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1 e resident-intruder model for social stress (social defeat).
2 d immobility in the forced swim test, as did social defeat.
3 ojections mimicked the behavioral effects of social defeat.
4 th addiction and depression models including social defeat.
5 d decreased neurogenesis are consequences of social defeat.
6 conomic status) and mice subject to repeated social defeat.
7 red for restoration of normal behavior after social defeat.
8 ls, none of these molecules were affected by social defeat.
9 precipitating the depressive phenotype after social defeat.
10 that were susceptible, but not resilient to social defeat.
11 scimol on aggression were dependent on prior social defeat.
12 ith a novel intruder 24 hours after an acute social defeat.
13 or not a hamster has previously experienced social defeat.
14 gs of miniature EPSCs (mEPSCs) in mice after social defeat.
15 an increase in the frequency of mEPSCs after social defeat.
16 TLR4) and macrophages (CD14 and CD86) after social defeat.
17 e to reverse behavioral pathology induced by social defeat.
18 al warm temperature also was evaluated after social defeat.
19 nhances the activation of orexin cells after social defeat.
20 t make some mice resistant to the effects of social defeat.
21 changes in cholecystokinin (CCK-8) following social defeat.
22 NST to modulate agonistic behavior following social defeat.
23 n male and female California mice exposed to social defeat.
24 no effect was observed on other symptoms of social defeat.
25 d signaling molecules in response to chronic social defeat, 2) brain reward function during social de
26 o subthreshold stress (i.e., single cycle of social defeat) 24 days after RSD, and immune and behavio
27 DRN GABA and 5-HT neurons in mice exposed to social defeat, a model that induces long-lasting avoidan
28 ses in IkappaB kinase (IKK) in the NAc after social defeat, a molecular pathway that has been shown t
31 about how a behavioral interaction, such as social defeat, alters the development of adaptive immuni
33 on during the circadian peak, adrenalectomy, social defeat and acute injections of alcohol on these c
34 social avoidance in mice exposed to chronic social defeat and concurrently prevented the electrophys
37 cial defeat, 2) brain reward function during social defeat and long-term treatment with the antidepre
39 in neurogenesis drive changes in mood after social defeat and that glucocorticoids secreted during e
40 te) granulocytes in mice subject to repeated social defeat, and these effects were blocked by pharmac
42 ults highlight more robust CCK modulation by social defeat as compared with 3 other neuropeptide syst
44 ce that are repeatedly subjected to bouts of social defeat by a larger and aggressive CD-1 mouse resu
45 at an inbred population of mice subjected to social defeat can be separated into susceptible and unsu
48 ffected with MDD and rats exposed to chronic social defeat (CSD) stress, which is used to model depre
49 missive behavior and exhibited resilience to social defeat, demonstrated by a lack of subsequent soci
50 cial disruption (SDR) that involves repeated social defeat during intermale aggression results in inc
52 mygdala (BLA) of animals that are exposed to social defeat enhances subsequent defeat-induced changes
53 ol group, and active coping behaviors during social defeat episodes were associated with subsequent r
56 Sprague-Dawley rats were exposed to repeated social defeat for 5 days while controls were placed in a
61 ere we investigated behavioral adaptation to social defeat in mice and uncovered a critical contribut
63 ents compared behavioral effects of repeated social defeat in mice with forebrain GR deletion and in
69 nalysis of microglia indicated that repeated social defeat increased levels of interleukin (IL)-1beta
73 (mPFC) neuronal activity is associated with social defeat-induced depression- and anxiety-like behav
75 bition of Rac1 activity in the NAc increases social defeat-induced social avoidance and anhedonia in
76 e gyrus of the hippocampus of LR rats led to social defeat-induced social avoidance, whereas its acti
80 activation of IKK signaling pathways during social defeat is both necessary and sufficient to induce
85 ute to spatial memory deficits in the rodent social defeat model that can be reversed by anti-inflamm
88 e examined acute and long-lasting effects of social defeat on OT neurons in male and female Californi
89 with or without subsequent exposure to adult social defeat on slc6a4 mRNA expression in the dorsal ra
90 ogically relevant stressor, namely threat of social defeat, on dopamine concentrations in nucleus acc
93 tine's antidepressant effects in the chronic social defeat paradigm, whereas inhibition of CaMKII act
97 ne neurons of mice undergoing a subthreshold social-defeat paradigm rapidly induced a susceptible phe
98 expression, reveals clear differences in the social defeat phenotype induced by Fosb gene manipulatio
99 the pVTA and CRF-R2 in the aVTA during each social defeat prevented escalated cocaine self-administr
100 demonstrates that the experience of repeated social defeat prior to a primary viral infection signifi
102 In Syrian hamsters (Mesocricetus auratus), social defeat produces a subsequent increase in submissi
116 ehavioral analysis confirmed that the 14-day social defeat sessions resulted in induction of depressi
119 e socially avoidant by the stress of chronic social defeats showed depressed neural activity in the l
120 inistration of cocaine immediately following social defeat significantly reduced the number of Fos-LI
121 rate that adult mice which underwent chronic social defeat stress (CSDS) displayed elevated anxiety-l
124 nt-like activity of vmPFC DBS in the chronic social defeat stress (CSDS) model of depression (n = 8-1
126 monitored in mice after exposure to chronic social defeat stress (CSDS), a model of prolonged psycho
127 educed in NAc of mice susceptible to chronic social defeat stress (CSDS), a paradigm that produces be
128 Here we examined the effects of chronic social defeat stress (CSDS), an ethological form of stre
132 was microinjected into the VTA 20 min before social defeat stress (or handling) on days 1, 4, 7, and
134 ter exposure to either subthreshold repeated social defeat stress (RSDS) or a purely emotional stress
135 Numerous studies have employed repeated social defeat stress (RSDS) to study the neurobiological
139 iciency leads to increased susceptibility to social defeat stress (SDS), a model of psychosocial stre
140 ed enhanced susceptibility to a subthreshold social defeat stress (SSDS) as observed by reduced socia
143 a2 subunit knockdown decreased resilience to social defeat stress and c-fos immunoreactivity in the B
144 tal period increases susceptibility to adult social defeat stress and causes long-lasting transcripti
145 oth the decrease in Rac1 transcription after social defeat stress and depression-related behavior, su
146 r, we find that female mice undergo repeated social defeat stress and develop social avoidance, decre
148 VL function renders mice more susceptible to social defeat stress and promotes depression-like behavi
149 e-induced behaviors, indicating that chronic social defeat stress and repeated cocaine exposure regul
150 e exposed mice to chronic cocaine or chronic social defeat stress and used two-photon laser scanning
157 tudy, the authors investigated the impact of social defeat stress during mid-adolescence on adult mal
161 tidepressant action, we administered chronic social defeat stress followed by chronic imipramine (a t
162 D2-MSNs after CSDS or before a subthreshold social defeat stress in D1-Cre or D2-Cre bacterial artif
163 resent study, we investigated the effects of social defeat stress in male rats on the operant escape
172 h wild-type mice; and 5) exposure to chronic social defeat stress induces blood glucocorticoids and a
176 rainstem structures after a brief episode of social defeat stress is related to behavioral sensitizat
177 this study we show that a single episode of social defeat stress is sufficient to specifically induc
182 1, 14, 17, and 20, animals were subjected to social defeat stress or a nonstressful control condition
183 at DeltaFosB is induced in NAc after chronic social defeat stress or after chronic antidepressant tre
184 a separate group of rats underwent a single social defeat stress or control handling and were challe
185 ue-Dawley rats underwent a single episode of social defeat stress or control handling, followed by am
186 Lymphocytes from mice undergoing chronic social defeat stress or from unstressed control mice wer
187 d cocaine administration prior to subchronic social defeat stress potentiated depressive-like behavio
188 and in the tail suspension test and chronic social defeat stress procedure in C57BL/6 male mice.
191 enhanced alcohol consumption in response to social defeat stress relative to their wild-type litterm
193 active Rac1 in the NAc of mice after chronic social defeat stress reverses depression-related behavio
194 entate gyrus neurogenesis is increased after social defeat stress selectively in mice that display pe
195 velop depressive-like symptoms after chronic social defeat stress show distinct changes in the activi
197 rd-associated region, in response to chronic social defeat stress was both necessary and sufficient f
202 sant, ketamine, in mice subjected to chronic social defeat stress, a validated depression model, and
205 induced relapse to cocaine use in rats using social defeat stress, an ethologically valid psychosocia
206 In the present study, we show that chronic social defeat stress, an ethologically validated model o
208 and synaptic results were obtained following social defeat stress, and intracerebroventricular inject
210 electively in susceptible mice after chronic social defeat stress, and overexpression of DeltaFosB in
211 vivo, ACY-738 promoted resilience to chronic social defeat stress, and serotonin-selective viral over
214 downregulated in NAc of mice susceptible to social defeat stress, effects not seen in resilient mice
215 (P70), reactivity to aversive stimuli (i.e., social defeat stress, forced swimming, and elevated plus
217 rimental approaches for studying depression, social defeat stress, in particular, has been shown to h
218 the induction of depressive-like symptoms by social defeat stress, low-novelty-seeking rats [low resp
220 yed increased susceptibility to subthreshold social defeat stress, suggesting that neuronal VGF, expr
221 ctrophysiological adaptations in response to social defeat stress, which are normalized by antidepres
222 course of cross-sensitization after a single social defeat stress, which normally produces transient
223 males as one commonly used paradigm-chronic social defeat stress-has proven challenging to implement
224 K signaling results in a reversal of chronic social defeat stress-induced social avoidance behavior.
253 in levels in plasma are reduced in a chronic social-defeat stress model of depression, which correlat
254 e reward signals, is upregulated by repeated social-defeat stress, a highly validated mouse model of
258 n this model, hamsters that have experienced social defeat subsequently display only submissive-defen
259 class III histone deacetylase, after chronic social defeat suggest a role for this enzyme in mediatin
260 as MDL 11,939 blocks 5-HT2A receptors during social defeat to disrupt the development of the conditio
261 , or 2.0 mg/kg) was injected either prior to social defeat training or prior to conditioned defeat te
262 , or 3.0 mg/kg) was injected either prior to social defeat training or prior to conditioned defeat te
263 h SHI reported experiencing more feelings of social defeat (U=109, z=-2.09, P=.04) and loneliness (U=
265 on in all regions studied in mice 24 h after social defeat when compared to control (naive) mice (P<0
266 antagonist directly into the VTA before each social defeat would prevent the development of later (1)
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