Involvement of γ-Glutamyl Transpeptidase in Ischemia/Reperfusion-Induced Cardiac Dysfunction in Isolated Rat Hearts

被引:4
作者
Koyama, Takeshi [1 ]
Tsubota, Akari [1 ]
Sawano, Tatsuya [1 ,2 ]
Tawa, Masashi [1 ,3 ]
Watanabe, Bunta [4 ]
Hiratake, Jun [4 ]
Nakagawa, Keisuke [1 ]
Matsumura, Yasuo [1 ]
Ohkite, Mamoru [1 ]
机构
[1] Osaka Univ Pharmaceut Sci, Lab Pathol & Mol Pharmacol, 4-20-1 Nasahara, Takatsuki, Osaka 5691094, Japan
[2] Tottori Univ, Div Pharmacol, Fac Med, 86 Nishi Cho, Yonago, Tottori 6838503, Japan
[3] Kanazawa Med Univ, Dept Pharmacol, 1-1 Daigaku, Kahoku, Ishikawa 9200293, Japan
[4] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
关键词
gamma-glutamyl transpeptidase; GGsTop; ischemia-reperfusion; cardiac dysfunction; superoxide; ISCHEMIA-REPERFUSION INJURY; LIPID-PEROXIDATION; TRANSFERASE TRANSPEPTIDASE; VENTRICULAR-FUNCTION; GLUTATHIONE; INHIBITOR; INFARCTION; GGSTOP; MALONDIALDEHYDE; METABOLISM;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
GGsTop is a highly potent and specific, and irreversible gamma-glutamyl transpeptidase (GGT) inhibitor without any influence on glutamine amidotransferases. The aim of the present study was to investigate the involvement of GGT in ischemia/reperfusion-induced cardiac dysfunction by assessing the effects of a treatment with GGsTop. Using a Langendorff apparatus, excised rat hearts underwent 40 min of global ischemia without irrigation and then 30 min of reperfusion. GGT activity was markedly increased in cardiac tissues exposed to ischemia, and was inhibited by the treatment with GGsTop. Exacerbation of cardiac functional parameters caused by ischemia and reperfusion, namely the reduction of left ventricular (LV) developed pressure and the maximum and negative minimum values of the first derivative of LV pressure, and the increment in LV end-diastolic pressure was significantly attenuated by GGsTop treatment. The treatment with GGsTop suppressed excessive norepinephrine release in the coronary perfusate, a marker for myocardial dysfunction, after ischemia/reperfusion. In addition, oxidative stress indicators in myocardium, including superoxide and malondialdehyde, after ischemia/reperfusion were significantly low in the presence of GGsTop. These observations demonstrate that enhanced GGT activity contributes to cardiac damage after myocardial ischemia/reperfusion, possibly via increased oxidative stress and subsequent norepinephrine overflow. GGT inhibitors have potential as a therapeutic strategy to prevent myocardial ischemia/reperfusion injury in vivo.
引用
收藏
页码:1947 / 1952
页数:6
相关论文
共 33 条
  • [1] ALLISON RD, 1985, METHOD ENZYMOL, V113, P419
  • [2] Plasma membrane glutathione transporters and their roles in cell physiology and pathophysiology
    Ballatori, Nazzareno
    Krance, Suzanne M.
    Marchan, Rosemarie
    Hammond, Christine L.
    [J]. MOLECULAR ASPECTS OF MEDICINE, 2009, 30 (1-2) : 13 - 28
  • [3] Dhalla NS, 1999, CAN J CARDIOL, V15, P587
  • [4] Prooxidant reactions promoted by soluble and cell-bound γ-glutamyltransferase activity
    Dominici, S
    Paolicchi, A
    Corti, A
    Maellaro, E
    Pompella, A
    [J]. GLUTHIONE TRANSFERASES AND GAMMA-GLUTAMYL TRANSPEPTIDASES, 2005, 401 : 484 - 501
  • [5] OXYGEN-MEDIATED MYOCARDIAL DAMAGE DURING ISCHEMIA AND REPERFUSION - ROLE OF THE CELLULAR DEFENSES AGAINST OXYGEN-TOXICITY
    FERRARI, R
    CECONI, C
    CURELLO, S
    GUARNIERI, C
    CALDARERA, CM
    ALBERTINI, A
    VISIOLI, O
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1985, 17 (10) : 937 - 945
  • [6] Design, synthesis, and evaluation of γ-phosphono diester analogues of glutamate as highly potent inhibitors and active site probes of γ-glutamyl transpeptidase
    Han, Liyou
    Hiratake, Jun
    Kamiyama, Akane
    Sakata, Kanzo
    [J]. BIOCHEMISTRY, 2007, 46 (05) : 1432 - 1447
  • [7] HERMAN RP, 1988, BIOMED BIOCHIM ACTA, V47, pS174
  • [8] MALONDIALDEHYDE AND GLUTATHIONE PRODUCTION IN ISOLATED-PERFUSED HUMAN AND RAT HEARTS
    JANSSEN, M
    KOSTER, JF
    BOS, E
    DEJONG, JW
    [J]. CIRCULATION RESEARCH, 1993, 73 (04) : 681 - 688
  • [9] Jiang SY, 2013, EXP CLIN CARDIOL, V18, P53
  • [10] Phosphonate-based irreversible inhibitors of human γ-glutamyl transpeptidase (GGT). GGsTop is a non-toxic and highly selective inhibitor with critical electrostatic interaction with an active-site residue Lys562 for enhanced inhibitory activity
    Kamiyama, Akane
    Nakajima, Mado
    Han, Liyou
    Wada, Kei
    Mizutani, Masaharu
    Tabuchi, Yukiko
    Kojima-Yuasa, Akiko
    Matsui-Yuasa, Isao
    Suzuki, Hideyuki
    Fukuyama, Keiichi
    Watanabe, Bunta
    Hiratake, Jun
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2016, 24 (21) : 5340 - 5352