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Activation of CCK-B receptors elevates cytosolic Ca2+ levels in a pituitary cell line.
Kuwahara, T; Nagase, H; Takamiya, M; Yoshizaki, H; Kudoh, T; Nakano, A; Arisawa, M.
Afiliación
  • Kuwahara T; Department of Pharmaceutical Screening, Nippon Roche Research Center, Kamakura, Japan.
Peptides ; 14(4): 801-5, 1993.
Article en En | MEDLINE | ID: mdl-8234029
ABSTRACT
Cytosolic Ca2+ levels ([Ca2+]i) in GH3 cells, a rat anterior pituitary tumor cell line, were monitored with fura-2 by fluorescence measurements. Cholecystokinin octapeptide (CCK-8) produced a transient elevation of [Ca2+]i. The elevation of [Ca2+]i by CCK-8 was inhibited by L-365,260, but not by devazepide. It was still observed when extracellular Ca2+ was eliminated, indicating that CCK-8 mobilizes Ca2+ from intracellular storage sites after interaction with CCK-B receptors. Cholecystokinin octapeptide increased the turnover of phosphatidylinositol, but it did not affect cyclic AMP levels. A possible involvement of phosphatidylinositol breakdown and calcium mobilization in the transduction system of CCK-B receptors in GH3 cells is suggested.
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Bases de datos: MEDLINE Asunto principal: Adenohipófisis / Calcio / Receptores de Colecistoquinina / Citosol Límite: Animals Idioma: En Revista: Peptides Año: 1993 Tipo del documento: Article País de afiliación: Japón
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Bases de datos: MEDLINE Asunto principal: Adenohipófisis / Calcio / Receptores de Colecistoquinina / Citosol Límite: Animals Idioma: En Revista: Peptides Año: 1993 Tipo del documento: Article País de afiliación: Japón