The effects of cyclophosphamide on neurotransmission in the urinary bladder of Suncus murinus, the house musk shrew

被引:21
作者
Mok, MHS
Knight, GE
Andrews, PLR
Hoyle, CHV
Burnstock, G
机构
[1] Royal Free & Univ Coll Med Sch, Auton Neurosci Inst, London NW3 2PF, England
[2] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
[3] Univ London St Georges Hosp, Sch Med, Dept Physiol, London SW17 0RE, England
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 2000年 / 80卷 / 03期
关键词
ATP; carbachol; cotransmission; cyclophosphamide; purinoceptor; Suncus; urinary bladder;
D O I
10.1016/S0165-1838(00)00085-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study has shown that cyclaphosphamide treatment of the insectivore Suncus murinus, causes a down regulation in both muscarinic and P2X receptors, together with a reduced responsiveness to exogenous histamine (0.3 mM) in the urinary bladder. Electrical field stimulation (70 V, 0.3 ms, 0.5-16 Hz, 10 s every 5 min) of bladders from both control and cyclophosphamide-treated animals showed identical responses. Since post-junctional alterations have been revealed by the reduced responsiveness to exogenous carbachol (0.1 mu M-3 mM) and beta,gamma-methylene ATP (0.3-300 mu M), it would appear that in the bladders of cyclophosphamide-treated animals there is also a pre-junctional effect, increased transmitter release compensating for the down regulation of the receptors. As the pattern of neurotransmission of the bladder of suncus more closely resembles that of human detrusor than other commonly studied laboratory animals, this insectivore appears to be a useful animal model for the study of bladder neurotransmission in pathophysiological conditions. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:130 / 136
页数:7
相关论文
共 34 条
[1]   CHARACTERIZATION OF THE CAPSAICIN-SENSITIVE COMPONENT OF CYCLOPHOSPHAMIDE-INDUCED INFLAMMATION IN THE RAT URINARY-BLADDER [J].
AHLUWALIA, A ;
MAGGI, CA ;
SANTICIOLI, P ;
LECCI, A ;
GIULIANI, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1994, 111 (04) :1017-1022
[2]   The NK1 antagonist GR203040 inhibits cyclophosphamide-induced damage in the rat and ferret bladder [J].
Alfieri, A ;
Gardner, C .
GENERAL PHARMACOLOGY, 1997, 29 (02) :245-250
[3]   The pharmacology of the emetic response to upper gastrointestinal tract stimulation in Suncus murinus [J].
Andrews, P ;
Torii, Y ;
Saito, H ;
Matsuki, N .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 307 (03) :305-313
[4]   Cyclophosphamide cystitis as a model of visceral pain in rats. A survey of hindbrain structures involved in visceroception and nociception using the expression of c-Fos and Krox-24 proteins [J].
Bon, K ;
LanteriMinet, M ;
dePommery, J ;
Michiels, JF ;
Menetrey, D .
EXPERIMENTAL BRAIN RESEARCH, 1996, 108 (03) :404-416
[5]   STUDIES ON THE UROTOXICITY OF OXAZAPHOSPHORINE CYTOSTATICS AND ITS PREVENTION .1. EXPERIMENTAL STUDIES ON THE UROTOXICITY OF ALKYLATING COMPOUNDS [J].
BROCK, N ;
POHL, J ;
STEKAR, J .
EUROPEAN JOURNAL OF CANCER, 1981, 17 (06) :595-607
[6]   ATROPINE RESISTANT EXCITATION OF URINARY-BLADDER - POSSIBILITY OF TRANSMISSION VIA NERVES RELEASING A PURINE NUCLEOTIDE [J].
BURNSTOCK, G ;
SMYTHE, A ;
DUMSDAY, B .
BRITISH JOURNAL OF PHARMACOLOGY, 1972, 44 (03) :451-+
[7]  
COLBERT EH, 1958, EVOLUTION VERTEBRATE
[8]   CYCLOPHOSPHAMIDE CYSTITIS - IDENTIFICATION OF ACROLEIN AS THE CAUSATIVE AGENT [J].
COX, PJ .
BIOCHEMICAL PHARMACOLOGY, 1979, 28 (13) :2045-2049
[9]  
DEVRIES CR, 1990, J UROLOGY, V143, P1
[10]   INCREASED URINE HISTAMINE AND METHYLHISTAMINE IN INTERSTITIAL CYSTITIS [J].
ELMANSOURY, M ;
BOUCHER, W ;
SANT, GR ;
THEOHARIDES, TC .
JOURNAL OF UROLOGY, 1994, 152 (02) :350-353