Extinction of Fear Memory Attenuates Conditioned Cardiovascular Fear Reactivity

被引:12
|
作者
Swiercz, Adam P. [1 ,2 ]
Seligowski, Antonia, V [3 ]
Park, Jeanie [4 ]
Marvar, Paul J. [1 ,2 ,5 ]
机构
[1] George Washington Univ, Dept Pharmacol & Physiol, Washington, DC 20052 USA
[2] George Washington Univ, Inst Neurosci, Washington, DC 20052 USA
[3] Harvard Med Sch, McLean Hosp, Belmont, MA USA
[4] Emory Univ, Sch Med, Atlanta VA Med Ctr, Div Renal Med, Atlanta, GA USA
[5] George Washington Univ, Dept Psychiat & Behav Sci, Washington, DC 20052 USA
来源
关键词
PTSD; fear memory; Pavlovian fear conditioning; cardiovascular disease; extinction; physiological hyperarousal; POSTTRAUMATIC-STRESS-DISORDER; ACOUSTIC STARTLE STIMULUS; CORONARY-HEART-DISEASE; EXTINGUISHED FEAR; BLOOD-PRESSURE; MICE; RESPONSES; INHIBITION; ACTIVATION; DYNAMICS;
D O I
10.3389/fnbeh.2018.00276
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Post-traumatic stress disorder (PTSD) is characterized by a heightened emotional and physiological state and an impaired ability to suppress or extinguish traumatic fear memories. Exaggerated physiological responses may contribute to increased cardiovascular disease (CVD) risk in this population, but whether treatment for PTSD can offset CVD risk remains unknown. To further evaluate physiological correlates of fear learning, we used a novel pre-clinical conditioned cardiovascular testing paradigm and examined the effects of Pavlovian fear conditioning and extinction training on mean arterial pressure (MAP) and heart rate (HR) responses. We hypothesized that a fear conditioned cardiovascular response could be detected in a novel context and attenuated by extinction training. In a novel context, fear conditioned mice exhibited marginal increases in MAP (similar to 3 mmHg) and decreases in HR (similar to 20 bpm) during CS presentation. In a home cage context, the CS elicited significant increases in both HR (100 bpm) and MAP (20 mmHg). Following extinction training, the MAP response was suppressed while CS-dependent HR responses were variable. These pre-clinical data suggest that extinction learning attenuates the acute MAP responses to conditioned stimuli over time, and that MAP and HR responses may extinguish at different rates. These results suggest that in mouse models of fear learning, conditioned cardiovascular responses are modified by extinction training. Understanding these processes in pre-clinical disease models and in humans with PTSD may be important for identifying interventions that facilitate fear extinction and attenuate hyper-physiological responses, potentially leading to improvements in the efficacy of exposure therapy and PTSD-CVD comorbidity outcomes.
引用
收藏
页数:9
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