Enhancement of receptor‐mediated calcium responses by phenytoin through the suppression of calcium excretion in human gingival fibroblasts. (4th January 2023)

• Record Type: Journal Article
• Authors: Minowa, Erika; Hayashi, Yoshinobu; Goh, Kenji; Ishida, Narumi; Kurashige, Yoshihito; Nezu, Akihiro; Saitoh, Masato; Tanimura, Akihiko
• Is Part Of: Journal of periodontal research. Volume 58:Number 2(2023)
• Page Start: 274
• Page End: 282
• Publication Date: 2023-01-04
• Subjects: calcium signaling -- fluorescence imaging -- gingival overgrowth -- human gingival fibroblasts; Periodontics -- Periodicals; 617.632
• DOI: 10.1111/jre.13089
• Languages: English
• ISSNs: 0022-3484

Abstract

Abstract: Background and Objectives: Gingival overgrowth caused by phenytoin is proposed to be associated with Ca 2+ signaling; however, the mechanisms that increase the intracellular Ca 2+ concentration ([Ca 2+ ]i ) are controversial. The current study aimed to elucidate the mechanism underlying the phenytoin‐induced increase in [Ca 2+ ]i in human gingival fibroblasts (HGFs). Methods: Effects of 100 μM phenytoin on [Ca 2+ ]i in HGFs were examined at the single‐cell level using fluorescence images of fura‐2 captured by an imaging system consisting of an EM‐CCD camera coupled to an inverted fluorescence microscope at room temperature. Results: Exposure of HGFs to 100 μM phenytoin induced a transient increase in [Ca 2+ ]i in the absence of extracellular Ca 2+, indicating that the phenytoin‐induced increase in [Ca 2+ ]i does not require an influx of extracellular Ca 2+ . In addition, phenytoin increased [Ca 2+ ]i in HGFs depleted of intracellular Ca 2+ stores by thapsigargin, indicating that neither Ca 2+ release from stores nor inhibition of Ca 2+ uptake is involved. Furthermore, the phenytoin‐induced [Ca 2+ ]i elevation was reduced to 18.8% in the absence of extracellular Na +, and [Ca 2+ ]i elevation upon removal of extracellular Na + was reduced to 25.9% in the presence of phenytoin. These results imply that phenytoin increases [Ca 2+ ]i of HGFs by suppressing the Na + /Ca 2+ exchanger. Suppression of intracellular Ca 2+ excretion is thought to enhance the Ca 2+ responses induced by various stimuli. Analysis at the single‐cell level showed that stimulation with 1 μM ATP or 3 μM histamine increased [Ca 2+ ]i in 20–50% of cells, and [Ca 2+ ]i increased in many unresponsive cells in the presence of phenytoin. Conclusion: Our findings demonstrate that phenytoin induced increase in [Ca 2+ ]i by the inhibition of Ca 2+ efflux in HGFs. It was also found that phenytoin strongly enhanced small Ca 2+ responses induced by stimulation with a low concentration of ATP or histamine by inhibiting Ca 2+ efflux. These findings suggest a possibility that phenytoin causes drug‐induced gingival overgrowth by interacting with inflammatory bioactive substances in the gingiva.