The effect of two types of baseline training on behavioral contrast and the peak shift

1973 ◽  
Vol 2 (6) ◽  
pp. 407-409 ◽  
Author(s):  
Abdulaziz A. Dukhayyil ◽  
Joseph E. Lyons

1973 ◽  
Vol 32 (1) ◽  
pp. 47-58 ◽  
Author(s):  
Stephanie G. Weinberg

Rats were pretrained in the presence of an auditory click rate stimulus of 14 pps correlated with variable-interval or variable-ratio reinforcement. During subsequent discrimination training, the added stimulus, correlated with extinction, was 18, 36, 72, or 0 (no sound) pps. After discrimination, Ss were given a generalization test session, in extinction, in which five click rate stimuli were presented. The inverse relationship between physical separation of the discrimination training stimuli and amount of peak shift of the generalization gradient occurred regardless of the original positive reinforcement schedule during training. Behavioral contrast was not produced by all Ss. Results demonstrated no effect of separation of training stimuli on behavioral contrast and that behavioral contrast and peak shift need not covary.



1976 ◽  
Vol 43 (3_suppl) ◽  
pp. 1167-1175
Author(s):  
James F. Mc Coy ◽  
Merrill E. Pratt ◽  
Alan R. Benson

Three experiments examined multiple-schedule interactions in a free-operant paradigm for rats. In Exps. 1 and 2 three rats each and in Exp. 3 five rats were given extended multiple variable-interval baseline training before being shifted to multiple variable-interval extinction. Visual discriminative stimuli and regular extinction, which allowed nonreinforced responding, were used in Exps. 1 and 2, but auditory discriminative stimuli and retraction of the lever to prevent responding during extinction were used in Exp. 3. Positive behavioral contrast was observed in only one out of six rats in Exps. 1 and 2, while negative induction was observed in the other five subjects. However, contrast was observed at some point in training for all five subjects in Exp. 3. The differential multiple-schedule interactions were attributed to the introduction of an additional stimulus-reinforcer dependency with regard to the presence vs absence of the lever in Exp. 3. Results support an autoshaping or additivity account of behavioral contrast.





1980 ◽  
Vol 33 (1) ◽  
pp. 101-118 ◽  
Author(s):  
M. Catherine Bushnell ◽  
Stanley J. Weiss


2009 ◽  
Author(s):  
Matthew G. Wisniewski ◽  
Barbara A. Church ◽  
Eduardo Mercado
Keyword(s):  


2008 ◽  
Author(s):  
Matthew G. Wisniewski ◽  
Barbara A. Church ◽  
Eduardo Mercado


2020 ◽  
Vol 26 (31) ◽  
pp. 3828-3833 ◽  
Author(s):  
Tuula Peñate-Medina ◽  
Eike Kraas ◽  
Kunliang Luo ◽  
Jana Humbert ◽  
Hanwen Zhu ◽  
...  

Background: Nanoparticle imaging and tracking the release of the loaded material from the nanoparticle system have attracted significant attention in recent years. If the release of the loaded molecules could be monitored reliably in vivo, it would speed up the development of drug delivery systems remarkably. Methods: Here, we test a system that uses indocyanine green (ICG) as a fluorescent agent for studying release kinetics in vitro and in vivo from the lipid iron nanoparticle delivery system. The ICG spectral properties like its concentration dependence, sensitivity and the fluctuation of the absorption and emission wavelengths can be utilized for gathering information about the change of the ICG surrounding. Results: We have found that the absorption, fluorescence, and photoacoustic spectra of ICG in lipid iron nanoparticles differ from the spectra of ICG in pure water and plasma. We followed the ICG containing liposomal nanoparticle uptake into squamous carcinoma cells (SCC) by fluorescence microscopy and the in vivo uptake into SCC tumors in an orthotopic xenograft nude mouse model under a surgical microscope. Conclusion: Absorption and emission properties of ICG in the different solvent environment, like in plasma and human serum albumin, differ from those in aqueous solution. Photoacoustic spectral imaging confirmed a peak shift towards longer wavelengths and an intensity increase of ICG when bound to the lipids. The SCC cells showed that the ICG containing liposomes bind to the cell surface but are not internalized in the SCC-9 cells after 60 minutes of incubation. We also showed here that ICG containing liposomal nanoparticles can be traced under a surgical camera in vivo in orthotopic SCC xenografts in mice.



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