Sedative action of some substituted benzylamides.
Indian J Physiol Pharmacol
; 1977 Jan-Mar; 21(1): 1-10
Article
de En
| IMSEAR
| ID: sea-108557
Substituted benzylamide derivatives of amino acylamide (compound A,B,C, & D) were found to be less potent local anaesthetics than lignocaine and procaine. However, the four compounds exhibited sedation without ptosis and reduced spontaneous locomotor activity better than methaqualone. Compound A alone antagonised methylamphetamine induced hypermotor activity. The test compounds potentiated hexobarbitone induced hypnosis. Three compounds antagonised calcium induced stoppage of isolated heart of frog. Except compound C all caused a transitory fall of blood pressure in dog which was not blocked either by atropine or propranolol. These compounds showed neuromuscular blockade and possessed slight analgesic activity but were devoid of anticonvulsant and tranquillizing activity. LD 50 values were calculated to be 164.1 +/- 23.0, 229.1 +/- 51.0, 181.6 +/- 28.18 and 416+/-38.2 mg/kg for compounds A,B,C & D respectively.
Texte intégral:
1
Indice:
IMSEAR
Sujet Principal:
Anura
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Lapins
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Rats
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Composés benzyliques
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Pression sanguine
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Femelle
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Mâle
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Dépression chimique
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Chiens
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Amides
langue:
En
Texte intégral:
Indian J. physiol. pharmacol
Année:
1977
Type:
Article