摘要
Tenapanor是一种新型降磷药物,主要作用于钠/氢交换蛋白3(NHE3)起抑制作用,此外还可以通过下调磷酸钠盐协同转运蛋白(NAPI)的表达,从而降低肠道对磷的吸收。Tenapanor主要用于治疗终末期肾脏病-血液透析(ESRDHD)患者高磷血症。腹泻为本品最常见的不良反应。本文通过对Tenapanor进行文献检索,就其药理作用、药动学特性、临床评价、安全性、药物相互作用和用法用量进行综述。
Tenapanor is a novel phosphorus-low-ering drug,which mainly inhibits sodium/hydrogen exchange protein 3(NHE3),and also reduces intes-tinal phosphorus absorption by down-regulating the expression of sodium phosphate co-transporter protein(NAPI).Tenapanor is mainly used for the treatment of hyperphosphatemia in patients with end-stage renal disease-hemodialysis(ESRD-HD).Diarrhea is the most common adverse reaction to this product.This article reviews Tenapanor by per-forming a literature search on its pharmacological effects,pharmacokinetic properties,clinical evalua-tion,safety,drug interactions and dosage.
作者
侯文平
徐磊
苏长海
HOU Wenping;XU Lei;SU Changhai(Graduate School of Baotou Medical College,Baotou 014060,Inner Mongolia,China;Department of Pharmacy,Ordos Central Hospital,Ordos 017000,Inner Mongolia,China)
出处
《中国临床药理学与治疗学》
CAS
CSCD
2023年第12期1429-1435,共7页
Chinese Journal of Clinical Pharmacology and Therapeutics
基金
鄂尔多斯市医学重点学科建设资助(鄂卫健发【2020】230号)
医院药物警戒研究协作组医院药学科研专项课题(DRM2022019)。