Alteration of Ethanol Preference in Hamsters: Effects of Photoperiod and 5-Hydroxytryptophan

Author(s):  
Irving Geller ◽  
Roy J. Hartmann
Keyword(s):  
2017 ◽  
Vol 475 (1) ◽  
pp. 148-150 ◽  
Author(s):  
M. V. Dorofeikova ◽  
A. Yu. Egorov ◽  
E. V. Filatova ◽  
A. A. Orlov
Keyword(s):  

2021 ◽  
pp. 114865
Author(s):  
Bruno Gianfratti ◽  
Ricardo Tabach ◽  
Marna Eliana Sakalem ◽  
Talita Stessuk ◽  
Lucas Oliveira Maia ◽  
...  

Author(s):  
Isadora Marques Paiva ◽  
Luana Martins de Carvalho ◽  
Isabela Martins Di Chiaccio ◽  
Isadora de Lima Assis ◽  
Elena Sánchez Naranjo ◽  
...  

2009 ◽  
Vol 31 (5) ◽  
pp. 291-302 ◽  
Author(s):  
Sarah K. Williams ◽  
Elizabeth T. Cox ◽  
Matthew S. McMurray ◽  
Emily E. Fay ◽  
Thomas M. Jarrett ◽  
...  

2020 ◽  
Vol 223 (11) ◽  
pp. jeb224121
Author(s):  
Scarlet J. Park ◽  
William W. Ja

2011 ◽  
Vol 106 (6) ◽  
pp. 3145-3156 ◽  
Author(s):  
Christian H. Lemon ◽  
David M. Wilson ◽  
Susan M. Brasser

In randomly bred rats, orally applied ethanol stimulates neural substrates for appetitive sweet taste. To study associations between ethanol's oral sensory characteristics and genetically mediated ethanol preference, we made electrophysiological recordings of oral responses (spike density) by taste-sensitive nucleus tractus solitarii neurons in anesthetized selectively bred ethanol-preferring (P) rats and their genetically heterogeneous Wistar (W) control strain. Stimuli (25 total) included ethanol [3%, 5%, 10%, 15%, 25%, and 40% (vol/vol)], a sucrose series (0.01, 0.03, 0.1, 0.3, 0.5, and 1 M), and other sweet, salt, acidic, and bitter stimuli; 50 P and 39 W neurons were sampled. k-means clustering applied to the sucrose response series identified cells showing high (S1) or relatively low (S0) sensitivity to sucrose. A three-way factorial analysis revealed that activity to ethanol was influenced by a neuron's sensitivity to sucrose, ethanol concentration, and rat line ( P = 0.01). Ethanol produced concentration-dependent responses in S1 neurons that were larger than those in S0 cells. Although responses to ethanol by S1 cells did not differ between lines, neuronal firing rates to ethanol in S0 cells increased across concentration only in P rats. Correlation and multivariate analyses revealed that ethanol evoked responses in W neurons that were strongly and selectively associated with activity to sweet stimuli, whereas responses to ethanol by P neurons were not easily associated with activity to representative sweet, sodium salt, acidic, or bitter stimuli. These findings show differential central neural representation of oral ethanol between genetically heterogeneous rats and P rats genetically selected to prefer alcohol.


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