Manifestation of Multidrug Resistance Protein 3 (MRP3) in Liver and Kidney Cells in Cholestasis: Effects of Hyperprolactinemia

被引:0
|
作者
M. I. Aleksandrova
N. S. Kushnareva
O. V. Smirnova
机构
[1] M. V. Lomonosov Moscow State University,Laboratory of Endocrinology, Biological Faculty
关键词
multidrug resistance protein 3 (mrp3); hyperprolactinemia; cholestasis; liver; kidney;
D O I
暂无
中图分类号
学科分类号
摘要
Immunohistochemistry with semiquantitative image analysis showed that cholestasis induced an increase in the manifestation of mrp3 in cholangiocytes of female rats, but did not affect this parameter in the studied structures of kidney. Under conditions of normal liver function, mrp3 expression in cholangiocytes was also elevated during hyperprolactinemia. Expression of mrp3 in cholangiocytes directly correlated with prolactin receptor expression. In cholestasis, prolactin increased mrp3 manifestation of only in the distal renal tubules. Thus, mrp3 manifestation increases in liver cells, but remains unchanged in kidney cells. The hyperprolactinemia-induced changes in the mrp3 levels and their correlations with prolactin receptor expression were shown to differ in the kidney and liver cells. It was hypothesized that prolactin produced a direct effect on mrp3 expression in cholangiocytes.
引用
收藏
页码:508 / 511
页数:3
相关论文
共 50 条
  • [41] The molecular and immunohistochemical expression of multidrug resistance-associated protein (MRP) 3 in the liver and intestine of patients with cholestasis and its biological significance.
    Shoda, J
    Oda, K
    Kamiya, J
    Nimura, Y
    Suzuki, H
    Sugiyama, Y
    Miyazaki, H
    Kawamoto, T
    Tanaka, N
    GASTROENTEROLOGY, 2000, 118 (04) : A933 - A933
  • [42] Characterization of inducible nature of MRP3 in rat liver
    Ogawa, K
    Suzuki, H
    Hirohashi, T
    Ishikawa, T
    Meier, PJ
    Hirose, K
    Akizawa, T
    Yoshioka, M
    Sugiyama, Y
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 278 (03): : G438 - G446
  • [43] Functional Characterization of Multidrug Resistance-Associated Protein 3 (Mrp3/Abcc3) in the Basolateral Efflux of Glucuronide Conjugates in the Mouse Small Intestine
    Kitamura, Yoshiaki
    Kusuhara, Hiroyuki
    Sugiyama, Yuichi
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2010, 332 (02): : 659 - 666
  • [44] Transport activity of human MRP3 expressed in Sf9 cells: Comparative studies with rat MRP3
    Akita, H
    Suzuki, H
    Hirohashi, T
    Takikawa, H
    Sugiyama, Y
    PHARMACEUTICAL RESEARCH, 2002, 19 (01) : 34 - 41
  • [45] Expression of multidrug resistance associated genes MRP1, MRP2 and MRP3 in primary and anthracycline exposed breast cancer
    Faneyte, I. F.
    Kristel, P. M. P.
    van de Vijver, M. J.
    EJC SUPPLEMENTS, 2004, 2 (03): : 106 - 107
  • [46] Transport Activity of Human MRP3 Expressed in Sf9 Cells: Comparative Studies with Rat MRP3
    Hidetaka Akita
    Hiroshi Suzuki
    Tomoko Hirohashi
    Hajime Takikawa
    Yuichi Sugiyama
    Pharmaceutical Research, 2002, 19 : 34 - 41
  • [47] Major glucuronide metabolites of testosterone are primarily transported by MRP2 and MRP3 in human liver, intestine and kidney
    Li, Cindy Yanfei
    Basit, Abdul
    Gupta, Anshul
    Gaborik, Zsuzsanna
    Kis, Emese
    Prasad, Bhagwat
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2019, 191
  • [48] Ethynylestradiol increases expression and activity of rat liver MRP3
    Ruiz, Maria L.
    Villanueva, Silvina S. M.
    Luquita, Marcelo G.
    Vore, Mary
    Mottino, Aldo D.
    Catania, Viviana A.
    DRUG METABOLISM AND DISPOSITION, 2006, 34 (06) : 1030 - 1034
  • [49] Limited modulation of the transport activity of the human multidrug resistance proteins MRP1, MRP2 and MRP3 by nicotine glucuronide metabolites
    Létourneau, IJ
    Bowers, RJ
    Deeley, RG
    Cole, SPC
    TOXICOLOGY LETTERS, 2005, 157 (01) : 9 - 19
  • [50] MRP3 As a Novel Resistance Factor for Sorafenib in Hepatocellular Carcinoma
    Tomonari, Tetsu
    Takeishi, Shunsaku
    Taniguchi, Tatsuya
    Tanaka, Takahiro
    Tanaka, Hironori
    Kimura, Tetsuo
    Okamoto, Koichi
    Miyamoto, Hiroshi
    Muguruma, Naoki
    Takayama, Tetsuji
    GASTROENTEROLOGY, 2016, 150 (04) : S514 - S514