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TPH2 knockout rats cannot accept social defeat in resident-intruder test. / Zhukov, Ilya; Nemets, Vsevolod; Alnefeesi, Yazen; Shabanov, Petr; Alenina, Natalia; Gainetdinov, Raul.

FENS 24 . 2024. (Science Communications World Wide).

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@inbook{da3d1fc659d44a65acf8f9befea1c071,
title = "TPH2 knockout rats cannot accept social defeat in resident-intruder test",
abstract = "Brain serotonin (5-HT) is one of the key regulators of aggressive behavior and social defeat stress mechanisms. We had previously found that abolishing central 5-HT biosynthesis increases aggression, as tryptophan hydroxylase 2 (Tph2-/-) knockout rats (TPH2-KO) are more aggressive than wild-type (WT) counterparts. In this elaboration, we compared different types of intruders to expand our understanding of the aggressive phenotype in TPH2-KO rats. The resident-intruder paradigm was applied to evaluate the territorial aggression of rats, where isolated residents (TPH2-KO, WT male, 36 weeks, n=9), were presented with socialized intruders, either 50% smaller (S-I) or 30% larger by weight (L-I). The behavioral profile of TPH-2-KO rats was similar to WT with respect to the S-I group, but showed significantly more aggression when presented with the larger animals of the L-I group. Compared to WT, the TPH-2-KO initiated their attacks sooner (p = 0. 0001), fought for longer periods (p = 0. 0002), and spent less time in non-social exploration (p = 0.0014). Residents from both the WT and TPH-2-KO groups tended to cease their attacks upon the submission of smaller animals. However, while WT residents behave similarly with the L-I intruders, the TPH-2-KO spent much more time attacking the larger animals. These results demonstrate that highly aggressive behavior in TPH2-KO rats can be associated not with a depressive-like state caused by lack of 5-HT, but with a strong motivation towards advancing in the social dominance hierarchy. This work was supported by the project ID:95444211 of the St.Petersburg State University, St.Petersburg, Russia.",
author = "Ilya Zhukov and Vsevolod Nemets and Yazen Alnefeesi and Petr Shabanov and Natalia Alenina and Raul Gainetdinov",
year = "2024",
month = jun,
doi = "10.57736/ade6-3334",
language = "English",
series = "Science Communications World Wide",
booktitle = "FENS 24",
note = "FENS Forum 2024 , FENS 24 ; Conference date: 25-06-2024 Through 29-06-2024",

}

RIS

TY - CHAP

T1 - TPH2 knockout rats cannot accept social defeat in resident-intruder test

AU - Zhukov, Ilya

AU - Nemets, Vsevolod

AU - Alnefeesi, Yazen

AU - Shabanov, Petr

AU - Alenina, Natalia

AU - Gainetdinov, Raul

PY - 2024/6

Y1 - 2024/6

N2 - Brain serotonin (5-HT) is one of the key regulators of aggressive behavior and social defeat stress mechanisms. We had previously found that abolishing central 5-HT biosynthesis increases aggression, as tryptophan hydroxylase 2 (Tph2-/-) knockout rats (TPH2-KO) are more aggressive than wild-type (WT) counterparts. In this elaboration, we compared different types of intruders to expand our understanding of the aggressive phenotype in TPH2-KO rats. The resident-intruder paradigm was applied to evaluate the territorial aggression of rats, where isolated residents (TPH2-KO, WT male, 36 weeks, n=9), were presented with socialized intruders, either 50% smaller (S-I) or 30% larger by weight (L-I). The behavioral profile of TPH-2-KO rats was similar to WT with respect to the S-I group, but showed significantly more aggression when presented with the larger animals of the L-I group. Compared to WT, the TPH-2-KO initiated their attacks sooner (p = 0. 0001), fought for longer periods (p = 0. 0002), and spent less time in non-social exploration (p = 0.0014). Residents from both the WT and TPH-2-KO groups tended to cease their attacks upon the submission of smaller animals. However, while WT residents behave similarly with the L-I intruders, the TPH-2-KO spent much more time attacking the larger animals. These results demonstrate that highly aggressive behavior in TPH2-KO rats can be associated not with a depressive-like state caused by lack of 5-HT, but with a strong motivation towards advancing in the social dominance hierarchy. This work was supported by the project ID:95444211 of the St.Petersburg State University, St.Petersburg, Russia.

AB - Brain serotonin (5-HT) is one of the key regulators of aggressive behavior and social defeat stress mechanisms. We had previously found that abolishing central 5-HT biosynthesis increases aggression, as tryptophan hydroxylase 2 (Tph2-/-) knockout rats (TPH2-KO) are more aggressive than wild-type (WT) counterparts. In this elaboration, we compared different types of intruders to expand our understanding of the aggressive phenotype in TPH2-KO rats. The resident-intruder paradigm was applied to evaluate the territorial aggression of rats, where isolated residents (TPH2-KO, WT male, 36 weeks, n=9), were presented with socialized intruders, either 50% smaller (S-I) or 30% larger by weight (L-I). The behavioral profile of TPH-2-KO rats was similar to WT with respect to the S-I group, but showed significantly more aggression when presented with the larger animals of the L-I group. Compared to WT, the TPH-2-KO initiated their attacks sooner (p = 0. 0001), fought for longer periods (p = 0. 0002), and spent less time in non-social exploration (p = 0.0014). Residents from both the WT and TPH-2-KO groups tended to cease their attacks upon the submission of smaller animals. However, while WT residents behave similarly with the L-I intruders, the TPH-2-KO spent much more time attacking the larger animals. These results demonstrate that highly aggressive behavior in TPH2-KO rats can be associated not with a depressive-like state caused by lack of 5-HT, but with a strong motivation towards advancing in the social dominance hierarchy. This work was supported by the project ID:95444211 of the St.Petersburg State University, St.Petersburg, Russia.

U2 - 10.57736/ade6-3334

DO - 10.57736/ade6-3334

M3 - Conference abstracts

T3 - Science Communications World Wide

BT - FENS 24

T2 - FENS Forum 2024

Y2 - 25 June 2024 through 29 June 2024

ER -

ID: 121644983