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dc.contributor.authorGuantai Anastacia N.
dc.contributor.authorMwangi, J.W
dc.contributor.authorMuriuki, Gichuru
dc.contributor.authorKuria, K.A.M.
dc.date.accessioned2013-02-25T06:34:05Z
dc.date.issued1986
dc.identifier.citationNeuropharmacology Vol.26 No.5 pp 410-405,1987en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/11035
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/3037411
dc.description.abstract-( - )-Cathinone and d-norpseudoephedrine (ONE) in the dose range 0.2-1.2 mg/ml produced a reduction in contractions of skeletal muscle, evoked by direct and indirect electrical stimulation and antagonised the facilitatory action of physostigmine on the neuromuscular junction; but failed to antagonise a partial blockade induced by d-tubocurarine (dTb) as occurs with norepinephrine or epinephrine. The local anaesthetic actions of ( - )-cathinone and ONE were found to be almost equivalent to that of lignocaine. These results indicate that (- )-cathinone and ONE may have a direct blocking action on the neuromuscular junction, which is independent of cholinergic and adrenergic transmission.en
dc.language.isoenen
dc.subjectCatha edulis,en
dc.subjectActive constituents,en
dc.subjectNeuromuscular junction.en
dc.titleEffects of the active constituents of catha edulis on the neuromuscular junctionen
dc.typeArticleen
local.embargo.terms6 monthsen
local.publisherMitishamba Drug Research Centre, Department of Pharmacy, College of Health Sciences, University of Nairobi,en


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