Jiang Xiaoliang, Zhang Yanrong, Yang Yu, Yang Jian, Asico Laureano D, Chen Wei, Felder Robin A, Armando Ines, Jose Pedro A, Yang Zhiwei
Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences (CAMS) and Comparative Medicine Centre, Peking Union Medical, Beijing, China.
Division of Nephrology, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Am J Physiol Endocrinol Metab. 2017 Jan 1;312(1):E1-E10. doi: 10.1152/ajpendo.00116.2016. Epub 2016 Oct 25.
Gastrin is a peptide hormone that is involved in the regulation of sodium balance and blood pressure. Dopamine, which is also involved in the regulation of sodium balance and blood pressure, directly or indirectly interacts with other blood pressure-regulating hormones, including gastrin. This study aimed to determine the mechanisms of the interaction between gastrin and dopamine and tested the hypothesis that gastrin produced in the kidney increases renal dopamine production to keep blood pressure within the normal range. We show that in human and mouse renal proximal tubule cells (hRPTCs and mRPTCs, respectively), gastrin stimulates renal dopamine production by increasing the cellular uptake of l-DOPA via the l-type amino acid transporter (LAT) at the plasma membrane. The uptake of l-DOPA in RPTCs from C57Bl/6J mice is lower than in RPTCs from normotensive humans. l-DOPA uptake in renal cortical slices is also lower in salt-sensitive C57Bl/6J than in salt-resistant BALB/c mice. The deficient renal cortical uptake of l-DOPA in C57Bl/6J mice may be due to decreased LAT-1 activity that is related to its decreased expression at the plasma membrane, relative to BALB/c mice. We also show that renal-selective silencing of Gast by the renal subcapsular injection of Gast siRNA in BALB/c mice decreases renal dopamine production and increases blood pressure. These results highlight the importance of renal gastrin in stimulating renal dopamine production, which may give a new perspective in the prevention and treatment of hypertension.
胃泌素是一种肽类激素,参与钠平衡和血压的调节。多巴胺也参与钠平衡和血压的调节,它直接或间接与包括胃泌素在内的其他血压调节激素相互作用。本研究旨在确定胃泌素与多巴胺相互作用的机制,并验证肾脏产生的胃泌素会增加肾脏多巴胺生成以将血压维持在正常范围内这一假说。我们发现,在人及小鼠的肾近端小管细胞(分别为hRPTCs和mRPTCs)中,胃泌素通过增加细胞膜上l型氨基酸转运体(LAT)介导的l - 多巴细胞摄取来刺激肾脏多巴胺生成。C57Bl/6J小鼠的肾近端小管细胞对l - 多巴的摄取低于血压正常的人的肾近端小管细胞。盐敏感的C57Bl/6J小鼠肾皮质切片中l - 多巴的摄取也低于盐抵抗的BALB/c小鼠。与BALB/c小鼠相比,C57Bl/6J小鼠肾皮质对l - 多巴摄取不足可能是由于LAT - 1活性降低,这与其在细胞膜上的表达减少有关。我们还发现,在BALB/c小鼠肾被膜下注射胃泌素小干扰RNA(Gast siRNA)对胃泌素进行肾脏选择性沉默会降低肾脏多巴胺生成并升高血压。这些结果突出了肾脏胃泌素在刺激肾脏多巴胺生成中的重要性,这可能为高血压的预防和治疗提供新的视角。