scholarly journals Prenatal exposure to cocaine alters the development of conditioned place-preference to cocaine in adult mice

2007 ◽  
Vol 87 (4) ◽  
pp. 462-471 ◽  
Author(s):  
C.J. Malanga ◽  
Martina Pejchal ◽  
Barry E. Kosofsky
2017 ◽  
Vol 52 (suppl_1) ◽  
pp. i4-i30
Author(s):  
R Camarini ◽  
A.B. Suárez ◽  
L.B. Hoffmann ◽  
A.V. Rueda ◽  
M.B. Rae ◽  
...  

2007 ◽  
Vol 31 (12) ◽  
pp. 2001-2005 ◽  
Author(s):  
Mei Song ◽  
Xue-Yi Wang ◽  
Mei Zhao ◽  
Xiao-Yi Wang ◽  
Hai-Feng Zhai ◽  
...  

2015 ◽  
Vol 113 ◽  
pp. 81-85 ◽  
Author(s):  
Freddyson J. Martínez-Rivera ◽  
Eduardo J. Natal-Albelo ◽  
Namyr A. Martínez ◽  
Roberto A. Orozco-Vega ◽  
Oscar A. Muñiz-Seda ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Ellen R. Cullity ◽  
Alexandre A. Guerin ◽  
Christina J. Perry ◽  
Jee Hyun Kim

Adolescence marks a particularly vulnerable period to developing substance use disorders. Human and rodent studies suggest that hypersensitivity to reward may contribute towards such vulnerability when adolescents are exposed to casual drug use. Methamphetamine is a popular illicit substance used by male and female youths. However, age- and sex-specific research in methamphetamine is scarce. The present study therefore aimed to examine potential sex differences in methamphetamine-conditioned place preference in adolescent and adult mice. Mice (n = 16–24/group) were conditioned to methamphetamine (0.1 mg/kg). We observed that regardless of age, females were more hyperactive compared to males. Individually normalized score against baseline preference indicated that on average, adolescents formed stronger preference compared to adults in both sexes. This suggests that adolescents are more sensitive to the rewarding effects of methamphetamine compared to adults. Surprisingly, individual data showed that some mice formed a conditioned place aversion instead of preference, with females less likely to form an aversion compared to males. These results suggest that adolescents may be hypersensitive to methamphetamine’s rewarding effects. In addition, female resistance to the aversive effects of methamphetamine may relate to the sex-specific findings in humans, including quicker transition to regular methamphetamine use observed in females compared to males.


2014 ◽  
Vol 25 (5 and 6) ◽  
pp. 532-546 ◽  
Author(s):  
Maria P. García-Pardo ◽  
Marta Rodríguez-Arias ◽  
Concepcion Maldonado ◽  
Carmen Manzanedo ◽  
Jose Miñarro ◽  
...  

2019 ◽  
Vol 181 ◽  
pp. 60-68
Author(s):  
Rosana Camarini ◽  
Lucas Barbosa Hoffmann ◽  
Andrea Suarez ◽  
Mariana Rae ◽  
Tania Marcourakis ◽  
...  

2021 ◽  
Vol 3 ◽  
pp. e24
Author(s):  
Ellen Rose Cullity ◽  
Alexandre Arthur Guérin ◽  
Heather Bronwyn Madsen ◽  
Christina Jennifer Perry ◽  
Jee Hyun Kim

Rodent studies have proposed that adolescent susceptibility to substance use is at least partly due to adolescents experiencing reduced aversive effects of drugs compared to adults. We thus investigated methamphetamine (meth) conditioned place preference/aversion (CPP/CPA) in adolescent and adult mice in both sexes using a high dose of meth (3 mg/kg) or saline as controls. Mice tagged with green-fluorescent protein (GFP) at Drd1a or Drd2 were used so that dopamine receptor 1 (D1) and 2 (D2) expression within the insular cortex (insula) could be quantified. There are sex differences in how the density of D1+ and D2+ cells in the insula changes across adolescence that may be related to drug-seeking behaviors. Immunohistochemistry followed by stereology were used to quantify the density of cells with c-Fos and/or GFP in the insula. Unexpectedly, mice showed huge variability in behaviors including CPA, CPP, or no preference or aversion. Females were less likely to show CPP compared to males, but no age differences in behavior were observed. Conditioning with meth increased the number of D2 + cells co-labelled with c-Fos in adults but not in adolescents. D1:D2 ratio also sex- and age-dependently changed due to meth compared to saline. These findings suggest that reduced aversion to meth is unlikely an explanation for adolescent vulnerability to meth use. Sex- and age-specific expressions of insula D1 and D2 are changed by meth injections, which has implications for subsequent meth use.


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