scholarly journals Behavioral sensitization: Characterization of enduring changes in rotational behavior produced by intermittent injections of amphetamine in male and female rats

1984 ◽  
Vol 84 (4) ◽  
pp. 466-475 ◽  
Author(s):  
Terry E. Robinson
2016 ◽  
Vol 109 ◽  
pp. 281-292 ◽  
Author(s):  
Ryan S. Poland ◽  
Yun K. Hahn ◽  
Pamela E. Knapp ◽  
Patrick M. Beardsley ◽  
M. Scott Bowers

2014 ◽  
Vol 22 (4) ◽  
pp. 356-363 ◽  
Author(s):  
Kristen R. Hamilton ◽  
Brenda M. Elliott ◽  
Sarah Shafer Berger ◽  
Neil E. Grunberg

2021 ◽  
pp. 108786
Author(s):  
Sabino Valentina ◽  
Angelo Blasio ◽  
Antonio Ferragud ◽  
Sema G. Quadir ◽  
Malliga R. Iyer ◽  
...  

2017 ◽  
Vol 171 ◽  
pp. e181
Author(s):  
Kaliris Yimar Salas-Ramirez ◽  
Muhammed-Rilwan Muritala ◽  
Soberjot Singh ◽  
Samuel Ayo ◽  
Rina Liang ◽  
...  

1980 ◽  
Vol 186 (1) ◽  
pp. 295-300 ◽  
Author(s):  
S Thrower ◽  
L Lim

The progestin-high-affinity-binding components in rat target tissues have been assayed by a simple and precise procedure by using spheroidal hydroxylapatite. The progestin ‘receptors’ in the uterus and hypothalamus of female rats are highly specific for progestins, which they bind with high affinity (Kd for [3H]progesterone in hypothalamus is 1.9 nM and in uterus is 3.7 nM). The dissociation of [3H]progesterone from receptor in vitro is rapid: t1/2 6 degrees C = 45 min in uterine cytosol; t1/2 6 degrees C = 160 min in hypothalamic cytosol. The binding is destroyed by proteinase. In the cytosol of hypothalamus and cortex of developing rats, progestin ‘receptors’ were present in both male and female rats by 2-3 days after birth; subsequent changes in concentration of these ‘receptors’ appeared to be independent of sex. Concentrations of progestin ‘receptor’ were close to adult values by 8-9 days, and thereafter changed relatively little.


1967 ◽  
Vol 45 (4) ◽  
pp. 451-455 ◽  
Author(s):  
W. S. Schwark ◽  
D. J. Ecobichon

Vertical zone electrophoresis in starch gel was employed in conjunction with various histochemical techniques to characterize the liver and kidney esterases of male and female rats. Tissue-specific patterns were observed for each organ and a sex-dependent difference was noted on electrophoretic separation of the liver extracts. On the basis of substrate specificity and inhibitor sensitivity, both organs were observed to contain similar nonspecific aliesterases or carboxylesterases (EC 3.1.1.1). Inhibition studies showed the presence of two types of aliesterase in the liver and kidney extracts.


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