Further investigation of the effects of 5-hydroxytryptamine, 8-OH-DPAT and DOI to mediate contraction and relaxation responses in the intestine and emesis in Suncus murinus

Eur J Pharmacol. 2018 Feb 15:821:79-87. doi: 10.1016/j.ejphar.2017.12.051. Epub 2017 Dec 23.

Abstract

5-HT receptors are implicated in many gastrointestinal disorders. However, the precise role of 5-HT in mediating GI responses in Suncus murnius is still unclear. Therefore in this study, the effects of 5-HT and its agonists were investigated in Suncus. The involvement of 5-HT2C receptors in mediating emesis was also investigated. The ability of 5-HT and its agonists/antagonists at 5-HT1A and 5-HT2 to modify GI motility was investigated in vitro and in vivo. WAY100635 (a 5-HT1A antagonist) inhibited the contraction response to 5-HT in the proximal segments without affecting the maximum response; whilst enhancing the contraction to 5-HT (>30.0nM) in the distal intestine. The selective 5-HT2A and 5-HT2B receptor antagonists MDL-100907 and RS-127445 attenuated 5-HT-induced contractions (<10.0µM) in the distal segments. RS-127445 also attenuated 5-HT-induced contractions in the central segments. The selective 5-HT2C receptor antagonist SB-242084, attenuated the responses to 5-HT (> 3.0nM) in the proximal and central but not the distal regions. 8-OH-DPAT-induced relaxation was resistant to the antagonism by 5-HT1A/7 antagonists. DOI in the presence of 5-HT1A/2A/2B/2C antagonists induced greater contraction responses (>1.0µM) in most tissues, whilst RS-127445, or SB-242084, reduced the responses to DOI (< 1.0µM) in some tissues. SB-242084 also suppressed emesis-induced by motion and intragastric CuSO4. In conclusion, within different regions of intestine, 5-HT2 receptors are differently involved in contraction and emetic responses and that 8-OH-DPAT induces relaxation via non-5-HT1A/7 receptors. Suncus could provide a model to investigate these diverse actions of 5-HT.

Keywords: 5-HT(1A) and 5-HT(2) receptor subtypes; 5-Hydroxytryptamine; 8-OH-DPAT; DOI; Suncus murinus intestine.

MeSH terms

  • 8-Hydroxy-2-(di-n-propylamino)tetralin / pharmacology*
  • Aminopyridines / pharmacology
  • Amphetamines / pharmacology*
  • Animals
  • Female
  • Fluorobenzenes / pharmacology
  • In Vitro Techniques
  • Indoles / pharmacology
  • Intestine, Small / drug effects
  • Male
  • Muscle Contraction / drug effects*
  • Muscle Contraction / physiology
  • Muscle Relaxation / drug effects*
  • Muscle Relaxation / physiology
  • Piperazines / pharmacology
  • Piperidines / pharmacology
  • Pyridines / pharmacology
  • Pyrimidines / pharmacology
  • Receptor, Serotonin, 5-HT2C / physiology
  • Serotonin / pharmacology*
  • Serotonin / physiology*
  • Serotonin 5-HT1 Receptor Antagonists / pharmacology
  • Serotonin 5-HT2 Receptor Antagonists / pharmacology
  • Serotonin Receptor Agonists / pharmacology
  • Shrews
  • Vomiting / chemically induced
  • Vomiting / physiopathology*

Substances

  • 6-chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline
  • Aminopyridines
  • Amphetamines
  • Fluorobenzenes
  • Indoles
  • Piperazines
  • Piperidines
  • Pyridines
  • Pyrimidines
  • Receptor, Serotonin, 5-HT2C
  • Serotonin 5-HT1 Receptor Antagonists
  • Serotonin 5-HT2 Receptor Antagonists
  • Serotonin Receptor Agonists
  • 2-amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyrimidine
  • Serotonin
  • N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide
  • 8-Hydroxy-2-(di-n-propylamino)tetralin
  • volinanserin
  • 4-iodo-2,5-dimethoxyphenylisopropylamine