Endothelin-1 has been identified as a potential mediator in the pathogenesis of ischaemic stroke and cerebral vasospasm. The aim of this study was to analyse the role of voltage-operated calcium channels (VOCC) and non-VOCC in endothelin-1 induced vasoconstriction of rat cerebral arteries. Arterial segments were dissected from different regions of the cerebral circulation and responses assessed using wire myography. Endothelin-1 concentration-contraction curves were constructed in calcium-free medium or in the presence of nifedipine, NNC 55-0396 ((1S,2S)-2-(2-(N-[(3-benzimidazol-2-yl)propyl]-N-methylamino)ethyl)-6-fluoro-1,2,3,4-tetrahydro-1-isopropyl-2-naphtyl cyclopropanecarboxylate dihydrochloride) or SK&F 96365 (1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1H-imidazole) to inhibit the L-type VOCC, T-type VOCC and non-VOCC, respectively. Inhibition of the calcium channels or removal of calcium from the medium variably decreased the maximum effects (E-max) of endothelin-1, however its potency (pEC(50)) was unaltered. Endothelin-1 caused a small contraction ( <22%) in calcium-free solution. Pre-treatment with nifedipine (1 mu M) did not affect responses to low concentrations of endothelin-1 but decreased E-max, while NNC 55-0396 (1 mu M) and SK&F 96365 (30-100 mu M) generally attenuated the endothelin-1-induced contraction. Combination of nifedipine with SK&F 96365 further decreased the E-max. The relaxant effect of the calcium channel antagonists was also assessed in pre-contracted arteries. Only nifedipine and SK&F 96365 relaxed the arteries pre-contracted with endothelin-1. In conclusion, VOCC and non-VOCC calcium channels are involved in different phases of the endothelin-1 contraction in rat cerebral vessels. T-type VOCC may be involved in contraction induced by low concentrations of endothelin-1, while L-type VOCC mediate the maintenance phase of contraction. VOCC and non-VOCC may work in concert in mediating contraction induced by endothelin-1. (C) 2014 Elsevier B.V. All rights reserved.
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USP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, BrazilUSP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, Brazil
Callera, GE
Bendhack, LM
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USP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, BrazilUSP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, Brazil
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Furukawa, Taiji
Nukada, Toshihide
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Tokyo Inst Psychiat, Dept Neuronal Signaling, Tokyo, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Nukada, Toshihide
Nalmiki, Yoshiko
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Tokyo Inst Psychiat, Dept Neuronal Signaling, Tokyo, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Nalmiki, Yoshiko
Miyashita, Yoriko
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Tokyo Inst Psychiat, Dept Neuronal Signaling, Tokyo, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Miyashita, Yoriko
Hatsuno, Kento
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Hatsuno, Kento
Ueno, Yasunari
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Ueno, Yasunari
Yamakawa, Takeshi
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Yamakawa, Takeshi
Isshiki, Takaaki
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
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USP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, BrazilUSP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, Brazil
Callera, GE
Bendhack, LM
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USP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, BrazilUSP, Fac Ciencias Farmaceut, Farmacol Lab, BR-14040903 Ribeirao Preto, Brazil
机构:
Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Furukawa, Taiji
Nukada, Toshihide
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Tokyo Inst Psychiat, Dept Neuronal Signaling, Tokyo, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Nukada, Toshihide
Nalmiki, Yoshiko
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Tokyo Inst Psychiat, Dept Neuronal Signaling, Tokyo, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Nalmiki, Yoshiko
Miyashita, Yoriko
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Tokyo Inst Psychiat, Dept Neuronal Signaling, Tokyo, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Miyashita, Yoriko
Hatsuno, Kento
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Hatsuno, Kento
Ueno, Yasunari
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Ueno, Yasunari
Yamakawa, Takeshi
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan
Yamakawa, Takeshi
Isshiki, Takaaki
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Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, JapanTeikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 173, Japan