Department of Internal Medicine, C. Hospitalar Universitario S. João, Porto, Portugal.
Assistance Publique Hôpitaux de Paris, Georges Pompidou European Hospital, Centre d'Investigation Clinique, Paris.
J Hypertens. 2019 Nov;37(11):2225-2231. doi: 10.1097/HJH.0000000000002150.
P-glycoprotein (P-gp), the product of the ABCB1 gene, is involved in the transport of aldosterone and cortisol in adrenal cells in vitro but its physiological role in humans remains controversial. Our objective was to test the influence of P-gp polymorphisms on aldosterone.
We evaluated plasma aldosterone concentration (PAC), urinary aldosterone, and blood pressure in a cohort of white normotensive men at baseline on diets unrestricted for sodium and potassium and after a 5-day treatment with 500 mg b.i.d. clarithromycin, a P-gp inhibitor. Included were 20 homozygous wild-type (P-gp0), 20 heterozygous (P-gp1), and 20 individuals with combined 2677G>T/A-3435C>T loss-of-function polymorphism of the ABCB1 gene (P-gp2).
At baseline, PAC, urinary aldosterone, urinary free cortisol to urine creatinine ratios, and blood pressure did not differ in the three genotypes. After clarithromycin administration, the urinary aldosterone to creatinine ratio increased by an average of 30% in the entire cohort (P < 0.001, n = 60). Increases were pronounced in P-gp1 (+40%; P = 0.014) and P-gp2 individuals (+50%; P = 0.020) but lesser and were NS in P-gp0 individuals (+10%; P = 0.259). PAC also increased from baseline after clarithromycin treatment in all individuals (+19%, P = 0.050); however, the increase in PAC was NS when the three genotypes were analyzed separately.
In our experimental conditions, the interaction between P-gp inhibition and the ABCB1 genotype, suggests that aldosterone is indeed a physiological endogenous substrate of P-gp in humans and that P-gp interferes with the net equilibrium between aldosterone secretion and elimination processes in humans.Clinical Trial Registration - URL: http://www.clinicaltrials.gov. Unique identifier: NCT01627665.
P-糖蛋白(P-gp)是 ABCB1 基因的产物,它参与体外肾上腺细胞中醛固酮和皮质醇的转运,但它在人类中的生理作用仍存在争议。我们的目的是检测 P-gp 多态性对醛固酮的影响。
我们在一组白人正常血压男性中评估了基础饮食不受钠和钾限制以及 5 天 500mg bid 克拉霉素治疗后的血浆醛固酮浓度(PAC)、尿醛固酮和血压。包括 20 名纯合野生型(P-gp0)、20 名杂合子(P-gp1)和 20 名 ABCB1 基因 2677G>T/A-3435C>T 缺失功能多态性的个体(P-gp2)。
在基线时,三种基因型的 PAC、尿醛固酮、尿游离皮质醇与尿肌酐比值和血压均无差异。克拉霉素给药后,整个队列的尿醛固酮与肌酐比值平均增加 30%(P<0.001,n=60)。在 P-gp1(+40%;P=0.014)和 P-gp2 个体中增加更为显著(+50%;P=0.020),而在 P-gp0 个体中则较少且无统计学意义(+10%;P=0.259)。在所有个体中,PAC 也在克拉霉素治疗后从基线增加(+19%,P=0.050);然而,当单独分析三种基因型时,PAC 的增加无统计学意义。
在我们的实验条件下,P-gp 抑制与 ABCB1 基因型之间的相互作用表明,醛固酮确实是人类 P-gp 的一种生理内源性底物,并且 P-gp 干扰了人类中醛固酮分泌和消除过程之间的净平衡。临床试验注册-网址:http://www.clinicaltrials.gov。唯一标识符:NCT01627665。