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替加色罗抑制内脏高敏感性大鼠有害直肠扩张诱导的反应及脊髓神经元型一氧化氮合酶表达

[Tegaserod inhibits noxious rectal distention induced response and spinal nNOS expression in rats with visceral hypersensitivity].

作者信息

Jiao Hong-mei, Xie Peng-yan

机构信息

Department of Gastroenterology, Peking University First Hospital, Beijing 100034, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2004 Aug 18;36(4):394-8.

Abstract

OBJECTIVE

To examine the effects of 5-HT4 receptor partial agonist tegaserod on response to rectal distention (RD) and on nNOS expression in spinal cord, and to investigate the mechanism of tegaserod influencing visceral sensation.

METHODS

Neonatal SD rats randomLy received colonic irritation by acetic acid from postnatal day 8 to day 21 as visceral hypersensitive model (Group H); or by saline intrarectally as control group (Group C). Five subgroups of Group H were i.p. injected randomLy with saline, vehicle (1-methyl-2-thpyrrolidone) or tegaserod at doses of 0.1, 0.3 and 1.0 mg/kg, respectively. Two subgroups of Group C were i.p. injected with saline or tegaserod at dose of 1.0 mg/kg. Ten minutes after injection rectal distention was performed, AWR was recorded and nNOS expression in spinal cord (L6-S1) was analyzed quantitatively by NADPH-diaphorase histochemistry.

RESULTS

Tegaserod significantly inhibited AWR in Group H, but had no effect in Group C. Tegaserod (1.0 mg/kg) inhibited AWR more significantly in Group H than in Group C at the largest volume of distention (1.2 mL). In Group H, tegaserod (1.0 mg/kg) significantly decreased overall nNOS positive cells in spinal cord to 40% of saline. The greatest attenuation was in dorsal horn (31% of H-saline). Tegaserod (0.1 mg/kg) did not affect the overall nNOS(P>0.20), but decreased the number of nNOS positive cells in central canal (79% of H-saline P<0.01).

CONCLUSION

Tegaserod inhibits response to rectal distention in rats with visceral hypersensitivity and dose dependently attenuates spinal nNOS expression, especially in dorsal horn and central canal. nNOS may be involved in the modulation of visceral sensitivity by tegaserod.

摘要

目的

研究5-羟色胺4(5-HT4)受体部分激动剂替加色罗对直肠扩张(RD)反应及脊髓中神经元型一氧化氮合酶(nNOS)表达的影响,探讨替加色罗影响内脏感觉的机制。

方法

新生SD大鼠从出生后第8天至第21天随机分为两组,一组用乙酸进行结肠刺激作为内脏高敏模型组(H组);另一组经直肠注入生理盐水作为对照组(C组)。H组再随机分为5个亚组,分别腹腔注射生理盐水、溶媒(1-甲基-2-吡咯烷酮)或剂量为0.1、0.3和1.0mg/kg的替加色罗。C组随机分为2个亚组,分别腹腔注射生理盐水或剂量为1.0mg/kg的替加色罗。注射10分钟后进行直肠扩张,记录腹壁回撤反射(AWR),并通过还原型辅酶Ⅱ黄递酶组织化学法定量分析脊髓(L6-S1)中nNOS的表达。

结果

替加色罗可显著抑制H组的AWR,但对C组无影响。在最大扩张容积(1.2mL)时,替加色罗(1.0mg/kg)对H组AWR的抑制作用比对C组更显著。在H组中,替加色罗(1.0mg/kg)可使脊髓中nNOS阳性细胞总数显著减少至生理盐水组的40%。最大降幅出现在背角(为H组生理盐水组的31%)。替加色罗(0.1mg/kg)对nNOS总数无影响(P>0.20),但可使中央管中nNOS阳性细胞数量减少(为H组生理盐水组的79%,P<0.01)。

结论

替加色罗可抑制内脏高敏大鼠对直肠扩张的反应,并剂量依赖性地减弱脊髓nNOS表达,尤其是在背角和中央管。nNOS可能参与替加色罗对内脏敏感性的调节。

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