首页> 美国卫生研究院文献>World Journal of Gastroenterology >Tegaserod inhibits noxious rectal distention induced responses and limbic system c-Fos expression in rats with visceral hypersensitivity
【2h】

Tegaserod inhibits noxious rectal distention induced responses and limbic system c-Fos expression in rats with visceral hypersensitivity

机译:Tegaserod抑制内脏超敏性大鼠中有害的直肠扩张诱发的反应和边缘系统c-Fos表达

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

AIM: To examine the effects of tegaserod, a serotonin (5-HT) 4 receptor partial agonist, on abdominal withdrawal reflex (AWR) to rectal distention (RD) and c-Fos expression in limbic system.METHODS: Neonatal Sprague-Dawley rats randomly received colonic irritation by acetic acid from postnatal day 8 to day 21 as a visceral hypersensitive model (group H) or by intrarectal saline as a control group (group C). When they became adults, rectal distention (RD) was performed by a balloon (6F; Fogarty arterial embolectomy catheter; length, 20 mm; diameter, 2 mm) which was rapidly inflated with increasing volumes of saline (0.4, 0.8 and 1.2 mL) for 20 s at five-minute intervals. Five subgroups of group H (H-saline, H-vehicle, H-Teg0.1, H-Teg0.3 and H-Teg1.0) were injected randomly with saline, vehicle (1-methyl-2-thpyrrolidone) or tegaserod at doses of 0.1, 0.3 and 1.0 mg/kg ip, respectively. Two subgroups of group C (C-Saline and C-Teg1.0) were injected with saline or tegaserod (1.0 mg/kg) ip. RD was performed 10 min after injection, AWR was recorded and c-Fos expression in limbic system was analyzed quantitatively by immunohistochemistry.RESULTS: Compared to saline, tegaserod significantly inhibited AWR in group H (0.4 mL: from 2.0 to 0.5; 0.8 mL: from 3.5 to 1.5; 1.2 mL: from 4.0 to 3.0, P < 0.01), but had no significant effect on group C. Tegaserod dose-dependently attenuated the number of c-Fos positive neurons in limbic structures, anterior cingulate cortex (ACC) showed the greatest attenuation. In group H, tegaserod (1.0 mg/kg) resulted in a significant overall decrease to 57% of H-saline (283 ± 41 vs 162 ± 16, P < 0.01), in ACC to 42% of H-saline (72 ± 10 vs 31 ± 8, P < 0.01). In group C, tegaserod (1.0 mg/kg) resulted in an overall decrease to 77% of C-saline (214 ± 13 vs 164 ± 22, P < 0.01), in ACC to 65% of C-saline (48 ± 8 vs 31 ± 7, P < 0.01).CONCLUSION: Tegaserod inhibits the response to rectal distention in rats with visceral hypersensitivity and dose-dependently attenuates c-Fos expression in limbic system, especially in anterior cingulate cortex.
机译:目的:研究5-羟色胺(5-HT)4受体部分激动剂替加色罗对腹侧反射(AWR)至直肠扩张(RD)和角膜缘系统中c-Fos表达的影响。方法:新生Sprague-Dawley大鼠从出生后第8天到第21天,随机接受乙酸作为内脏超敏模型的结肠刺激(H组)或直肠内生理盐水作为对照组(C组)。成年后,用气球(6F; Fogarty动脉栓塞切除术导管;长度20 mm;直径2 mm)进行直肠扩张(RD),并随着生理盐水(0.4、0.8和1.2 mL)的增加而迅速膨胀每五分钟间隔20 s。 H组的五个亚组(H-盐水,H-车辆,H-Teg0.1,H-Teg0.3和H-Teg1.0)随机注射生理盐水,媒介物(1-甲基-2-噻咯烷酮)或替加色罗剂量分别为0.1、0.3和1.0 mg / kg ip。 C组的两个亚组(C-盐水和C-Teg1.0)腹腔注射盐水或替加色罗(1.0 mg / kg)。注射后10分钟进行RD,记录AWR并通过免疫组织化学定量分析边缘系统中的c-Fos表达。结果:与生理盐水相比,替加色罗显着抑制H组的AWR(0.4 mL:从2.0至0.5; 0.8 mL:从3.5到1.5;从1.2毫升:从4.0到3.0,P <0.01),但对C组无显着影响。替加色罗剂量依赖性地减弱边缘结构,前扣带回皮质(ACC)中c-Fos阳性神经元的数量表现出最大的衰减。在H组中,替加色罗(1.0 mg / kg)导致总体总体显着降低至H-盐水的57%(283±41 vs 162±16,P <0.01),在ACC中降至42%的H-盐水(72± 10 vs 31±8,P <0.01)。 C组中,替加色罗(1.0 mg / kg)导致ACC总体下降至77%的C-盐水(214±13 vs 164±22,P <0.01),C-盐水的65%(48±8) vs 31±7,P <0.01)。结论:替加色罗抑制内脏超敏性大鼠对直肠扩张的反应,并剂量依赖性地减弱边缘系统(尤其是前扣带回皮质)中的c-Fos表达。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号