Y. Haskel et M. Hanani, INHIBITION OF GASTROINTESTINAL MOTILITY BY MPTP VIA ADRENERGIC AND DOPAMINERGIC MECHANISMS, Digestive diseases and sciences, 39(11), 1994, pp. 2364-2367
The neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrine (MPTP) was i
njected intraperitoneally in mice and caused an acute inhibition (of o
ver 60%) of gastrointestinal motility, which was measured by the trans
it of charcoal. This inhibition was not related to conversion of MPTP
to MPP(+). Administration of the beta-adrenergic blocker propranolol s
ignificantly reduced, but did not completely block, the effect of MPTP
. The dopaminergic blocker haloperidol also partly reversed the effect
s of MPTP. When these blockers were administered together, the action
of MPTP was fully blocked. The results indicate that the toxin acted b
y releasing catecholamines (presumably norepinephrine and dopamine), t
hereby inhibiting motility.