Shimizu Takahiro, Shimizu Shogo, Wada Naoki, Takai Shun, Shimizu Nobutaka, Higashi Youichirou, Kadekawa Katsumi, Majima Tsuyoshi, Saito Motoaki, Yoshimura Naoki
Department of Pharmacology, Kochi Medical School, Kochi University, Nankoku, Kochi, Japan.
Department of Urology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Br J Pharmacol. 2017 Sep;174(18):3072-3080. doi: 10.1111/bph.13941. Epub 2017 Aug 3.
Psychological stress exacerbates symptoms of urinary bladder dysfunction; however, the underlying brain mechanisms are unclear. We have demonstrated that centrally administered bombesin, a stress-related neuropeptide, facilitates the rat micturition reflex. Brain bombesin-like peptides modulate the serotoninergic nervous system activity under stress conditions; therefore, we examined whether brain 5-HT is involved in the bombesin-induced increased frequency of urination in urethane-anaesthetised male Sprague-Dawley rats.
Evaluation of intercontraction intervals (ICI) and maximal voiding pressure (MVP) during cystometrograms were started 1 h before i.c.v. administration of bombesin or i.c.v. pretreatment with the 5-HT receptor antagonists.
Bombesin (0.03 nmol per animal, i.c.v.) significantly reduced ICI without affecting MVP. The bombesin-induced response was significantly suppressed by acute depletion of brain 5-HT, which was induced by pretreatment with p-chlorophenylalanine, a 5-HT synthesis inhibitor. Bombesin at a lower dose (0.01 nmol per animal, i.c.v.) showed no significant effect on ICI, while it significantly reduced ICI in the presence of WAY-100635 (5-HT receptor antagonist, 0.1 or 0.3 μg per animal, i.c.v.), which can block the negative feedback control of 5-HT release. Bombesin (0.03 nmol per animal)-induced ICI reduction was significantly attenuated by SB269970 (5-HT receptor antagonist, 0.1 or 0.3 μg per animal, i.c.v.) but not by ritanserin (5-HT receptor antagonist, 0.3 or 1 μg per animal, i.c.v.).
The brain serotoninergic nervous system is involved in the facilitation of the rat micturition reflex induced by bombesin-like peptides at least in part through brain 5-HT receptors.
心理应激会加剧膀胱功能障碍的症状;然而,其潜在的脑机制尚不清楚。我们已经证明,中枢给予蛙皮素(一种与应激相关的神经肽)可促进大鼠排尿反射。脑内类似蛙皮素的肽在应激条件下调节血清素能神经系统的活性;因此,我们研究了脑内5-羟色胺(5-HT)是否参与了在乌拉坦麻醉的雄性斯普拉格-道利大鼠中蛙皮素诱导的排尿频率增加。
在脑室内注射蛙皮素或用5-HT受体拮抗剂进行脑室内预处理前1小时,开始评估膀胱内压描记图期间的收缩间隔(ICI)和最大排尿压力(MVP)。
蛙皮素(每只动物0.03 nmol,脑室内注射)显著缩短ICI,而不影响MVP。5-HT合成抑制剂对氯苯丙氨酸预处理诱导的脑内5-HT急性耗竭可显著抑制蛙皮素诱导的反应。较低剂量的蛙皮素(每只动物0.01 nmol,脑室内注射)对ICI无显著影响,而在存在WAY-100635(5-HT受体拮抗剂,每只动物0.1或0.3 μg,脑室内注射)时可显著缩短ICI,WAY-100635可阻断5-HT释放的负反馈控制。蛙皮素(每只动物0.03 nmol)诱导的ICI缩短被SB269970(5-HT受体拮抗剂,每只动物0.1或0.3 μg,脑室内注射)显著减弱,但未被利坦色林(5-HT受体拮抗剂,每只动物0.3或1 μg,脑室内注射)减弱。
脑内血清素能神经系统至少部分通过脑内5-HT受体参与了类似蛙皮素的肽诱导的大鼠排尿反射的促进作用。