Carbamazepine distinguishes between adenosine receptors that mediate different second messenger responses

This publication has 36 references indexed in Scilit:

• Carbamazepine, but not caffeine, is highly selective for adenosine A1 binding sites
  European Journal of Pharmacology, 1989
• A neuroglial cooperativity is required for the potentiation by 2- chloroadenosine of the muscarinic-sensitive phospholipase C in the striatum
  Journal of Neuroscience, 1989
• Long-term lithium treatment selectively reduces receptor-coupled inositol phospholipid hydrolysis in rat brain
  Biological Psychiatry, 1989
• Upregulation of Adenosine Al Receptors and Forskolin Binding Sites Following Chronic Treatment with Caffeine or Carbamazepine: A Quantitative Autoradiographic Study
  Epilepsia, 1989
• Lithium modulation of second messenger signal amplification in man: Inhibition of phosphatidylinositol- specific phospholipase C and adenylate cyclase activity
  Psychiatry Research, 1988
• Non-xanthine heterocycles: Activity as antagonists of A1 and A2-adenosine receptors
  Biochemical Pharmacology, 1988
• Common modes of drug action on Na+ channels: local anesthetics, antiarrhythmics and anticonvulsants
  Trends in Pharmacological Sciences, 1987
• Secretagogue-induced phosphoinositide metabolism in human leucocytes
  Biochemical Journal, 1984
• [9] Separation of lymphocytes, granulocytes, and monocytes from human blood using iodinated density gradient media
  Published by Elsevier ,1984
• Subclasses of adenosine receptors in the central nervous system: Interaction with caffeine and related methylxanthines
  Cellular and Molecular Neurobiology, 1983