L-AP4 inhibition of depolarization-evoked cGMP formation in rat cerebellum

Neurosci Lett. 1997 Jun 13;228(3):191-4. doi: 10.1016/s0304-3940(97)00402-3.

Abstract

The effects of the group III mGluR agonist, L-2-amino-4-phosphonobutyrate (L-AP4), on depolarization-stimulated cGMP levels in adult rat cerebellar slices were determined. L-AP4 elicited a concentration-dependent, complete inhibition of cGMP formation stimulated by 4-aminopyridine (4-AP; 1 mM), yielding an IC50 value of 4.2 +/- 1.6 microM (n = 3). The 4-AP response was also reduced by the P-type Ca2+ channel toxins omega-conotoxin MVIIC (3 microM; 39 +/- 7% inhibition) and omega-Agatoxin IVA (30 nM; 53 +/- 4%), and was abolished in the absence of Ca2+ or in the presence of Co2+. The inhibitions of the 4-AP cGMP response by 10 microM L-AP4 and 30 nM omega-Agatoxin IVA were not additive, indicating that part of the actions of L-AP4 in the cerebellum involves the modulation of P-type Ca2+ channels.

MeSH terms

  • 4-Aminopyridine / pharmacology
  • Aminobutyrates / pharmacology*
  • Animals
  • CHO Cells
  • Calcium Channel Blockers / pharmacology
  • Cerebellum / drug effects
  • Cerebellum / metabolism*
  • Cricetinae
  • Cyclic GMP / biosynthesis*
  • Excitatory Amino Acid Antagonists / pharmacology*
  • In Vitro Techniques
  • Male
  • Nitroprusside / pharmacology
  • Peptides / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Spider Venoms / pharmacology
  • Vasodilator Agents / pharmacology
  • omega-Agatoxin IVA
  • omega-Conotoxins*

Substances

  • Aminobutyrates
  • Calcium Channel Blockers
  • Excitatory Amino Acid Antagonists
  • Peptides
  • Spider Venoms
  • Vasodilator Agents
  • omega-Agatoxin IVA
  • omega-Conotoxins
  • omega-conotoxin-MVIIC
  • Nitroprusside
  • 4-Aminopyridine
  • Cyclic GMP
  • 2-amino-4-phosphonobutyric acid