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Important modifications by sugammadex, a modified γ-cyclodextrin, of ion currents in differentiated NSC-34 neuronal cells.
Hsu, Hung-Te; Lo, Yi-Ching; Huang, Yan-Ming; Tseng, Yu-Ting; Wu, Sheng-Nan.
Afiliação
  • Hsu HT; Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung City, 80708, Taiwan.
  • Lo YC; Department of Anesthesia, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung City, 80145, Taiwan.
  • Huang YM; Department of Pharmacology, School of Medicine, Kaohsiung Medical University, Kaohsiung City, 80708, Taiwan. yichlo@kmu.edu.tw.
  • Tseng YT; Department of Physiology, National Cheng Kung University Medical College, No. 1, University Road, Tainan City, 70101, Taiwan.
  • Wu SN; Department of Pharmacology, School of Medicine, Kaohsiung Medical University, Kaohsiung City, 80708, Taiwan.
BMC Neurosci ; 18(1): 6, 2017 01 03.
Article em En | MEDLINE | ID: mdl-28049438
ABSTRACT

BACKGROUND:

Sugammadex (SGX) is a modified γ-cyclodextrin used for reversal of steroidal neuromuscular blocking agents during general anesthesia. Despite its application in clinical use, whether SGX treatment exerts any effects on membrane ion currents in neurons remains largely unclear. In this study, effects of SGX treatment on ion currents, particularly on delayed-rectifier K+ current [I K(DR)], were extensively investigated in differentiated NSC-34 neuronal cells.

RESULTS:

After cells were exposed to SGX (30 µM), there was a reduction in the amplitude of I K(DR) followed by an apparent slowing in current activation in response to membrane depolarization. The challenge of cells with SGX produced a depolarized shift by 15 mV in the activation curve of I K(DR) accompanied by increased gating charge of this current. However, the inactivation curve of I K(DR) remained unchanged following SGX treatment, as compared with that in untreated cells. According to a minimal reaction scheme, the lengthening of activation time constant of I K(DR) caused by cell treatment with different SGX concentrations was quantitatively estimated with a dissociation constant of 17.5 µM, a value that is clinically achievable. Accumulative slowing in I K(DR) activation elicited by repetitive stimuli was enhanced in SGX-treated cells. SGX treatment did not alter the amplitude of voltage-gated Na+ currents. In SGX-treated cells, dexamethasone (30 µM), a synthetic glucocorticoid, produced little or no effect on L-type Ca2+ currents, although it effectively suppressed the amplitude of this current in untreated cells.

CONCLUSIONS:

The treatment of SGX may influence the amplitude and gating of I K(DR) and its actions could potentially contribute to functional activities of motor neurons if similar results were found in vivo.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gama-Ciclodextrinas / Canais de Potássio de Retificação Tardia / Potenciais da Membrana / Neurônios Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gama-Ciclodextrinas / Canais de Potássio de Retificação Tardia / Potenciais da Membrana / Neurônios Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article