Ferulic acid suppresses guinea pig ileal longitudinal smooth muscle contractions by inhibiting voltage-dependent Ca2+ channels

We investigated the effects of ferulic acid (FA) on contractions in guinea pig ileal longitudinal smooth muscle (ILSM). FA (3 × 10<sup>-4</sup>-3 × 10<sup>-3</sup> M) inhibited ILSM contractions induced by acetylcholine, histamine, prostaglandin F<sub>2α</sub>, and serotonin concentration-dependently, reversibly, and noncompetitively with pD'<sub>2</sub> values of ∼3. FA also concentration-dependently and reversibly inhibited KCl-induced ILSM contractions. FA (10<sup>-3</sup> M), which inhibited ILSM contractions by ∼50 %, also reduced verapamil-sensitive, KCl-induced intracellular Ca<sup>2+</sup> increases in A7r5 cells by ∼35 %. These results suggest that FA inhibits ILSM contraction, primarily through the reversible inhibition of Ca<sup>2+</sup> influx via voltage-dependent Ca<sup>2+</sup> channels.

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Publication Details

Journal
Journal of Pharmacological Sciences
Published
2025-05-14
DOI
https://doi.org/10.1016/j.jphs.2025.05.012
Citations
2
Primary Topic
Pharmacological Effects of Natural Compounds
Type
article
Field-Weighted Citation Impact
3.11

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article

Ferulic acid suppresses guinea pig ileal longitudinal smooth muscle contractions by inhibiting voltage-dependent Ca2+ channels

Masakazu Enomoto, Yoshio Tanaka, Kento Yoshioka, Keisuke Obara et al.
2 citations
Journal of Pharmacological Sciences
Pharmacological Effects of Natural Compounds
3.11
article

Ferulic acid suppresses guinea pig ileal longitudinal smooth muscle contractions by inhibiting voltage-dependent Ca2+ channels

Masakazu Enomoto, Yoshio Tanaka, Kento Yoshioka, Keisuke Obara, Fumiaki Makino, Shin-Ichiro Ichihara, Naho Takazakura, Aya Shimada, Wakaba Kinami
article en
2 citations

Abstract

We investigated the effects of ferulic acid (FA) on contractions in guinea pig ileal longitudinal smooth muscle (ILSM). FA (3 × 10<sup>-4</sup>-3 × 10<sup>-3</sup> M) inhibited ILSM contractions induced by acetylcholine, histamine, prostaglandin F<sub>2α</sub>, and serotonin concentration-dependently, reversibly, and noncompetitively with pD'<sub>2</sub> values of ∼3. FA also concentration-dependently and reversibly inhibited KCl-induced ILSM contractions. FA (10<sup>-3</sup> M), which inhibited ILSM contractions by ∼50 %, also reduced verapamil-sensitive, KCl-induced intracellular Ca<sup>2+</sup> increases in A7r5 cells by ∼35 %. These results suggest that FA inhibits ILSM contraction, primarily through the reversible inhibition of Ca<sup>2+</sup> influx via voltage-dependent Ca<sup>2+</sup> channels.

Journal of Pharmacological SciencesVol. 158(4)
Toho University (JP)
Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 10%
Pharmacological Effects of Natural Compounds
3.11
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