Effects of tegaserod on Fos, substance P and calcitonin gene-related peptide expression induced by colon inflammation in lumbarsacral spinal cord

被引:26
作者
Sun, Yi-Ning [1 ]
Luo, Jin-Yan [1 ]
机构
[1] Xi An Jiao Tong Univ, Hosp 2, Dept Gastroenterol, Xian 710004, Shaanxi Provinc, Peoples R China
关键词
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the mechanisms of tegaserod, a partial 5-HT4 agonist, in reducing visceral sensitivity by observing Fos, substance P (SP) and calcitonin gene-related peptide (CGRP) expression in the lumbarsacral spinal cord induced by colonic inflammation in rats. METHODS: Twenty-four male rats with colonic inflammation induced by intraluminal instillation of trinitrobenzenesulfonic acid (TNBS) were divided into 3 groups. Treatment group 1: intra-gastric administration of tegaserod, 2 mg/kg . d; Treatment group 2: intra-gastric administration of tegaserod, 1 mg/kg . d; Control group: intra-gastric administration of saline, 2.0 mL/d. After 7 d of intra-gastric administration, lumbarsacral spinal cord was removed and processed for Fos, SP and CGRP immunohistochemistry. RESULTS: In rats of the control group, the majority of Fos labeled neurons was localized in deeper laminae of the lumbarsacral spinal cord (L5-S1). SP and CGRP were primarily expressed in the superficial laminae of the spinal cord after TNBS injection. Intra-gastric administration of tegaserod (2 mg/kg . d) resulted in a significant decrease of Fos labeled neurons (22.0+/-7.7) and SP density (12.5+/-1.4) in the dorsal horn in the lumbarsacral spinal cord compared to those of the control group (62.2+/-18.9, 35.9+/-8.9, P<0.05). However, CGRP content in dorsal horn did not significantly reduce in rats of treatment group 1 (1.2+/-1.1) compared to that of the control group (2.8+/-2.4, P>0.05). Neither Fos expression nor SP or CGRP density in the dorsal horn significantly declined in rats of treatment group 2 compared to those of the control group (P>0.05). CONCLUSION: Tegaserod can significantly reduce Fos labeled neurons in the lumbarsacral spinal cord induced by colonic inflammation. Tegaserod may reduce visceral sensitivity by inhibiting SP expression in the dorsal horn of spinal cord.
引用
收藏
页码:1830 / 1833
页数:4
相关论文
共 19 条
[1]
Bueno L, 1999, Can J Gastroenterol, V13 Suppl A, p42A
[2]
Mediators and pharmacology of visceral sensitivity: From basic to clinical investigations [J].
Bueno, L ;
Fioramonti, J ;
Delvaux, M ;
Frexinos, J .
GASTROENTEROLOGY, 1997, 112 (05) :1714-1743
[3]
CONTRIBUTION OF CENTRAL NEUROPLASTICITY TO PATHOLOGICAL PAIN - REVIEW OF CLINICAL AND EXPERIMENTAL-EVIDENCE [J].
CODERRE, TJ ;
KATZ, J ;
VACCARINO, AL ;
MELZACK, R .
PAIN, 1993, 52 (03) :259-285
[4]
Tegaserod, a 5-HT4 receptor partial agonist, decreases sensitivity to rectal distension in healthy subjects [J].
Coffin, B ;
Farmachidi, JP ;
Rueegg, P ;
Bastie, A ;
Bouhassira, D .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (04) :577-585
[5]
Involvement of prostaglandins and CGRP-dependent sensory afferents in peritoneal irritation-induced visceral pain [J].
Friese, N ;
Diop, L ;
Chevalier, E ;
Angel, F ;
Riviere, PJM ;
Dahl, SG .
REGULATORY PEPTIDES, 1997, 70 (01) :1-7
[6]
Central cholinergic antinociception induced by 5HT(4) agonists: BIMU 1 and BIMU 8 [J].
Ghelardini, C ;
Galeotti, N ;
Casamenti, F ;
MalmbergAiello, P ;
Pepeu, G ;
Gualtieri, F ;
Bartolini, A .
LIFE SCIENCES, 1996, 58 (25) :2297-2309
[7]
Pharmacology of serotonin as related to anesthesia [J].
Gyermek, L .
JOURNAL OF CLINICAL ANESTHESIA, 1996, 8 (05) :402-425
[8]
Orofacial deep and cutaneous tissue inflammation and trigeminal neuronal activation - Implications for persistent temporomandibular pain [J].
Imbe, H ;
Iwata, K ;
Zhou, QQ ;
Zou, SP ;
Dubner, R ;
Ren, K .
CELLS TISSUES ORGANS, 2001, 169 (03) :238-247
[9]
KISHIMOTO S, 1994, BIOMED RES-TOKYO, V15, P133
[10]
Tegaserod - A new 5-HT4 agonist [J].
Lacy, BE ;
Yu, SY .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2002, 34 (01) :27-33