Roles of Na+/Ca2+ exchanger isoforms NCX1 and NCX2 in motility in mouse ileum

Kazuhiro Nishiyama, Yasu Taka Azuma, Ai Morioka, Natsuho Yoshida, Midori Teramoto, Kohta Tanioka, Satomi Kita, Satomi Hayashi, Hidemitsu Nakajima, Takahiro Iwamoto, Tadayoshi Takeuchi

Research output: Contribution to journalArticlepeer-review

Abstract

The Na+/Ca2+ exchanger (NCX) is a plasma membrane transporter that is involved in regulating intracellular Ca2+ concentrations in various tissues. The physiological roles by which NCX influences gastrointestinal motility are incompletely understood, although its role in the heart, brain, and kidney has been widely investigated. In this study, we focused on the functions of the NCX isoforms, NCX1 and NCX2, in the motility of the ileum in the gastrointestinal tract. We investigated the response to electric field stimulation (EFS) in the longitudinal smooth muscle of the ileum obtained from wild-type mice (WT), NCX1-heterozygote knockout mice (NCX1 HET), NCX2 HET and smooth muscle-specific NCX1.3 transgenic mice (NCX1.3 Tg). EFS induced a phasic contraction that persisted during EFS and a tonic contraction that occurred after the end of EFS. We found that the amplitudes of the phasic and tonic contractions were significantly smaller in NCX2 HET, but not in NCX1 HET, compared to WT. Moreover, the magnitudes of acetylcholine (ACh)- and substance P (SP)-induced contractions of NCX2 HET, but not of NCX1 HET, were smaller compared to WT. In contrast, the amplitudes of the phasic and tonic contractions were greater in NCX1.3 Tg compared to WT. Similar to EFS, the magnitude of ACh-induced contraction was greater in NCX1.3 Tg than in WT. Taken together, our findings indicated that NCX1 and NCX2 play important roles in ileal motility and suggest that NCX1 and NCX2 regulate the motility in the ileum by controlling the sensitivity of smooth muscles to ACh and SP.

Original languageEnglish
Pages (from-to)1081-1090
Number of pages10
JournalNaunyn-Schmiedeberg's Archives of Pharmacology
Volume389
Issue number10
DOIs
Publication statusPublished - Oct 1 2016
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Pharmacology

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