scholarly journals Adolescent Rats Find Repeated Δ9-THC Less Aversive Than Adult Rats but Display Greater Residual Cognitive Deficits and Changes in Hippocampal Protein Expression Following Exposure

2007 ◽  
Vol 33 (5) ◽  
pp. 1113-1126 ◽  
Author(s):  
Heidi R Quinn ◽  
Izuru Matsumoto ◽  
Paul D Callaghan ◽  
Leonora E Long ◽  
Jonathon C Arnold ◽  
...  
2017 ◽  
Vol 55 (1) ◽  
pp. 26-41 ◽  
Author(s):  
Ane Murueta-Goyena ◽  
Naiara Ortuzar ◽  
Pascual Ángel Gargiulo ◽  
José Vicente Lafuente ◽  
Harkaitz Bengoetxea

1978 ◽  
Vol 43 (1) ◽  
pp. 209-210
Author(s):  
Nicholas C. Kierniesky

Previous research found significantly more free exploration in immature and adult albino rats compared to adolescent rats. The present study indicated this to be true only in adult rats (N = 12). Housing procedures prior to testing may explain the lack of replication.


2012 ◽  
Vol 302 (12) ◽  
pp. F1640-F1649 ◽  
Author(s):  
Maki Nomura ◽  
Hideyuki Motohashi ◽  
Hiroko Sekine ◽  
Toshiya Katsura ◽  
Ken-ichi Inui

Organic anion transporters (OAT1 and OAT3) and multidrug resistance-associated proteins (MRP2 and MRP4) play important roles in anionic drug secretion in renal proximal tubules. Changes in the expression of such transporters are considered to affect the tubular secretion of anionic drugs. The purpose of this study was to elucidate the developmental changes in the expression of OAT1, OAT3, MRP2, and MRP4 and their effects on the tubular secretion of drugs. The mRNA level of each transporter was measured by real-time PCR, and the protein expression was evaluated by Western blotting and immunohistochemical analysis. In addition, the tubular secretion of phenolsulfonphthalein (PSP) in infant (postnatal day 14) and adult rats was estimated based on in vivo clearance study. The protein expression of organic anion transporters were very low at postnatal day 0 and gradually increased with age. In postnatal day 14 rats, the expression of OAT1 and OAT3 seemed to be at almost mature levels, while MRP2 and MRP4 seemed to be at immature levels. Immunohistochemical analysis in the kidney of postnatal day 0 rats revealed OATs on the basolateral membrane and MRPs on the brush-border membrane. At postnatal day 0, the distribution of these transporters was restricted to the inner cortical region, while after postnatal day 14, it was identical to that in adult kidney. An in vivo clearance study revealed that the tubular secretion of PSP was significantly lower in postnatal day 14 rats than adult rats. These results indicate that age-dependent changes in organic anion transporter expression affect the tubular secretion of anionic drugs in pediatric patients.


2014 ◽  
Vol 182 (1) ◽  
pp. 60 ◽  
Author(s):  
M. E. Forbes ◽  
M. Paitsel ◽  
J. D. Bourland ◽  
D. R. Riddle

1985 ◽  
Vol 63 (9) ◽  
pp. 1113-1121 ◽  
Author(s):  
Norman S. Track ◽  
Margaret E. Cawkwell ◽  
Beth C. Chin ◽  
Susan S. Chiu ◽  
Sean A. Haberer ◽  
...  

Metabolic responses to short- and long-term guar gum consumption were studied in adolescent and adult rats. For the Song-term study, male adolescent rats were divided into four groups (n = 60/group) and fed guar gum, cellulose, or bran diet for 67 weeks. Metabolic studies (food–water intake, feces–urine output, body weight, carbohydrate tolerance) were performed eight times during the 67 weeks. The guar gum group consumed less diet throughout the entire study and gained less weight over the first 20 weeks compared with the cellulose and bran groups. A second bran-fed group was food restricted over the first 20 weeks to match the reduced weight gain of the guar gum group and then fed ad libitum. Reduced plasma glucose excursions were measured for only the guar gum group after both fibre-free glucose and sucrose challenges at weeks 6, 12, and 18; from 24 to 64 weeks all four groups had similar glucose tolerance responses. Twenty-four hour urinary glucose excretion was similar during all eight metabolic studies up to 64 weeks for guar gum and cellulose groups. In the short-term study, male adolescent (200 g; n = 10/group) and adult (630 g; n = 15/group) rats were divided into five and four groups, respectively, and fed guar gum, guar by-product (GBP), cellulose, or bran diet for 6 weeks. A metabolic study was performed during the 6th week. Adolescent rats fed guar gum or GBP diets gained less weight than the cellulose group; only the guar gum group displayed improved carbohydrate tolerance. Adult rats had similar weight gain and carbohydrate tolerance responses to the four diets. Both adolescent and adult rats fed GBP had significantly reduced 24-h urinary glucose excretion. These studies suggest that adolescent rats respond to guar gum consumption with reduced body weight gain and improved carbohydrate tolerance and demonstrate that these responses are lost or absent in adult rats.


2000 ◽  
Vol 23 (1) ◽  
pp. 11-19 ◽  
Author(s):  
John D. Frank ◽  
Troy W. McKelvey ◽  
Andrew R. Kraynak ◽  
Phillip R. Hertzog ◽  
Richard D. Storer

2021 ◽  
Author(s):  
Jocelyn Breton ◽  
Jordan S. Eisner ◽  
Vaidehi S. Gandhi ◽  
Natalie Musick ◽  
Aileen Zhang ◽  
...  

Prosocial behavior, in particular helping others in need, occurs preferentially in response to the perceived distress of one's own group members, or ingroup. The development of neural mechanisms underlying social selectivity towards ingroup members are not well established. Here, we used a rat helping behavior test to explore the development and neural basis of ingroup bias for prosocial behavior in adolescent rats. We previously found that adult rats selectively help others from their own social group, and that this selectivity is associated with activation in reward and motivation circuits. Surprisingly, we found that adolescent rats helped both ingroup and outgroup members, evidence suggesting that ingroup bias emerges in adulthood. Analysis of brain-wide neural activity, indexed by expression of the early-immediate gene c-Fos, revealed increased activity for ingroup members across a broad set of regions, which was congruent for adults and adolescents. However, adolescents showed reduced hippocampal and insular activity, and increased orbitofrontal cortex activity compared to adults. Adolescent rats who did not help trapped others also demonstrated increased amygdala connectivity. Together, these findings demonstrate that biases for group-dependent prosocial behavior develop with age in rats and suggest that specific brain regions contribute to this prosocial selectivity, overall pointing to possible targets for the functional modulation of ingroup bias.


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