Initiation of Ethanol Reinforcement using a Sucrose-Substitution Procedure in Food- and Water-Sated Rats

1986 ◽  
Vol 10 (4) ◽  
pp. 436-442 ◽  
Author(s):  
Herman H. Samson
2019 ◽  
Vol 22 (2) ◽  
pp. 238-247 ◽  
Author(s):  
Scott T Barrett ◽  
Brady M Thompson ◽  
Jessica R Emory ◽  
Chris E Larsen ◽  
Steven T Pittenger ◽  
...  

Abstract Background Alcohol is often consumed with tobacco, and dependence to alcohol and tobacco are highly comorbid. In addition, there are differences in the prevalence of nicotine- and alcohol-abuse between the sexes. Nicotine produces enhancing effects on the value of other reinforcers, which may extend to alcohol. Methods Male and female Wistar rats were trained to self-administer 15% ethanol solution in 30-minute sessions. Once ethanol self-administration was established, demand for ethanol was evaluated using an exponential reinforcer demand method, in which the response cost per reinforcer delivery was systematically increased over blocks of several sessions. Within each cost condition, rats were preinjected with nicotine (0.05, 0.1, 0.2, or 0.4 mg/kg base, SC) or saline 5 minutes before self-administration sessions. The effects of nicotine dose and biological sex were evaluated using the estimates generated by the reinforcer demand model. Results Under saline conditions, males showed greater sensitivity to ethanol reinforcement than females. Nicotine enhanced the reinforcement value of alcohol and this varied with sex. In both sexes, 0.4 mg/kg nicotine decreased intensity of ethanol demand. However, 0.05, 0.1, and 0.2 mg/kg nicotine decreased elasticity of ethanol demand in females, but not in males. Conclusions Nicotine enhances ethanol reinforcement, which may partially drive comorbidity between nicotine-abuse and alcohol-abuse. Males showed signs of greater ethanol reinforcement value than females under saline conditions, and nicotine attenuated this effect by increasing ethanol reinforcement value in the females. These findings highlight that a complete understanding of alcohol-abuse must include a thorough study of alcohol use in the context of other drug use, including nicotine. Implications Nicotine dose dependently enhances the alcohol reinforcement value in a manner that is clearly influenced by biological sex. Under saline baseline conditions, males show lower elasticity of demand for alcohol reinforcement than females, indicative of greater reinforcement value. However, nicotine attenuated this difference by enhancing alcohol reward in the females. Specifically, low-to-moderate doses (0.05–0.2 mg/kg) of nicotine decreased elasticity of alcohol demand in female rats, increasing the perseverance of their alcohol taking behavior. These data indicate that the well-documented reward-enhancing effects of nicotine on sensory reinforcement extend to alcohol reinforcement and that these vary with biological sex.


2012 ◽  
Vol 226 (3) ◽  
pp. 491-499 ◽  
Author(s):  
Samanta M. March ◽  
Paula Abate ◽  
Norman E. Spear ◽  
Juan Carlos Molina

1963 ◽  
Vol 30 (3) ◽  
pp. 415-418 ◽  
Author(s):  
M. H. Cobble ◽  
W. F. Ames

A classical substitution procedure for solving Poisson’s equation ∇2φ = −K is extended by application of certain coordinate transformations suggested by the functional form of K. The method is applied to the determination of fluid-velocity fields in two curvilinear geometries.


1992 ◽  
Vol 654 (1 The Neurobiol) ◽  
pp. 61-69 ◽  
Author(s):  
R. ADRON HARRIS ◽  
MARK S. BRODIE ◽  
THOMAS V. DUNWIDDIE

1978 ◽  
Vol 87 (6) ◽  
pp. 772-777 ◽  
Author(s):  
Derald E. Brackmann ◽  
William E. Hitselberger ◽  
Jerald V. Robinson

Facial nerve continuity was restored during cerebellopontine angle tumor removal in nine cases. The distal facial nerve was rerouted from the stylomastoid foramen into the cerebellopontine angle. Direct suture was accomplished in seven cases while two required interposition of a greater auricular nerve graft. There was excellent return of facial function in eight of the nine cases. Overall results are superior to nerve substitution techniques. The facial nerve should be inspected for continuity following tumor removal. If one is not certain the nerve is intact, the proximal facial stump should be identified at the brain stem and facial nerve continuity reestablished. A nerve substitution procedure should be resorted to at a later time only when the proximal facial stump is not identifiable.


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