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Effects of Vasoactive Intestinal Polypeptide on Neurones of the Rat Suprachiasmatic Nuclei In Vitro
Effects of a blood vessel–relaxing peptide on rat brain cells that control daily rhythms
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Abstract
Approximately 50% of rat SCN neurones respond to vasoactive intestinal polypeptide (VIP).
- The primary response to VIP in SCN neurones is a suppression of spontaneous firing rate, while a minority of cells exhibit activation.
- Responses to VIP are mimicked by the VPAC(2) receptor agonist Ro 25-1553 and blocked by the selective VPAC(2) receptor antagonist PG 99-465.
- Activation of SCN cells occurs in response to the PAC(1) receptor agonist maxadilan, with 40% of cells responding.
- Responses to VIP are not influenced by antagonists targeting ionotropic glutamate receptors.
- The duration of VIP-induced suppression in firing rate is affected by the GABA(A) receptor antagonist bicuculline.
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