Taniguchi Hiroshi, Ariga Hajime, Zheng Jun, Ludwig Kirk, Mantyh Christopher, Pappas Theodore N, Takahashi Toku
Department of Surgery, Duke University Medical Center, Durham, North Carolina, USA.
Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G403-11. doi: 10.1152/ajpgi.90260.2008. Epub 2008 Jun 19.
Endogenous ghrelin causes interdigestive contractions of the stomach in rats. In contrast, previous studies showed that 5-HT(3) and 5-HT(4) receptors were involved in regulating intestinal interdigestive contractions. We studied the possible role of endogenous ghrelin and 5-HT regulating interdigestive gastrointestinal (GI) contractions in rats. Four strain gauge transducers were implanted on the antrum, duodenum, and proximal and distal jejunum. After an overnight fast, GI contractions were recorded in freely moving conscious rats and ghrelin receptor antagonists [(d-lys3)GHRP6; 1 micromol/kg], 5-HT(3) antagonists (Ondansetron; 0.5 mg/kg) and 5-HT(4) antagonists (GR 125,487; 1 mg/kg) were administered (bolus iv). To evaluate the relationship between the luminal concentrations of 5-HT and phase III-like contractions of the duodenum, duodenal juice was collected via the intraduodenal catheter. 5-HT content of the duodenal juice was measured by HPLC. (d-lys3)GHRP6 significantly attenuated the occurrence and amplitude of phase III-like contractions of the antrum, but not the duodenum and jejunum. 5-HT(4) antagonists significantly reduced spontaneous phase III-like contractions of the jejunum, without affecting those of the antrum and duodenum. In contrast, 5-HT(3) antagonists did not affect phase III-like contractions in GI tract. Luminal concentration of 5-HT at the phase III-like contraction (36.0 +/- 13.3 ng/ml, n = 9) was significantly higher than that at the phase I-like contractions of the duodenum (4.9 +/- 1.6 ng/ml, n = 9, P < 0.05). It is suggested that released ghrelin from the gastric mucosa mediates gastric phase III-like contractions, whereas 5-HT released from enterochromaffin cells of the duodenal mucosa mediates intestinal phase III-like contractions via 5-HT(4) receptors.
内源性胃饥饿素可引起大鼠胃的消化间期收缩。相比之下,先前的研究表明,5-羟色胺(5-HT)3和5-HT4受体参与调节肠道消化间期收缩。我们研究了内源性胃饥饿素和5-HT在调节大鼠消化间期胃肠(GI)收缩中的可能作用。在胃窦、十二指肠以及空肠近端和远端植入四个应变片传感器。禁食过夜后,在自由活动的清醒大鼠中记录胃肠收缩,并静脉推注给予胃饥饿素受体拮抗剂[(d-lys3)GHRP6;1微摩尔/千克]、5-HT3拮抗剂(昂丹司琼;0.5毫克/千克)和5-HT4拮抗剂(GR 125,487;1毫克/千克)。为了评估十二指肠腔中5-HT浓度与十二指肠III期样收缩之间的关系,通过十二指肠内导管收集十二指肠液。采用高效液相色谱法测定十二指肠液中的5-HT含量。(d-lys3)GHRP6显著减弱了胃窦III期样收缩的发生频率和幅度,但对十二指肠和空肠的III期样收缩无影响。5-HT4拮抗剂显著减少了空肠的自发性III期样收缩,而不影响胃窦和十二指肠的III期样收缩。相比之下,5-HT3拮抗剂对胃肠道的III期样收缩无影响。III期样收缩时十二指肠腔中5-HT的浓度(36.0±13.3纳克/毫升,n = 9)显著高于十二指肠I期样收缩时的浓度(4.9±1.6纳克/毫升,n = 9,P < 0.05)。提示胃黏膜释放的胃饥饿素介导胃的III期样收缩,而十二指肠黏膜肠嗜铬细胞释放的5-HT通过5-HT4受体介导肠道的III期样收缩。