The adenosine A1 receptor agonist N6-cyclopentyladenosine blocks the disruptive effect of phencyclidine on prepulse inhibition of the acoustic startle response in the rat

被引:28
|
作者
Sills, TL [1 ]
Azampanah, A [1 ]
Fletcher, PJ [1 ]
机构
[1] Clarke Inst Psychiat, Clarke Div, Ctr Addict & Ment Hlth, Biopsychol Sect, Toronto, ON M5T 1R8, Canada
关键词
acoustic startle response; NMDA receptor antagonist; phencyclidine; prepulse inhibition;
D O I
10.1016/S0014-2999(99)00088-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Systemic administration of the NMDA receptor antagonist phencyclidine (PCP; 4 mg/kg) produced a profound reduction in prepulse inhibition of the acoustic startle response in rats. Pre-treatment with the selective adenosine A(1) receptor agonist N-6-cyclopentyladenosine (CPA) blocked (0.5 mg/kg) or attenuated (0.1 and 0.2 mg/kg) the disruptive effect of PCP an prepulse inhibition. These findings suggest that adenosine may regulate the inhibitory effect of NMDA receptor blockade on prepulse inhibition, and raise the possibility that adenosine may be a potentially useful target for anti-psychotic medication. Further, 0.5 mg/kg CPA by itself was without effect on prepulse inhibition but did decrease startle amplitude, raising the possibility that adenosine, acting via A(1) receptors, may be a component of the neurochemical substrate that modulates the acoustic startle response. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:325 / 329
页数:5
相关论文
共 50 条
  • [1] Mechanisms of acetylcholinesterase protection against sarin and soman by adenosine A1 receptor agonist N6-cyclopentyladenosine
    Beste, Ariana
    Taylor, DeCarlos E.
    Shih, Tsung-Ming
    Thomas, Thaddeus P.
    COMPUTATIONAL BIOLOGY AND CHEMISTRY, 2018, 75 : 74 - 81
  • [2] Therapeutic efficacy of the adenosine A1 receptor agonist N6-cyclopentyladenosine (CPA) against organophosphate intoxication
    Bueters, TJH
    Groen, B
    Danhof, M
    IJzerman, AP
    van Helden, HPM
    ARCHIVES OF TOXICOLOGY, 2002, 76 (11) : 650 - 656
  • [3] Interaction of the adenosine A1 receptor agonist N6-cyclopentyladenosine and κ-opioid receptors in rat spinal cord nociceptive reflexes
    Ramos-Zepeda, Guillermo A.
    Herrero-Zorita, Carlos
    Herrero, Juan F.
    BEHAVIOURAL PHARMACOLOGY, 2014, 25 (08): : 741 - 749
  • [4] Therapeutic efficacy of the adenosine A1 receptor agonist N6-cyclopentyladenosine (CPA) against organophosphate intoxication
    Tjerk J. Bueters
    Bas Groen
    Meindert Danhof
    Ad P. IJzerman
    Herman P. van Helden
    Archives of Toxicology, 2002, 76 : 650 - 656
  • [5] Adenosine A1 receptor agonist N6-cyclopentyladenosine affects the inactivation of acetylcholinesterase in blood and brain by sarin
    Bueters, TJH
    Joosen, MJA
    van Helden, HPM
    IJzerman, P
    Danhof, M
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (03): : 1307 - 1313
  • [6] Determination of the adenosine A1 agonist N6-cyclopentyladenosine in rat blood by solid-phase extraction and HPLC
    Scalia, S
    Simeoni, S
    Dalpiaz, A
    Villani, S
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2001, 24 (5-6) : 1131 - 1136
  • [7] Interaction of the adenosine A1 receptor agonist N6-cyclopentyladenosine (CPA) and opioid receptors in spinal cord nociceptive reflexes
    Ramos-Zepeda, Guillermo
    Herrero, Juan F.
    LIFE SCIENCES, 2013, 93 (5-6) : 233 - 239
  • [8] Synthesis and Study of 5′-Ester Prodrugs of N6-Cyclopentyladenosine, a Selective A1 Receptor Agonist
    Alessandro Dalpiaz
    Angelo Scatturin
    Enea Menegatti
    Fabrizio Bortolotti
    Barbara Pavan
    Carla Biondi
    Elisa Durini
    Stefano Manfredini
    Pharmaceutical Research, 2001, 18 : 531 - 536
  • [9] Cardiovascular effects of the adenosine A1 receptor agonist N6-cyclopentyladenosine (CPA) decisive for its therapeutic efficacy in sarin poisoning
    Joosen, MJA
    Bueters, TJH
    van Helden, HPM
    ARCHIVES OF TOXICOLOGY, 2004, 78 (01) : 34 - 39
  • [10] Cardiovascular effects of the adenosine A1 receptor agonist N6-cyclopentyladenosine (CPA) decisive for its therapeutic efficacy in sarin poisoning
    Marloes J. A. Joosen
    Tjerk J. H. Bueters
    Herman P. M. van Helden
    Archives of Toxicology, 2004, 78 : 34 - 39