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Organogermanium compound, Ge-132, forms complexes with adrenaline, ATP and other physiological cis-diol compounds.
Nakamura, Takashi; Shimada, Yasuhiro; Takeda, Tomoya; Sato, Katsuyuki; Akiba, Mitsuo; Fukaya, Haruhiko.
Afiliación
  • Nakamura T; Asai Germanium Research Institute Co., Ltd. Suzuranoka, Hakodate, Hokkaido 042-0958, Japan.
  • Shimada Y; Asai Germanium Research Institute Co., Ltd. Suzuranoka, Hakodate, Hokkaido 042-0958, Japan.
  • Takeda T; The United Graduate School of Agricultural Science, Iwate University, Morioka, Iwate 020-8550, Japan.
  • Sato K; Asai Germanium Research Institute Co., Ltd. Suzuranoka, Hakodate, Hokkaido 042-0958, Japan.
  • Akiba M; Asai Germanium Research Institute Co., Ltd. Suzuranoka, Hakodate, Hokkaido 042-0958, Japan.
  • Fukaya H; Tokyo University of Pharmacy & Life Sciences, Horinouchi, Hachioji, Tokyo 192-0392, Japan.
Future Med Chem ; 7(10): 1233-46, 2015.
Article en En | MEDLINE | ID: mdl-26144262
BACKGROUND: In mammals, adrenaline and ATP are life-essential vicinal diol and cis-diol functional groups. Here, we show that interactions between a safe organogermanium compound and these cis-diol compounds have the potential to regulate physiological functions. In addition, we represent a possible new druggable target for controlling the action of cis-diol compounds. RESULTS: We analyzed a single crystal structure of organogermanium 3-(trihydroxygermyl)propanoic acid (THGPA), a hydrolysate of safe Ge-132, in complex with catecholamine (adrenaline and noradrenaline), and evaluated the affinity between several cis-diol compounds and THGPA by NMR. An in vitro study using normal human epidermal keratinocytes was performed to investigate the inhibition of cis-diol compound-stimulated receptors by THGPA. At high concentration, THGPA inhibited the calcium influx caused by adrenaline and ATP. CONCLUSION: This study demonstrates that THGPA can modify cis-diol-mediated cell-to-cell signaling.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos Organometálicos / Epinefrina / Adenosina Trifosfato Límite: Humans Idioma: En Revista: Future Med Chem Año: 2015 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Compuestos Organometálicos / Epinefrina / Adenosina Trifosfato Límite: Humans Idioma: En Revista: Future Med Chem Año: 2015 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido