Ion channel modulation as the basis for neuroprotective action of MS-153

  • Uenishi, Hiroak; 
  • Huang, Chao-Sheng; 
  • Song, Jin-Ho; 
  • Marszalec, William; 
  • Narahashi, Toshio
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초록

MS-153, (R)-(-)-5-methyl-1-nicotinoyl-2-pyrazoline is a new neuroprotective drug, Recent data in the literature suggest that it inhibits glutamate accumulation occurring during ischemia and the translocation of protein kinase C gamma (PKC gamma). The present study was undertaken to prove the hypothesis that MS-153 blocks neuroreceptors and ion channels involved in glutamate accumulation. Neurons isolated from rat dorsal root ganglia and frontal cortex were used for recording channel currents by the whole-cell patch clamp technique. The effects of bath-applied MS-153 were examined on: tetrodotoxin-sensitive and tetrodotoxin-resistant sodium channels and high voltage-gated calcium channels of dorsal root ganglion neurons, and channels activated by glutamate, N-methyl-D-aspartate (NMDA), kainate, alpha-amino-3-hydroxy-5methyl- 4-isoxarole propionic acid (AMPA), gamma-aminobutyric acid (GABA) and acetylcholine (ACh) in cortical neurons. MS-153 at a concentration of 300 mu M had no effect on either:tetrodotoxin-sensitive or tetrodotoxin-resistant sodium channels. High voltage-gated calcium channels were either suppressed or not affected by 1-300 mu M MS-153. The variable blocking effect of MS-153 was due to the variable activity of intracellular components in individual neurons, especially that of PKC, whose translocation is known to be inhibited by MS-153. When 100 nM phorbol 12-myristate-13-acetate (PMA) was applied to neurons, MS-153 suppressed the calcium channel current more frequently. Calphostin C (0.5 mu M), a specific PKC inhibitor, applied intracellularly via recording patch pipette, completely abolished MS-153 suppression of the calcium channel current. Currents induced by glutamate, NMDA, kainate, AMPA, GABA or ACh were not affected by MS-153 at 300 mu M. It was concluded that MS-153 inhibited high voltage-gated calcium channels through interactions with PKC, thereby preventing massive release of glutamate from nerve terminals in ischemic conditions.

키워드

ACTIVATED CALCIUM CHANNELS; ROOT GANGLION NEURONS; RESISTANT SODIUM-CHANNELS; CA2+ CHANNELS; SENSORY NEURONS; CYCLIC-AMP; RAT; RILUZOLE; CURRENTS; INHIBITION
제목
Ion channel modulation as the basis for neuroprotective action of MS-153
저자
Uenishi, Hiroak; Huang, Chao-Sheng; Song, Jin-Ho; Marszalec, William; Narahashi, Toshio
DOI
10.1111/j.1749-6632.1999.tb08018.x
발행일
1999
유형
Article; Proceedings Paper
저널명
Annals of the New York Academy of Sciences
권
890
페이지
385 ~ 399