PharmacyPharmacologyToxicologyNeurochemistryNeuropharmacologyNeurotoxicologyCentral Nervous System ToxicityHepatic EncephalopathyHepatotoxicity MechanismsNeurotoxic MechanismsNeurotoxicity MechanismsAcute Central Nervous System ToxicityAlterationBrain ToxicityHypertonicityMuscle HypertonicityRodent NeurotoxicologyToxic EncephalopathyTryptophan Metabolism
In a previous paper we have reported that the oral long-term administration of 200 mg/kd of L-tryptophan to rats with a porto-caval shunt causes significant loss of body weight, muscular hypertonicity and aggressivity, as well as marked alteration of the liver structure. We now report that tryptophan administered at the same dosage for the same length of time also induces significant alteration of the central nervous system. These results further demonstrate that high plasma levels of tryptophan are quite well tolerated by control animals but are quite toxic to rats with a porto-caval shunt. We also claim that the brain alterations observed in such animals are not secondary to liver dysfunction but to high levels of plasma tryptophan per se.
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William V. McDermott, Raymond D. Adams, A G Riddell · Annals of Surgery · 1954 · 144 citations
URINARY AND SERUM OCTOPAMINE IN PATIENTS WITH PORTAL-SYSTEMIC ENCEPHALOPATHY
KishuK. Manghani, MichaelR. Lunzer, BarbaraH. Billing et al. · The Lancet · 1975 · 88 citations