ALTERATIONS OF [H-3] INOSITOL 1,4,5-TRISPHOSPHATE BINDING IN THE POSTISCHEMIC RAT-BRAIN

被引:9
|
作者
NAGASAWA, H
KOGURE, K
机构
[1] Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine, Sendai
关键词
INOSITOL 1,4,5-TRISPHOSPHATE; FOCAL BRAIN ISCHEMIA; POSTISCHEMIC NEURONAL DAMAGE; SECOND MESSENGER SYSTEM;
D O I
10.1016/0304-3940(91)90074-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chronological changes of [H-3]inositol 1,4,5-trisphosphate (IP3) binding sites were determined after 90 min of right middle cerebral artery (MCA) occlusion and after such occlusion followed by different periods of recirculation. One day after the ischemia, [H-3]IP3 binding sites decreased significantly compared with the control values in the lateral segment of the caudate putamen and the cerebral cortex, both supplied by the occluded MCA. Moreover, 3 days after the ischemia, a significant decrease of [H-3]IP3 binding sites was observed in the substantia nigra of ischemic side. In the ipsilateral thalamus, however, there was no alteration until 1 week after the ischemia, and then [H-3]IP3 binding sites increased significantly 2 weeks (P < 0.05) and 4 weeks (P < 0.01) after the ischemia. Based on the present study, we speculate that different mechanisms associated with signal transduction systems may be responsible for exo-focal postischemic delayed neuronal changes in the thalamus and the substantia nigra. The increase of [H-3]IP3 binding sites of the thalamus in the chronic stage may be new evidence of plasticity related to neurotransmission.
引用
收藏
页码:129 / 132
页数:4
相关论文
共 50 条
  • [21] Intrinsic inhibitor of inositol 1,4,5-trisphosphate binding
    Hirata, M
    Yoshida, M
    Kanematsu, T
    Takeuchi, H
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 1999, 190 (1-2) : 179 - 184
  • [22] Structural identification of the myo-inositol 1,4,5-trisphosphate-binding domain in rat brain inositol 1,4,5-trisphosphate 8-kinase
    Togashi, S
    Takazawa, K
    Endo, T
    Erneux, C
    Onaya, T
    BIOCHEMICAL JOURNAL, 1997, 326 : 221 - 225
  • [23] PURIFICATION OF D-MYO-INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE FROM RAT-BRAIN
    JOHANSON, RA
    HANSEN, CA
    WILLIAMSON, JR
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1988, 263 (16) : 7465 - 7471
  • [24] Intrinsic inhibitor of inositol 1,4,5-trisphosphate binding
    Masato Hirata
    Masako Yoshida
    Takashida Kanematsu
    Hiroshi Takeuchi
    Molecular and Cellular Biochemistry, 1999, 190 : 179 - 184
  • [25] PARTIAL-PURIFICATION AND SOME PROPERTIES OF RAT-BRAIN INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE
    MORRIS, AJ
    MURRAY, KJ
    ENGLAND, PJ
    DOWNES, CP
    MICHELL, RH
    BIOCHEMICAL JOURNAL, 1988, 251 (01) : 157 - 163
  • [26] Elevated [3H]inositol 1,4,5-trisphosphate binding sites and expressed inositol 1,4,5-trisphosphate receptor protein level in platelets of depressed patients
    Yogesh Dwivedi
    Philip G. Janicak
    G. N. Pandey
    Psychopharmacology, 1998, 138 : 47 - 54
  • [27] INOSITOL 1,4,5-TRISPHOSPHATE INDUCED MOBILIZATION OF CA-2+ FROM RAT-BRAIN SYNAPTOSOMES
    GANDHI, CR
    ROSS, DH
    NEUROCHEMICAL RESEARCH, 1987, 12 (01) : 67 - 72
  • [28] EFFECT OF INOSITOL TETRAKISPHOSPHATES ON INOSITOL 1,4,5-TRISPHOSPHATE BINDING TO RAT-LIVER MICROSOMES
    TONES, MA
    BOOTMAN, MD
    PAY, GF
    BIOCHEMICAL SOCIETY TRANSACTIONS, 1988, 16 (04) : 593 - 593
  • [29] Autoradiographic characterization of [H-3]inositol(1,4,5)trisphosphate and [H-3]inositol(1,3,4,5)tetrakisphosphate binding sites in human brain
    Kurumatani, T
    Cowburn, RF
    Bogdanovic, N
    Winblad, B
    Fastbom, J
    JOURNAL OF NEURAL TRANSMISSION, 1997, 104 (2-3) : 175 - 189
  • [30] The inositol 1,4,5-trisphosphate receptors
    Bezprozvanny, I
    CELL CALCIUM, 2005, 38 (3-4) : 261 - 272