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DOI 10.1016/j.bbrc.2022.07.038

Медицинская библиотека · Biochemical and biophysical research communications · 2022

Dantrolene reduces platelet-derived growth factor (PDGF)-induced vascular smooth muscle cell proliferation and neointimal formation following vascular injury in mice.

Sakai Chihiro, Mikawa Mei, Yamamoto Takeshi, Uchida Tomoyuki, Nakamura Yoshihide, Akase Hideaki, Suetomi Takeshi, Tominaga Naoomi, Inamitsu Masako, Oda Tetsuro, Okamura Takayuki, Kobayashi Shigeki, Yano Masafumi

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Аннотация

Dantrolene is a ryanodine receptor blocker that is used clinically for treatment of malignant hyperthermia. This study was conducted using murine aortic vascular smooth muscle cells (MOVAS) and a mouse arterial injury model to investigate the inhibitory effect of dantrolene on smooth muscle cell proliferation and migration. We investigated whether dantrolene suppressed platelet-derived growth factor (PDGF)-induced vascular smooth muscle cell proliferation and migration in vitro. The effect of dantrolene on smooth muscle phenotype was evaluated using immunostaining. In addition, smooth muscle cell proliferation and phenotype switching were tested by applying dantrolene around blood vessels using a mouse arterial injury model. Dantrolene inhibited PDGF-induced cell proliferation and migration of MOVAS. Dantrolene also inhibited the switch from contractile to synthetic phenotype both in vitro and in vivo. Dantrolene is effective at inhibiting vascular smooth muscle cell proliferation, migration, and neointimal formation following arterial injury in mice.

Для цитирования: Sakai Chihiro, Mikawa Mei, Yamamoto Takeshi, Uchida Tomoyuki, Nakamura Yoshihide, Akase Hideaki, Suetomi Takeshi, Tominaga Naoomi, Inamitsu Masako, Oda Tetsuro, Okamura Takayuki, Kobayashi Shigeki, Yano Masafumi. Dantrolene reduces platelet-derived growth factor (PDGF)-induced vascular smooth muscle cell proliferation and neointimal formation following vascular injury in mice.. Biochemical and biophysical research communications. 2022. DOI: 10.1016/j.bbrc.2022.07.038.

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