Release of [3H]acetylcholine from the isolated rat or guinea-pig trachea evoked by preganglionic nerve stimulation; a comparison with transmural stimulation

Author(s):  
I. Wessler ◽  
A. Klein ◽  
D. Pohan ◽  
J. Maclagana ◽  
K. Rack�

1970 ◽  
Vol 174 (1037) ◽  
pp. 503-515 ◽  

A simplified apparatus for the perfusion of the isolated rat liver is described. The operative technique has been developed so as to avoid any interruption in the blood supply to the liver. By the generally accepted criteria of viability the liver remains almost normal for up to 4 h. Perfusion with oxygenated blood through both the hepatic artery and portal vein confers no special advantages over portal perfusion alone, as judged by lactate utilization. No overflows of sympathetic transmitter could be detected from the perfused liver of the rat after nerve stimulation unless catechol- O -methyl transferase inhibitors were present; even in the presence of phenoxybenzamine (to block transmitter uptake by nerve endings) overflows were small. Larger transmitter overflows were obtained from the perfused liver of guinea-pig. Nerve stimulation caused a transient increase in the rate of gluconeogenesis by the rat liver; the maximum response, an increase of 60 %, occurred after 5 min stimulation at a frequency of 10 Hz.



1969 ◽  
Vol 47 (2) ◽  
pp. 185-192 ◽  
Author(s):  
Marvin M. Goldenberg

A close structural analogue of hemicholinium, α,α′-bis(dimethylammoniumacetaldehyde diethylacetal)-p,p′-diacetylbiphenyl bromide (DMAE), was reported to antagonize responses to ganglionic stimulants more than responses to preganglionic nerve stimulation in the cat or dog and to possess activity both similar to and different from cocaine. The present study was concerned with the effect of DMAE and atropine on the response of the isolated guinea pig ileum to ganglionic stimulants and to transmural stimulation. Nicotine and DMPP, ganglionic stimulants, caused initial spike-like contraction, which was blocked by atropine, followed by a slow sustained contraction, which was atropine-resistant but was inhibited by DMAE. Cocaine and morphine, unlike DMAE, did not elicit a differential antagonism of the biphasic effects of the ganglionic stimulants. Contractions evoked by transmural stimulation were, however, augmented by DMAE but reduced by cocaine and atropine. DMAE could induce contractions of the ileum, by means of intrinsic excitation of the cholinergic neuronal elements and not by a direct action on cholinergic smooth muscle receptors. In conclusion, ganglionic stimulants have revealed in the guinea pig ileum an atropine-resistant noncholinergic neuronal pathway which was sensitive to DMAE blockade. Furthermore, actions of DMAE and cocaine on contractions caused by ganglionic stimulants and transmural stimulation were found to be nonparallel.



1987 ◽  
Vol 134 (1) ◽  
pp. 77-82 ◽  
Author(s):  
Toku Takahashi ◽  
Masato Kusunoki ◽  
Yoshio Ishikawa ◽  
Masaru Kantoh ◽  
Takehira Yamamura ◽  
...  






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