In situ hybridization studies of UDP-glucuronosyltransferase UGT1A6 expression in rat testis and brain

被引:17
|
作者
Brands, A [1 ]
Münzel, PA [1 ]
Bock, KW [1 ]
机构
[1] Univ Tubingen, Inst Toxicol, D-72074 Tubingen, Germany
关键词
UDP-glucuronosyltransferase UGT1A6; in situ hybridization; testis; brain;
D O I
10.1016/S0006-2952(00)00274-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
UDP-glucuronosyltransferases (UGTs), in addition to their role in overall pharmacokinetics, play important roles in local protection of cells against toxins and in the control of endogenous receptor ligands. UGT1A6, which conjugates planar phenols, appears to be expressed in many organs, but information on cell-specific expression in these organs is controversial or absent. Therefore, a non-isotopic in situ hybridization method was developed and applied to localize UGT1A6 expression in rat testis and brain. It was found that UGT1A6 is expressed in Sertoli cells and spermatogonia of rat testis and in brain neurons, in particular in hippocampal pyramidal cells and Purkinje cells of the cerebellum. BIOCHEM PHARMACOL 59;11:1441-1444, 2000. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:1441 / 1444
页数:4
相关论文
共 50 条
  • [31] Tissue-specific 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible expression of human UDP-glucuronosyltransferase UGT1A6
    Munzel, PA
    Bookjans, G
    Mehner, G
    Lehmkoster, T
    Bock, KW
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 335 (01) : 205 - 210
  • [32] Effects of β-Naphthoflavone on Ugt1a6 and Ugt1a7 Expression in Rat Brain
    Sakakibara, Yukiko
    Katoh, Miki
    Kondo, Yuya
    Nadai, Masayuki
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2016, 39 (01) : 78 - 83
  • [33] Metabolic Capacity of UDP-glucuronosyltransferase in Rat Brain
    Imai, Kuniyuki
    Katoh, Miki
    Kondo, Yuya
    Nadai, Masayuki
    DRUG METABOLISM REVIEWS, 2010, 42 : 65 - 65
  • [34] Coordinate regulation of UDP-glucuronosyltransferase UGT1A6 induction by 3-methylcholanthrene and multidrug resistance protein MRP2 expression by dexamethasone in primary rat hepatocytes
    Jemnitz, K
    Veres, Z
    Vereczkey, L
    BIOCHEMICAL PHARMACOLOGY, 2002, 63 (12) : 2137 - 2144
  • [35] Comparison of Serotonin Glucuronidation Activity of UDP-glucuronosyltransferase 1a6a (Ugt1a6a) and Ugt1a6b: Evidence for the Preferential Expression of Ugt1a6a in the Mouse Brain
    Uchihashi, Shinsuke
    Nishikawa, Miyu
    Sakaki, Toshiyuki
    Ikushiro, Shin-ichi
    DRUG METABOLISM AND PHARMACOKINETICS, 2013, 28 (03) : 260 - 264
  • [36] Rapid analysis of UDP-glucuronosyltransferase polymorphisms (UGT1A1*28, UGT1A6*2 and UGT1A7*3) using real-time PCR
    Möhrle, B
    Köhle, C
    Bock, KW
    Schwab, M
    Wernet, D
    Münzel, PA
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2002, 365 : R160 - R160
  • [37] Contribution of the Ah receptor to the phenolic antioxidant-mediated expression of human and rat UDP-glucuronosyltransferase UGT1A6 in Caco-2 and rat hepatoma 5L cells
    Münzel, PA
    Schmohl, S
    Buckler, F
    Jaehrling, J
    Raschko, FT
    Köhle, C
    Bock, KW
    BIOCHEMICAL PHARMACOLOGY, 2003, 66 (05) : 841 - 847
  • [38] UDP-glucuronosyltransferase (UGT) activity in sandwich-cultured rat hepatocytes
    Zhang, PJ
    Turncliff, RZ
    Johnson, BM
    Tian, XB
    Brouwer, KLR
    DRUG METABOLISM REVIEWS, 2003, 35 : 56 - 56
  • [39] Glucuronidation of odorant molecules in the rat olfactory system.: Activity, expression and age-linked modifications of UDP-glucuronosyltransferase isoforms, UGT1A6 and UGT2A1, and relation to mitral cell activity
    Leclerc, S
    Heydel, JM
    Amossé, V
    Gradinaru, D
    Cattarelli, M
    Artur, Y
    Goudonnet, H
    Magdalou, J
    Netter, P
    Pelczar, H
    Minn, A
    MOLECULAR BRAIN RESEARCH, 2002, 107 (02): : 201 - 213
  • [40] Expression of UDP-Glucuronosyltransferase 1 (UGT1) and Glucuronidation Activity toward Endogenous Substances in Humanized UGT1 Mouse Brain
    Kutsuno, Yuki
    Hirashima, Rika
    Sakamoto, Masaya
    Ushikubo, Hiroko
    Michimae, Hirofumi
    Itoh, Tomoo
    Tukey, Robert H.
    Fujiwara, Ryoichi
    DRUG METABOLISM AND DISPOSITION, 2015, 43 (07) : 1071 - 1076