidney function and blood pressure. The objective of the present study was to assess the effect of sex and administration time on the natriuretic and diuretic effects of loop, thiazide, and K-sparing diuretics, which are common treatments for hypertension. Loop diuretics inhibit Na-K-2Cl cotransporters on the apical membrane of the thick ascending limb, thiazide diuretics inhibit Na-Cl cotransporters on the distal convoluted tubule, and K-sparing diuretics inhibit epithelial Na channels on the connecting tubule and collecting duct. We simulated Na transporter inhibition using sex- and time-of-day-specific computational models of mouse kidney function. The simulation results highlighted significant sex and time-of-day differences in the drug response. Loop diuretics induced larger natriuretic and diuretic effects during the active phase. The natriuretic and diuretic effects of thiazide diuretics exhibited sex and time-of-day differences, whereas these effects of K-sparing diuretics exhibited a significant time-of-day difference in females only. The kaliuretic effect depended on the type of diuretics and time of administration. The present computational models can be a useful tool in chronotherapy, to tailor drug administration time to match the body's diurnal rhythms to optimize the drug effect. Sex influences cardiovascular disease, and the timing of onset of acute cardiovascular events exhibits circadian rhythms. Kidney function also exhibits sex differences and circadian rhythms. How do the natriuretic and diuretic effects of diuretics, a common treatment for hypertension that targets the kidneys, differ between the sexes? And how do these effects vary during the day? To answer these questions, we conducted computer simulations to assess the effects of loop, thiazide, and K-sparing diuretics.
性别在许多物种的肾功能和血压中都存在差异。血压在睡眠期间下降,清晨时达到峰值。同样,肾小球滤过率、过滤的电解质负荷、尿量和尿排泄都表现出明显的昼夜节律,部分反映了肾脏转运蛋白受昼夜节律基因的调节。这种调节具有性别二态性;因此,性别和一天中的时间不是肾脏功能和血压的两个独立调节因素。本研究的目的是评估性别和给药时间对常用高血压治疗药物——袢利尿剂、噻嗪类利尿剂和保钾利尿剂的利钠和利尿作用的影响。袢利尿剂抑制升支粗段顶端膜上的 Na-K-2Cl 共转运体,噻嗪类利尿剂抑制远曲小管上的 Na-Cl 共转运体,保钾利尿剂抑制连接小管和收集管上的上皮 Na 通道。我们使用基于性别的小鼠肾脏功能的计算模型模拟了 Na 转运体的抑制作用。模拟结果突出了药物反应中的显著性别和时间差异。袢利尿剂在活动期产生更大的利钠和利尿作用。噻嗪类利尿剂的利钠和利尿作用存在性别和时间差异,而保钾利尿剂的这些作用仅在雌性动物中存在时间差异。排钾作用取决于利尿剂的类型和给药时间。本研究中的计算模型可作为时间治疗的有用工具,通过调整药物给药时间以适应身体的昼夜节律,从而优化药物效果。性别影响心血管疾病,急性心血管事件的发作时间呈现昼夜节律。肾功能也存在性别差异和昼夜节律。作为治疗高血压的常用药物,利尿剂对肾脏的利钠和利尿作用在两性之间有何差异?这些作用在一天中如何变化?为了回答这些问题,我们进行了计算机模拟以评估袢利尿剂、噻嗪类利尿剂和保钾利尿剂的作用。