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New Insights Into the Neural Circuits That Support Pavlovian Fear Conditioning
New Insights Into the Neural Circuits That Support Pavlovian Fear Conditioning
New Insights Into the Neural Circuits That Support Pavlovian Fear Conditioning

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211150956
ISBN  
9798381949650
DDC  
371
저자명  
DiFazio, Lauren Elizabeth.
서명/저자  
New Insights Into the Neural Circuits That Support Pavlovian Fear Conditioning
발행사항  
[Sl] : University of California, Los Angeles, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
102 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-09, Section: B.
주기사항  
Advisor: Adhikari, Avishek.
학위논문주기  
Thesis (Ph.D.)--University of California, Los Angeles, 2024.
초록/해제  
요약Pavlovian fear conditioning is the predominant procedure used to study fear learning in rodents. Decades of research has shown that disrupting activity in the basolateral amygdala (BLA) attenuates the acquisition and storage of fear memories (Cousens & Otto, 1998; Maren, Aharonov & Fanselow, 1996; Phillips & LeDoux, 1992). As a result, current models of fear learning posit that information about the stimuli and aversive event converge and are stored in the BLA (Maren & Quirk, 2004; Pitkanen, Savander & LeDoux, 1997). Per this theory, the BLA should be necessary during both the tone and the shock to form this association. To test this theory, experiment 1 took advantage of the temporal specificity of optogenetics and inhibited the BLA during only the tone or only the shock of Pavlovian fear conditioning. The results show that BLA inhibition during the tone, but not the shock, disrupted fear learning and memory, calling into question the necessity of the BLA for processing the shock. Prior experience has a marked effect on future fear learning, but this research primarily focuses on the detrimental effect of stressful experience. The Sharpe lab recently began exploring how prior positive experiences influence fear learning. They found that the lateral hypothalamus (LH) becomes necessary for fear conditioning after reward learning experience (Sharpe et al., 2021). Experiment 2 investigated whether the BLA remain necessary to support fear learning and memory after LH is implicated in fear learning following reward experience. The BLA was optogenetically inhibited during the cue of fear conditioning in rats with or without reward experience. As expected, BLA inhibition disrupted fear memories in naive rats. However, BLA inhibition did not affect fear memories in rats with reward learning experience. Experiment 3 investigated if brief optogenetic inhibition of the BLA in experiment 2 failed to disrupt the BLA at the crucial time to disrupt fear conditioning because the timescale of the BLA's activity shifted. Using chemogenetics, the BLA was inhibited across acquisition of a tone-shock association in rats with or without reward experience. The results of experiment 3 were inconclusive due to insufficient expression of hm4di. Lastly, experiment 4 inhibited the BLA during fear conditioning in reward experienced rats with or without exposure to chronic unpredictable stress (CUS). Rats that received CUS treatment showed enhanced fear learning, but there was no difference in the effect of BLA inhibition during fear learning. Overall, these experiments demonstrate a new perspective on the canonical theory of fear learning and the BLA and expand on how the newfound role of LH in fear learning affects the importance of the BLA for this process and the importance of considering prior experience in our models of the neural circuits that drive learning and memory. 
일반주제명  
Behavioral psychology
일반주제명  
Neurosciences
일반주제명  
Psychology
키워드  
Basolateral amygdala
키워드  
Fear conditioning
키워드  
Lateral hypothalamus
키워드  
Learning experience
키워드  
Neural circuits
기타저자  
University of California, Los Angeles Psychology 0780
기본자료저록  
Dissertations Abstracts International. 85-09B.
전자적 위치 및 접속  
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MARC

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■040    ▼aMiAaPQ▼cMiAaPQ
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■1001  ▼aDiFazio,  Lauren  Elizabeth.
■24510▼aNew  Insights  Into  the  Neural  Circuits  That  Support  Pavlovian  Fear  Conditioning
■260    ▼a[Sl]▼bUniversity  of  California,  Los  Angeles▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a102  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-09,  Section:  B.
■500    ▼aAdvisor:  Adhikari,  Avishek.
■5021  ▼aThesis  (Ph.D.)--University  of  California,  Los  Angeles,  2024.
■520    ▼aPavlovian  fear  conditioning  is  the  predominant  procedure  used  to  study  fear  learning  in  rodents.  Decades  of  research  has  shown  that  disrupting  activity  in  the  basolateral  amygdala  (BLA)  attenuates  the  acquisition  and  storage  of  fear  memories  (Cousens  &  Otto,  1998;  Maren,  Aharonov  &  Fanselow,  1996;  Phillips  &  LeDoux,  1992).  As  a  result,  current  models  of  fear  learning  posit  that  information  about  the  stimuli  and  aversive  event  converge  and  are  stored  in  the  BLA  (Maren  &  Quirk,  2004;  Pitkanen,  Savander  &  LeDoux,  1997).  Per  this  theory,  the  BLA  should  be  necessary  during  both  the  tone  and  the  shock  to  form  this  association.  To  test  this  theory,  experiment  1  took  advantage  of  the  temporal  specificity  of  optogenetics  and  inhibited  the  BLA  during  only  the  tone  or  only  the  shock  of  Pavlovian  fear  conditioning.  The  results  show  that  BLA inhibition  during  the  tone,  but  not  the  shock,  disrupted  fear  learning  and  memory,  calling  into  question  the  necessity  of  the  BLA  for  processing  the  shock.  Prior  experience  has  a  marked  effect  on  future  fear  learning,  but  this  research  primarily  focuses  on  the  detrimental  effect  of  stressful  experience.  The  Sharpe  lab  recently  began  exploring  how  prior  positive  experiences  influence  fear  learning.  They  found  that  the  lateral  hypothalamus  (LH)  becomes  necessary  for  fear  conditioning  after  reward  learning  experience  (Sharpe  et  al.,  2021).  Experiment  2  investigated  whether  the  BLA  remain  necessary  to  support  fear  learning  and  memory  after  LH  is  implicated  in  fear  learning  following  reward  experience.  The  BLA  was  optogenetically  inhibited  during  the  cue  of  fear  conditioning  in  rats  with  or  without  reward  experience.  As  expected,  BLA  inhibition  disrupted  fear  memories  in  naive  rats.  However,  BLA  inhibition  did  not  affect  fear  memories  in  rats  with  reward  learning  experience.  Experiment  3  investigated  if  brief  optogenetic  inhibition  of  the  BLA  in  experiment  2  failed  to  disrupt  the  BLA  at  the  crucial  time  to  disrupt  fear  conditioning  because  the  timescale  of  the  BLA's  activity  shifted.  Using  chemogenetics,  the  BLA  was  inhibited  across  acquisition  of  a  tone-shock  association  in  rats  with  or  without  reward  experience.  The  results  of  experiment  3  were  inconclusive  due  to  insufficient  expression  of  hm4di.  Lastly,  experiment  4  inhibited  the  BLA  during  fear  conditioning  in  reward  experienced  rats  with  or  without  exposure  to  chronic  unpredictable  stress  (CUS).  Rats  that  received  CUS  treatment  showed  enhanced  fear  learning,  but  there  was  no  difference  in  the  effect  of  BLA  inhibition  during  fear  learning.  Overall,  these  experiments  demonstrate  a  new  perspective  on  the  canonical  theory  of  fear  learning  and  the  BLA  and  expand  on  how  the  newfound  role  of  LH  in  fear  learning  affects  the  importance  of  the  BLA  for  this  process  and  the  importance  of  considering  prior  experience  in  our  models  of  the  neural  circuits  that  drive  learning  and  memory. 
■590    ▼aSchool  code:  0031.
■650  4▼aBehavioral  psychology
■650  4▼aNeurosciences
■650  4▼aPsychology
■653    ▼aBasolateral  amygdala
■653    ▼aFear  conditioning
■653    ▼aLateral  hypothalamus
■653    ▼aLearning  experience
■653    ▼aNeural  circuits
■690    ▼a0384
■690    ▼a0317
■690    ▼a0621
■71020▼aUniversity  of  California,  Los  Angeles▼bPsychology  0780.
■7730  ▼tDissertations  Abstracts  International▼g85-09B.
■790    ▼a0031
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17160321▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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