1989
DOI: 10.1254/jjp.50.511
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Effect of /-ephedrine on cholinergic neurotransmission in the isolated guinea pig ileum.

Abstract: Abstract-In the isolated guinea pig ileum, the effects of /-ephedrine on the twitch response to field stimulation were investigated in the presence of propranolol. Ephedrine and clonidine inhibited the twitch response but not the contraction to exogenous acetylcholine. The inhibitory effect of clonidine was significantly diminished by yohimbine pretreatment. However, the inhibitory effect of ephedrine was not influenced by yohimbine, sulpiride or 6-hydroxydopamine (6-OHDA) pretreatment. Most of this action of … Show more

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“…Cyclizations of the chiral iminium salt (4) with base afforded the carbinolamine ether (5) reduction of which with benzylic cleavage yielded (6, R = H). 13 The cyclization of the vinyl sulphoxides (7) and (8), obtained by Wittig reaction from the corresponding aldehyde, was achieved by base, when the 2isomer (7) gave the tetrahydroisoquinoline (9) and the E-isomer (8) yielded the enantiomer of (9). Desulphurizing reduction of (9) yielded 5-( -)-carnegine (6, R = Me) and desulphurization of its enantiomer gave R-( +)-carnegine.I4 Mescaline and homoveratrylamine have been converted by Pictet-Spengler cyclization with the masked aldehydes (10) and ( I I ) respectively into anhalinine (12, R1 = OMe, R2 = H)15 and calycotomine (12, R1 = H, R2 = CH20H).…”
Section: Lsoquinolinesmentioning
confidence: 99%
“…Cyclizations of the chiral iminium salt (4) with base afforded the carbinolamine ether (5) reduction of which with benzylic cleavage yielded (6, R = H). 13 The cyclization of the vinyl sulphoxides (7) and (8), obtained by Wittig reaction from the corresponding aldehyde, was achieved by base, when the 2isomer (7) gave the tetrahydroisoquinoline (9) and the E-isomer (8) yielded the enantiomer of (9). Desulphurizing reduction of (9) yielded 5-( -)-carnegine (6, R = Me) and desulphurization of its enantiomer gave R-( +)-carnegine.I4 Mescaline and homoveratrylamine have been converted by Pictet-Spengler cyclization with the masked aldehydes (10) and ( I I ) respectively into anhalinine (12, R1 = OMe, R2 = H)15 and calycotomine (12, R1 = H, R2 = CH20H).…”
Section: Lsoquinolinesmentioning
confidence: 99%