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. 2010 Jan 8;3:68. doi: 10.3389/neuro.09.068.2009

Table 1.

Summary of findings on hippocampus and amygdala.

Article N Human/Animal Sex Age of adversity Test during or post adversity Age at test Adversity Findings
Admon et al. (2009) 50 Human adults 25M/25F 18 years Within 6 months post stress 19 years Combat exposure 1. Amygdala Reactivity pre stress predicted increase in stress-related symptomology.
2. Increases in Hippocampal reactivity predicted increases in stress-related symptomology
Gilbertson et al. (2002) 35 Human adult 12M Combat exposed Twin pairs/23 M noncombat exposed twin pairs Adulthood Post 52.8/51.8 Combat exposure 1. Small hippocampal volume is a risk factor for PTSD. No effect of combat stress on volume
Kasai et al. (2008) 41 Human adult 18M Combat exposed Twin pairs/23 M noncombat exposed twin pairs Adulthood Post 52.8/51.8 Combat exposure 1. Combat exposed twin with PTSD showed decreased hippocampal activity relative to combat exposed twin without PTSD
Liberzon et al. (1999) 39 Human adult 14M Combat Exposure and PTSD/11M Combat only/ 14M Control Adulthood Post 45–52 Combat exposure/current anxiety disorder 1. PTSD patients exhibited elevated activation of left amygdala to combat sounds for
Rauch et al. (2000) 16 Human adult 8M Combat Veterans with PTSD/8 Controls Adulthood Post 48–61 years Combat exposure/current anxiety disorder 1. Combat Exposed Veterans with PTSD had exaggerated amygdala responses to faces
Shin et al. (2004) 36 Human adult 17 (7M) Combat Exposed Veterans with PTSD/19(9M) Combat Exposed Veterans without PTSD Adulthood Post adulthood Combat exposure/current anxiety disorder 1. Male Combat Veterans with PTSD exhibited elevated amygdala activity
Shin et al. (2004) 16 Human adult 8M Firefighters with PTSD/8M Controls Adulthood Post adulthood Fire fighting exposure/current anxiety disorder 1. Participants with PTSD showed decreased hippocampal activation during memory task.
2. Participants with PTSD had smaller hippocampal volume than controls
Gianaros et al. (2007) 48 Human adults 48 F Adulthood During 48 years Self report of stress on perceived stress scale for 20 years 1. Decreases hippocampal volume associated with increased life stress
Armony et al. (2005) 13 Human adults 9F/4M Adulthood Post (within past 4–6 weeks) 19–57 years Motor vehicle accidents 1. Increased amygdala activation to masked fearful faces > masked happy faces
Andersen et al. (2008) 43 Human adults 26F with abuse; 17F healthy controls Childhood Post 18–22 years Retrospective sexual abuse reporting 1. Sexual abuse at 3–5 or 11–13 years of age was associated with reductions in hippocampal volume. 2. Sexual abuse at 9–10 and 14–16 years was not
Bremner et al. (1997) 34 Human adult 12M/5F with child abuse; 12M/5F matched controls Childhood Post 30–50 years Chronic child abuse (at least once a month for a year) 1. PTSD patients have smaller hippocampus and unchanged amygdala
Cohen et al. (2006) 250 Human adult Sex unreported; 100 with 2 or more early negative events/150 with less than 2 negative events Childhood Post 18–70 years; mean age 40 years Retrospective reporting of early life stressors (various) 1. Differences in hippocampal volume were marginally significant and amygdala were nonsignificant between groups
Driessen et al. (2000) 42 Human adults 21F patients with borderline personality disorder/21 age, gender, handedness matched contents Childhood Post 21–40 years Childhood trauma/current borderline personality disorder 1. Patients had 16% smaller hippocampal volume and 8% smaller amygdala than controls
Schmahl et al. (2003) 33 Human adult 10F with Borderline Personality Disorder and childhood trauma/10F controls with childhood trauma/13F controls with no trauma Childhood Post 20–39 years Childhood trauma/Borderline Personality Disorder (BPD) 1. Patients with BPD had smaller amygdala (∼22%) and hippocampal (∼14%) volumes; Trauma exposure only was not tested
Carrion et al. (2001) 24 Human children 14M/10F with trauma and PTSD or subthreshold PTSD; 14M/10 Fage matched controls Childhood Post 7–14 years Various traumatic exposures No differences in hippocampal volume
DeBellis et al. (1999a) 52 Human children 44 Children with PTSD (25M)/61 Control (36M) Childhood Post 8–13 years Childhood maltreatment/current anxiety disorder 1. Decreased intercranial and cerebral volume, increased ventricle size.
2. No differences in hippocampal volume
DeBellis et al. (2001) 18 Human children 9 Children with PTSD(5M)/9 age, gender, Tanner Stage matched Controls Childhood/ pre-puberty Post Pre (10 years)/post (13 years) puberty; longitudinal design Childhood maitreatment/current anxiety disorder 1. No significant decrease in hippocampal volume for children with PTSD across adolescence in a longitudinal design
Tottenham et al. (2009b) 62 Human children 8M/26F previously institutionalized; 5M/23F comparison Infancy Post 5–12 years Adverse caregiving 1. Larger amygdala volume in previously institutionalized group.
2. No differences in hippocampal volume
Mehta et al. (2009) 25 Human children 6M/8F previously institutionalized; 6M/5F comparison Infancy Post 16 years Adverse caregiving 1. Larger amygdala volume in previously institutionalized group.
2. No differences in hippocampal volume
Conrad et al. (1999) 72 Sprague-Dawley rat 36M chronically stressed/ 36M no stress Adulthood 0, 10, and 20-days post stress termination Adulthood 6 h of restraint stress for 21 consecutive days 1. Decreased hippocampal CA3 apical dendrite morphology.
2. 10 or 20 days of recovery eliminated changes in dendritic morphology caused by stress
Honkaniemi et al. (1992) 24 Sprague-Dawley rat 20 Capsaicin/4 Control Adulthood Post Adulthood Capsaicin 1. Expression of c-fos, c-jun, and junB in the PVN and central nucleus of the amygdala
Kim et al. (2001) 28 Long-Evans rats 28M Adulthood Post Adulthood Restraint/tail shock 1. Lesioning the amygdala pre-stress protected hippocampal structure (LTP) and function (Morris Water Maze) effects of stress exposure
Vyas et al. (2002) 3 groups Adult Wistar rats Male Wistar Rats (Chronic Immobilization Stress/Chronic Variable Stress/Control 2-months old (adulthood) Directly after stress 3-months old (adulthood) Chronic immobilization stress/chronic variable stress 1. Accelerated dendritic arborization in the amygdala.
2. Dendritic atrophy in CA3 (hippocampus)
Vyas et al. (2004) 3 groups Adult Wistar rats Male Wistar Rats (Chronic Immobilization Stress/Chronic Variable Stress/ Control 2.5–3 months old (adulthood) Post 3.5–4 months old (adulthood) Chronic immobilization stress 1. Anxiety behavior and amygdala dendtric arborization persisted in stressed rats compared to control.
2. Hippocampal dendritic atrophy did not persist after 21 days of recovery
Liu et al. (1997) Norway rat Several large liters PND 1–10 Post Adulthood Reduced maternal care 1. Increased adrenocorticotropin and corticosterone to stress, decreased hippocampal GR mRNA
Plotsky et al. (2005) 20 Long evans hooded rats 5M non-handled/ 5M handled/5M maternal separation/5 M control PND2–14 Post PND 100–120 Maternal separation 1. Elevated CRH mRNA in Amygdala of Maternally separated and non-handled rats
Brunson et al. (2005) Sprague-Dawley rat Several male litters PND2-weaning Post 4-and 12-months old Poor maternal care 1. Impaired hippocampal function appeared only in middle aged adults
Tsoory et al. (2008) 104 Sprague-Dawley rat 56M exposed to juvenile stress/48M control PND 27–29 Post PND 33 - juvenile/9-week-old adult 3-day variable stress exposure 1. Increased neural cell adhesion molecule in basolateral amygdala, hippocampus CA1, dentate gyrus, entorhinal cortex measured at adulthood but not during the juvenile period
Andersen and Teicher (2004) 100 Sprague-Dawley rat 50M/50F PND 2–20 Post PND 25, 40, 60, 80, 100 Maternal separation 1. Synaptophysin OD decreases in hippocampal CA1 and CA3 at postnatal day 60 (not before).
2. No effect on Synaptophysin OD in the amygdala
Ono et al. (2008) 148 Balb/c mice 76 (33M) early weaned/ 72 (34M) typically weaned PND 14 Post 3, 5, and 8 weeks of age Early weaning (PND 14) 1. Precocious development of amygdala, not hippocampus (accumulation of galactosylceramide) at 5 weeks of age
Chen et al. (2006) 55 Sprague-Dawley rat 55 stressed PND 18 and Adult (3 months old) Directly after stress PND 18 and Adult Restraint/restraint-noise 1. Hippocampal response (FOS) to stress was more rapid and robust at PND 18 than adulthood
Kikusui and Mori (2009) 129 Balb/c mice 63(28M) early weaned/66 (32M) typically weaned PND 14 Post 8–22 weeks Early weaning (PND 14) 1. Accelerated amygdala development
Salzberg et al. (2007) 29 Wistar rats 16 (9M) maternal separation/13 (6 M) early handling PND 2–14 Post 7 weeks Maternal Separation 1. Amygdala sensitization following maternal separation
Isgor et al. (2004) 156 Juvenile Sprague Dawley rats 156M PND 28 24 h post stress/ 3 weeks post stress PND 57/77 28 days of variable chronic stress 1. 3 weeks post stress when rodents were adults hippocampal volume (CA1 and CA3) was decreased due to inhibited growth.
2. 24-h post stress when rodents were still juvenile hippocampal volume differences were absent or reversed
Becker et al. (2007) 20 Octodon Degus 10M stressed/10M non-stressed PND 1–21 Post stress PND 22 (post weaning/pre reproduction) PND1–21 separated 1x per day for 1 h 1. Higher levels of CRF neurons in basolateral amygdala.
2. Lower levels of corticotropin releasing factor (CRF) fibers/neurons in central amygdala and hippocampal dentate gyrus and CA1
Vazquez et al. (2006) 300 Hybrid Sprague-Dawley/Long-Kvans 80 (40M) stress at PND 6/ 80(40M) stress at PND 12/80(40M) stress at PND 18/ 60(30M) controls PND 6, 12, or 18 Directly after, 1 h after, or 4 h after PND 6, 12, or 18 Maternal separation and restraint stress 1. Basal CRH gene expression is higher at earlier ages in amygdala than hippocampus.
2. Deprivation had site-specific effects on the temporal response to restraint stress
Vazquez et al. (1996) 12 groups Juvenile Wistar rats Stressed at PND 6, 9, or 18/ challenged at PND 6, 9, 18/ control PND 6, 9,18 PND 6/9/18 1-h post stress PND 6/9/18 Maternal deprivation/saline injection 1. Mineral corticoid receptor (MR) and glucocorticoid receptor (GR) mRNA decreases in hippocampus of deprived pups
Moriceau et al. (2004) 108 Juvenile Long Evans rats Approximately 1/2 M PND 8 or 12 During stress PND 8 or 12 Predator odor 1. Exogenously administered Cortisol increased amygdala activation and fear responding in young rats
Hatalski et al. (1998) 2 litters Juvenile Sprauge Dawley Mixed litters PND 9/10 4-h post stress PND 9/10 Single exposure to cold stress/3 exposures to cold 1. Increased CRF-mRNA in the central nucleus of the amygdala
Sabatini et al. (2007) 12 Juvenile Rhesus Macaque 4 F 1 week maternally seperated/4F 1 month maternally separated/ 4F controls Infancy equivalent Post stress 3 months 1 week maternally seperated/1 month maternally separated 1. Early separation, more than later separation, decreased amygdala gene expression (guanylate cyclase 1 α 3)
Spinelli et al. (2009) 28 Rhesus monkeys 15 (7M) mother reared/13 (6M) peer reared 0–6 months old Post stress 23–32 Months (age equivalent to childhood) Maternal deprivation 1. No difference in hippocampal volume measurements