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Ion channel modulation as the basis for neuroprotective action of MS-153
- Uenishi, Hiroak;
- Huang, Chao-Sheng;
- Song, Jin-Ho;
- Marszalec, William;
- Narahashi, Toshio
WEB OF SCIENCE
12SCOPUS
12초록
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
- 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
- 발행일
- 1999
- 유형
- Article; Proceedings Paper
- 권
- 890
- 페이지
- 385 ~ 399
- 언어
- ENG
- 출판사
- NEW YORK ACAD SCIENCES
- 발행국가
- 미국
- 분량
- 15 페이지
- ISSN
- E 1749-6632
P 0077-8923