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Potentiation of motoneurone excitability by combined administration of 5-HT agonist and TRH analogue.

K A Clarke, A J Parker, G C Stirk

Neuropeptides June 1, 1985 DOI: 10.1016/0143-4179(85)90098-8 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Rats anaesthetised with urethane
Interventions RX77368 5MeODMT
Dose RX77368 1 mg/kg; 5MeODMT 0.4 mg/kg
Citations 39
Key findings Combined administration of RX77368 and 5MeODMT potentiated the increase in amplitude and duration of motoneurone field potentials compared to either drug alone.

Abstract

Motoneurone field potentials have been recorded from the lumbar region of the spinal cord, to antidromic stimulation of a ventral root, in rats anaesthetised with urethane. Injection of the thyrotropin releasing hormone (TRH) analogue RX77368 (1mg/kg) plus the 5-hydroxytryptamine (5-HT) receptor agonist 5-methoxy-N, N-dimethyl-tryptamine (5MeODMT 0.4mg/kg) resulted in a potentiation of the increase in amplitude and duration of response, compared to when the drugs were given singly. These results are discussed in the context of possible interactions between 5-HT and TRH systems.