ISSN:
1471-4159
Source:
Blackwell Publishing Journal Backfiles 1879-2005
Topics:
Medicine
Notes:
Abstract: The 29-amino-acid peptide galanin (GAL) caused concentration-dependent inhibition of the accumulation of 3H-inositol phosphates (3H-InsPs) induced by the muscarinic agonist carbachol (CARB; 10-3-10-5M) in the presence of 5 mM lithium, specifically in tissue miniprisms from rat ventral hippocampus. The inhibitory effect of GAL involved the mono-, bis-, tris-, and tetrakisphosphates formed during activation for 2 min of phospholipase C by CARB (1 mM) in the absence of lithium. GAL (1 μM) did not affect α-adrenergic or serotonergic type 2 receptor-mediated phosphoinositide (PI) breakdown in the same tissue. GAL by itself neither acted on basal levels of 3H-InsPs nor affected muscarinic receptors in binding studies. Blockade of the T-, N-, and L-types of voltage-sensitive calcium channel (VSCC) with 200 μM Cd2+ reduced muscarinic receptor-mediated PI breakdown by 50% and abolished the inhibitory effect of GAL (1 μM). Reduction of the extracellular Ca2+ concentration from 1.3 mM to 0.49 μM abolished the GAL inhibition of CARB-stimulated PI hydrolysis. Ca2+ influx promoted by 18 mM K+ depolarization or by 1 μM Bay K 8644, a selective agonist of the L-type VSCC, prevented the inhibitory effect of GAL. Blockade of the L-type VSCC with nifedipine (1 μM) potentiated the inhibitory effects of GAL without affecting muscarinic stimulation of PI breakdown. The neurotoxin ω-conotoxin (2 μM), a blocker of both L- and N-types of VSCC, by itself reduced CARB-mediated breakdown of PIs by ∼25%, and when it was added before GAL (1 μM) there was no summation of the two individual inhibitory effects, a result suggesting a common site of action for GAL and ω-conotoxin. The data presented thus indicate that GAL modulation of muscarinic stimulation of the phospholipase C activity is mediated by a reduction of Ca2+ entry through VSCCs, presumably of the N type.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1111/j.1471-4159.1991.tb01986.x
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