Demonstration of 5-HT3 receptor function and expression in the mouse bladder

被引:17
作者
Chetty, N.
Coupar, I. M.
Chess-Williams, R.
Kerr, K. P. [1 ]
机构
[1] Monash Univ, Victorian Coll Pharm, Dept Pharmaceut Biol, Parkville, Vic 3052, Australia
[2] Bond Univ, Fac Hlth Sci & Med, Gold Coast, Qld 4229, Australia
[3] Monash Univ, Victorian Coll Pharm, Dept Pharmacol, Parkville, Vic 3052, Australia
关键词
mouse bladder center dot 5-HT3 receptor; field-stimulated contractions; ondansetron; meta-chloro-phenylbiguanide;
D O I
10.1007/s00210-007-0173-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to demonstrate the presence of 5-HT3 receptors in the mouse bladder and to determine their location. Bladder strips from female mice were set up in gassed Krebs-Henseleit solution at 37 degrees C and contractions recorded in response to electrical field stimulation (8 Hz, 60 V, 0.5-ms pulse duration) applied for 2 s every 50 s. The potentiating effects of 5-hydroxytryptamine (5-HT) were recorded (in the presence of 1-mu M methysergide and 1-mu M GR125487 to isolate the 5-HT3 receptor response), and contractions were expressed as a percentage of the response to 0.1-M KCl. Responses to (5-HT) were also obtained in the presence of the 5-HT3 receptor antagonist, ondansetron. RT-PCR was used to detect the expression of the 5-HT3A and 5-HT3B subunit transcripts of the mouse 5-HT3 receptor. 5-HT and 5-HT3 receptor agonists caused concentration-dependent increases in the force of neurogenic contractions without affecting the baseline tone. The rank order of potency was: meta-chloro-phenylbiguanide (m-CPB) = 5-HT > 2-methyl-5-HT (2m5-HT) = 1-phenylbiguanide (1-PBG). The respective pEC(50) values were: 6.42 +/- 0.2=5.95 +/- 0.19 > 5.35 +/- 0.12=5.14 +/- 0.13. m-CPB acted as a full agonist (E (max)=40.65 +/- 3.81% KCl), but both 2m5-HT and 1-PBG acted as lower potency partial agonists. Ondansetron (30, 100, 300 nM) caused concentration-related rightward displacements to the concentration-effect curve to 5-HT. Nonlinear regression analysis of the effect of the ondansetron concentrations on the pEC(50) values produced a pK(B) value of 8.29 +/- 0.22. Desensitization of sensory nerves to the contractile effect of capsaicin (10 mu M for 60 min) did not alter the ability of 5-HT to potentiate neurogenic contractions. 5-HT (3 mu M) inhibited contractions induced by direct muscle stimulation (lignocaine, 300 mu M and 10-ms pulse width). m-CPB also caused the same effect with a pIC(50) of 6.62 +/- 0.10 and an E (max) of 48.03 +/- 2.25%. The concentration-response curve to m-CPB was shifted rightwards by ondansetron (1 mu M) giving an apparent pK(B) value of 8.15 +/- 0.33. mRNA for both the 5-HT3A and 5-HT3B receptor subunits was detected in the detrusor as well as the mucosa with a greater relative expression of the 5-HT3A subunit in both layers. This study demonstrates that 5-HT mediates enhanced neurogenic contractions of the mouse bladder muscle by an action at 5-HT3 receptors located prejunctionally on nonsensory nerve elements. Additionally, an inhibitory postjunctional population of the 5-HT3 receptor was identified. The presence of the 5-HT3 receptor was confirmed by the expression of both 5-HT3A and 5-HT3B receptor subunits of the 5-HT3 receptor.
引用
收藏
页码:359 / 368
页数:10
相关论文
共 35 条
[1]   POSSIBLE INVOLVEMENT OF ADENINE-NUCLEOTIDES IN THE NEUROTRANSMISSION OF THE MOUSE URINARY-BLADDER [J].
ACEVEDO, CG ;
CONTRERAS, E .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 1985, 82 (02) :357-361
[2]  
Alexander SPH, 2004, BRIT J PHARMACOL, V141, pS1
[3]   SOME QUANTITATIVE USES OF DRUG ANTAGONISTS [J].
ARUNLAKSHANA, O ;
SCHILD, HO .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1959, 14 (01) :48-58
[4]   Characterisation of the 5-HT receptor potentiating neurotransmission in rabbit bladder [J].
Barras, M ;
VanderGraaf, PH ;
Angel, I .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 318 (2-3) :425-428
[5]   A quantitative study of atropine-resistant contractile responses in human detrusor smooth muscle, from stable, unstable and obstructed bladders [J].
Bayliss, M ;
Wu, C ;
Newgreen, D ;
Mundy, AR ;
Fry, CH .
JOURNAL OF UROLOGY, 1999, 162 (05) :1833-1839
[6]   EFFECTS OF CAPSAICIN DESENSITIZATION ON THE STIMULATORY EFFECT OF KININS, PROSTAGLANDINS, BIOGENIC-AMINES AND VARIOUS DRUGS IN GUINEA-PIG ISOLATED ATRIA [J].
BERNOUSSI, A ;
RIOUX, F .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 96 (03) :563-572
[7]   Uropathic observations in mice expressing a constitutively active point mutation in the 5-HT3A receptor subunit [J].
Bhattacharya, A ;
Dang, H ;
Zhu, QM ;
Schnegelsberg, B ;
Rozengurt, N ;
Cain, G ;
Prantil, R ;
Vorp, DA ;
Guy, N ;
Julius, D ;
Ford, APDW ;
Lester, HA ;
Cockayne, DA .
JOURNAL OF NEUROSCIENCE, 2004, 24 (24) :5537-5548
[8]   THE ENANTIOMERS OF ZACOPRIDE - AN INTRASPECIES COMPARISON OF THEIR POTENCIES IN FUNCTIONAL AND ANXIOLYTIC MODELS [J].
BILL, DJ ;
COLEMAN, J ;
HALLETT, I ;
MIDDLEFELL, V ;
RHODES, KF ;
FLETCHER, A .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 115 (05) :775-780
[9]   Serotonin-induced potentiation of cholinergic responses to electrical field stimulation in normal and neurogenic overactive human detrusor muscle [J].
Chapple, CR ;
Radley, SC ;
Martin, SW ;
Sellers, DJ ;
Chess-Williams, R .
BJU INTERNATIONAL, 2004, 93 (04) :599-604
[10]   Activation of 5-HT3 receptors in the rat and mouse intestinal tract:: a comparative study [J].
Chetty, Navinisha ;
Irving, Helen R. ;
Coupar, Ian M. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 148 (07) :1012-1021