behaviorally inhibited monkeys demonstrate less coo calls...

1
Glucose Glucose Glucose Glucose Glucose Glucose Glucose 18-FDG Glucose Glucose Glucose Glucose Glucose Glucose Glucose Glucose 18-FDG 18-FDG Glucose Glucose Glucose Glucose Glucose Glucose Glucose Glucose 18-FDG 18-FDG Glucose Glucose Glucose Glucose Glucose Glucose Glucose Glucose 18-FDG 18-FDG Glucose 6P-FDG 6P-G Phosphorylation Glycolysis Energy 18-FDG Glucose 6P-FDG 6P-G Phosphorylation Glycolysis Energy OH HO OH O F HO + 18-F 18-O + 18-F * * + * * + * * + S e n s o r S e n s o r S e n s o r P E T S c a n ne r Behaviorally inhibited monkeys demonstrate less coo calls and more amygdala activation during separation 72.20/EE20 Departments of Psychology 1 , and Psychiatry 2 , and the Waisman Laboratory for Brain Imaging and Behavior 3 , at the Universtiy of Wisconsin-Madison A.S.Fox 1,3* , S.E.Shelton 2 , T.R.Oakes 3 , A.K.Converse 3 , R.J.Davidson 1,2,3 , N.H.Kalin 2,3 Behavioral Inhibition Vocalizations Amygdala Cortisol Time Intensity Individual 1 Individual 2 Time Intensity Individual 1 Individual 2 L R -3 -2 -1 0 1 2 3 -2.5 -2 -1.5 -1 -0.5 0 0.5 1 1.5 2 2.5 Common Amygdala Region Area 10 -3 -2 -1 0 1 2 3 Right Area 46 -3 -2 -1 0 1 2 3 Left Area 46 Extreme behavioral inhibition in childhood is a risk factor for the development of anxiety and affec- tive disorders (Fox NA et al., 2005). Individual differences in behavioral inhibition during childhood have been linked to increased cortisol levels (Buss et al., 2004), and increased amygdala respon- siveness to novelty in early adulthood (Schwartz et al., 2003). Moreover, work in rhesus monkeys demonstrated the amygdala to be involved in behavioral inhibition by using selective lesioning techniques (Emery et al., 2001; Kalin et al, 2004). Using Positron Emission Tomography (PET) im- aging in rhesus monkeys, our group observed individual differences in behavioral inhibition to be positively correlated with amygdala activity whereas individual differences in separation-induced cooing, or calling for help, were negatively correlated with amygdala activity (Fox AS et al., 2005). In the present study, we used high-resolution PET scanning in freely behaving rhesus monkeys to further examine amygdala activity in relation to extreme behavioral inhibition, cooing and plasma cortisol levels during separation. Area 46/9 Area 10 -1 -0.8 -0.6 -0.4 -0.2 0 0.2 0.4 0.6 0.8 1 Low Med High Common Amygdala Region -3 -2 -1 0 1 2 3 -2.5 -2 -1.5 -1 -0.5 0 0.5 1 1.5 2 2.5 Cortisol Common Amygdala Region -3 -2 -1 0 1 2 3 -2.5 -2 -1.5 -1 -0.5 0 0.5 1 1.5 2 2.5 Common Amygdala Region Cooing Anterior Posterior L R L R Positive Correlation with Cortisol in the Right Amygdala High > Med Right Amygdala Negative Correlation with Cooing in the Right Amygdala The amygdala was significantly (p<.005, one-tailed uncor- rected) more activated in the high group (n=11) when com- pared to the medium group (n=12) during separation (p=.002). The amygdala was significantly (p<.005, one-tailed uncorrected; n=35) positively correlated with plasma cortisol levels obtained following the behavioral para- digm (R 2 =.168). The amygdala was significantly (p<.005, one-tailed un- corrected; n=35) negatively correlated with affiliative, coo vocalizations emitted during separation (R 2 =-.271). While it has been suggested that behavioral inhibition may in part be due to alterations in self-regulation, no research has explored the neural basis for alterations in the regula- tion of emotion hypothesized to underlie behavioral inhibi- tion. Recent evidence suggests that the projections from the ventral-medial prefrontal cortex (VMPFC) to the amyg- dala may in part underlie the ability to regulate fear and anxiety related responses (Quirk et al., 2000; Quirk et al., 2003; Kim et al., 2004; Urry et al., 2006). The initiation of the VMPFC regulatory effects has been further suggested to involve the recruitment of dorsal-lateral prefrontal cortex (DLPFC; areas 46/9) and the anterior frontal pole (Area 10) (Davidson, Fox, & Kalin, in press; Johnstone et al., submitted; Kim et al., 2004; Urry et al., 2005). A logical AND conjunction analysis within the amyg- dala revealed a significant (p<.005, one-tailed uncor- rected) region of the amygdala which differed be- tween the high and middle behavioral inhibition groups and was negatively correlated with the fre- quency of coo vocalizations, and positively corre- lated with cortisol. Three groups of monkeys (High n=11; Med n=12; Low n=12) were selected from 117 ani- mals based on their propensity to be stably be- haviorally inhibited, as measured by their amount of freezing when presented with the profile of a human intruder (Kalin & Shelton, 1989). Behavioral analyses for the behaviors occur- ring during the period of FDG uptake demon- strated significant differences across the be- havioral inhibition groups in freezing (F=5.585, p=.009) and cooing (F=8.924, p=.001) during separation. There were no significant differ- ences between groups in plasma cortisol levels when sampled immediately after the separation paradigm (F=1.199, p=.316). Preprocessing of Imaging Data MRI images were transformed into standard space and segmented according to standardized analysis protocols. First, non-brain tissues were manually masked (i.e. set to zero) in all the MRI images. Masked MRI images were regis- tered to a rhesus monkey template described in Fox et al. and Kalin et al., using a 60-parameter nonlinear registration as implemented in the AIR software package (A. S. Fox et al., 2005; Kalin et al., 2005; Woods et al., 1998). Finally, MRI images were segmented using a probabilistic segmentation algorithm, FSL (Zhang, Brady & Smith, 2001). The segmenta- tion process created an image for each subject where the value of each voxel represented the probability of gray matter for that voxel. To facilitate across subject comparisons PET scans were transformed according to the MRI images using standard methods (Worsley et al., 2002; Kalin et al., 2005). Specifically, FDG-PET scans were co-registered using a 6-parameter rigid body registration to the anatomical MRI image taken from the same subject using the mutual information algorithm implemented by FSL (Jenkinson and Smith, 2001). The transformations computed based on the MRI images were then applied to the FDG-PET images resulting in individual FDG-PET scans in a standard space. To facilitate inter subject comparisons, each FDG image was intensity normalized prior to statistical analyses. Intensity normalization was performed based on a global scale factor determined by adjusting the mean based on whole-brain intensity values using standard analysis techniques (Carmargo et al., 1992). Statistical Analyses Group comparisons were performed between the highly behaviorally inhibited group and the middle group exam- ining differences in cooing and vocalizations as well as brain metabolism during separation. Group comparisons based on References Buss K. A., et al. (2004). Developmental Psychology, 40(4), 583-594. Davidson R.J., et al. (in press). In J. Gross (Ed.), Handbook of Emotion Regulation . New York: Guildford Press. Emery N. J., et al. (2001). Behavioral Neuroscience, 115(3), 515-544. Fox A. S., et al. (2005). Proc Nat Acad Sci USA, 102(11), 4176-4179. Fox N. A., et al. (2005). Ann Rev Psych, 56, 235-262. Jenkinson M., & Smith S. (2001). Med Image Anal. 5(2):143-56. Johnstone T., et al. (Submitted) Kalin N. H., & Shelton, S. E. (1989). Science, 243(4899), 1718-1721. Kalin N. H., et al. (2004). Journal of Neuroscience, 24(24), 5506-5515. Kalin N. H., et al. (2005) Biological Psychiatry, 58(10), 796-804. This work was suppported by the HealthEmotions Research Institute, Meriter Hospita, and NIH Grants MH46729 and MH69315. We would like to thank T Johnstone, A Shackman, H Van Valkenberg, T Johnson, and the staff at the Harlow Center for Biological Psychology and the National Primate Research Center at the University of Wisconsin for their technical support. brain metabolism were performed on a whole-brain voxelwise basis. Correlations were performed between brain metabo- lism and the frequency of cooing occurring during the separation period and with cortisol levels assessed from samples collected immediately after the separation period. All statistical comparisons involving brain metabolism were performed on a voxelwise basis statistically controlling for age and gray-matter probability, to control for differences in anatomy (Oakes et al., in press; Worsley et al., 1998). To investigate the common neural mechanisms that underlie different facets of behavioral inhibition (i.e. group, cooing, and cortisol), a conjunction analysis was performed using a logical AND conjunc- tion (Nichols, et al., 2005). The conjunction analysis was performed at the p<.005, one-tailed uncorrected threshold on a voxelwise basis within the amygdala. The relationship between amygdala activity with the rest of the brain in the highly inhibited group was compared with that in the other groups. This was done by computing a voxelwise regression between the amygdala and the rest of the brain in the middle group after statistically controlling for age and gray-matter probability (Oakes et al., in press; Worsley et al., 1998). After identifying the regions that were significantly negatively correlated with the amygdala we examined the highly inhibited group to determine the correlations between the amygdala and the same areas to see if the highly behavior- ally inhibited monkeys showed a different relationship. This was done by extracting the regression coefficients attributable to the amygdala and their standard deviations at each voxel in both the highly behaviorally inhibited and the middle groups. Resulting regression coefficients were compared to each other using standard multiple regression techniques (Cohen et al., 2003). The resulting statistical parametric map of t-values tested the null hypothesis at each voxel that the two groups had equivalent correlations between that voxel and the amygdala. Results in the Right Amygdala Results demonstrated Areas 46/9 and 10 to be significantly (p<.005, one-tailed uncorrected) nega- tively associated with amygdala in the middle group (n=12; Right-R 2 =-.660, Left R 2 =-.663). Further analyses revealed these areas to show a significantly (p<.005, one-tailed uncorrected) greater negative correlation than the high group (n=11; Right-R 2 =.218, Left-R 2 =.199). Regulation Results Emotion Regulation Kim H, et al. (2004). Journal of Cognitive Neuroscience, 16(10), 1730-1745. Nichols T. et al., (2005). Neuroimage, 25(3):653-60. Oakes T. R., et al. (In Press) Neuroimage. Quirk G. J., et al. (2003). Journal of Neuroscience, 23, 8800-8807. Quirk G. J., et al. (2000). Journal of Neuroscience, 20, 6225-31. Schwartz C. E. et al., (2003) Science, 300(5627), 1952-1953. Urry H. L. et al., (2006) Journal of Neuroscience, 26(16), 4415-4425. Woods RP, et al. (1998) J Comput Assist Tomogr 22:153-165. Worsley KJ, et al. (2002). NeuroImage, 15:1:15. Worsley KJ, et al. (1998). NeuroImage , 6:305-319. 2.65 2.7 2.75 2.8 2.85 2.9 2.95 3 ALN ALN NEC NEC High igh Med ed -1 -0.8 -0.6 -0.4 -0.2 0 0.2 0.4 0.6 0.8 1 Low Med High Cooing + SE(Men) LOW MED HIGH LOW MED HIGH 0 50 100 150 200 250 300 350 400 450 Low Med High Behavioral Inhibition Group Freezing + SE(Mean) Screening 1 Screening 2 Definition of Groups FDG PET Paradigm Behavioral Paradigm 0 min. Injection of Radiotracer 20 min. 40 min. Anesthisia Injection Transportation Begin PET Scan 10 min. 30 min. ~50 min. FDG in the Brain After identification of the 3 groups of animals, each monkey underwent a [18F]-fluoro-2- deoxy-D-glucose (FDG) PET scan to investi- gate the integrated neural activity associated with separation from their partner into a test cage. FDG was administered immediately prior to the 30 min separation period after which the monkeys were anesthetized and scanned. Behavioral Analysis FDG PET Methods These results suggest that during social separation heightened amygdala activity is associated with excessive behavioral inhibition and decreased attempts to call for help. Furthermore, the relation- ship between amygdala activity and prefrontal cortex activity may underlie individual differences in the ability to appropriately regulate behavioral inhibition. Increased amygdala activity in behaviorally inhibited individuals may impair their ability to recruit social support during periods of stress which could be related to their increased risk to develop anxiety and depression. Discussion Introduction

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Behaviorally inhibited monkeys demonstrate less coo calls and more amygdala activation during separation

72.20/EE20

Departments of Psychology1, and Psychiatry2, and the Waisman Laboratory for Brain Imaging and Behavior3, at the Universtiy of Wisconsin-Madison

A.S.Fox1,3*, S.E.Shelton2, T.R.Oakes3, A.K.Converse3, R.J.Davidson1,2,3, N.H.Kalin2,3

Behavioral Inhibition

Vocalizations

Amygdala Cortisol

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Individual 1Individual 2

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Extreme behavioral inhibition in childhood is a risk factor for the development of anxiety and affec-tive disorders (Fox NA et al., 2005). Individual differences in behavioral inhibition during childhood have been linked to increased cortisol levels (Buss et al., 2004), and increased amygdala respon-siveness to novelty in early adulthood (Schwartz et al., 2003). Moreover, work in rhesus monkeys demonstrated the amygdala to be involved in behavioral inhibition by using selective lesioning techniques (Emery et al., 2001; Kalin et al, 2004). Using Positron Emission Tomography (PET) im-aging in rhesus monkeys, our group observed individual differences in behavioral inhibition to be positively correlated with amygdala activity whereas individual differences in separation-induced cooing, or calling for help, were negatively correlated with amygdala activity (Fox AS et al., 2005). In the present study, we used high-resolution PET scanning in freely behaving rhesus monkeys to further examine amygdala activity in relation to extreme behavioral inhibition, cooing and plasma cortisol levels during separation.

Area 46/9

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Positive Correlation with Cortisol in the Right Amygdala

High > Med Right Amygdala

Negative Correlation with Cooing in the Right Amygdala

The amygdala was significantly (p<.005, one-tailed uncor-rected) more activated in the high group (n=11) when com-pared to the medium group (n=12) during separation (p=.002).

The amygdala was significantly (p<.005, one-tailed uncorrected; n=35) positively correlated with plasma cortisol levels obtained following the behavioral para-digm (R2=.168).

The amygdala was significantly (p<.005, one-tailed un-corrected; n=35) negatively correlated with affiliative, coo vocalizations emitted during separation (R2=-.271).

While it has been suggested that behavioral inhibition may in part be due to alterations in self-regulation, no research has explored the neural basis for alterations in the regula-tion of emotion hypothesized to underlie behavioral inhibi-tion. Recent evidence suggests that the projections from the ventral-medial prefrontal cortex (VMPFC) to the amyg-dala may in part underlie the ability to regulate fear and anxiety related responses (Quirk et al., 2000; Quirk et al., 2003; Kim et al., 2004; Urry et al., 2006). The initiation of the VMPFC regulatory effects has been further suggested to involve the recruitment of dorsal-lateral prefrontal cortex (DLPFC; areas 46/9) and the anterior frontal pole (Area 10) (Davidson, Fox, & Kalin, in press; Johnstone et al., submitted; Kim et al., 2004; Urry et al., 2005).

A logical AND conjunction analysis within the amyg-dala revealed a significant (p<.005, one-tailed uncor-rected) region of the amygdala which differed be-tween the high and middle behavioral inhibition groups and was negatively correlated with the fre-quency of coo vocalizations, and positively corre-lated with cortisol.

Three groups of monkeys (High n=11; Med n=12; Low n=12) were selected from 117 ani-mals based on their propensity to be stably be-haviorally inhibited, as measured by their amount of freezing when presented with the profile of a human intruder (Kalin & Shelton, 1989).

Behavioral analyses for the behaviors occur-ring during the period of FDG uptake demon-strated significant differences across the be-havioral inhibition groups in freezing (F=5.585, p=.009) and cooing (F=8.924, p=.001) during separation. There were no significant differ-ences between groups in plasma cortisol levels when sampled immediately after the separation paradigm (F=1.199, p=.316).

Preprocessing of Imaging Data

MRI images were transformed into standard space and segmented according to standardized analysis protocols.

First, non-brain tissues were manually masked (i.e. set to zero) in all the MRI images. Masked MRI images were regis-

tered to a rhesus monkey template described in Fox et al. and Kalin et al., using a 60-parameter nonlinear registration as

implemented in the AIR software package (A. S. Fox et al., 2005; Kalin et al., 2005; Woods et al., 1998). Finally, MRI

images were segmented using a probabilistic segmentation algorithm, FSL (Zhang, Brady & Smith, 2001). The segmenta-

tion process created an image for each subject where the value of each voxel represented the probability of gray matter for

that voxel.

To facilitate across subject comparisons PET scans were transformed according to the MRI images using standard

methods (Worsley et al., 2002; Kalin et al., 2005). Specifically, FDG-PET scans were co-registered using a 6-parameter

rigid body registration to the anatomical MRI image taken from the same subject using the mutual information algorithm

implemented by FSL (Jenkinson and Smith, 2001). The transformations computed based on the MRI images were then

applied to the FDG-PET images resulting in individual FDG-PET scans in a standard space. To facilitate inter subject

comparisons, each FDG image was intensity normalized prior to statistical analyses. Intensity normalization was

performed based on a global scale factor determined by adjusting the mean based on whole-brain intensity values using

standard analysis techniques (Carmargo et al., 1992).

Statistical Analyses

Group comparisons were performed between the highly behaviorally inhibited group and the middle group exam-

ining differences in cooing and vocalizations as well as brain metabolism during separation. Group comparisons based on

ReferencesBuss K. A., et al. (2004). Developmental Psychology, 40(4), 583-594. Davidson R.J., et al. (in press). In J. Gross (Ed.), Handbook of Emotion

Regulation . New York: Guildford Press. Emery N. J., et al. (2001). Behavioral Neuroscience, 115(3), 515-544. Fox A. S., et al. (2005). Proc Nat Acad Sci USA, 102(11), 4176-4179. Fox N. A., et al. (2005). Ann Rev Psych, 56, 235-262. Jenkinson M., & Smith S. (2001). Med Image Anal. 5(2):143-56.Johnstone T., et al. (Submitted)Kalin N. H., & Shelton, S. E. (1989). Science, 243(4899), 1718-1721. Kalin N. H., et al. (2004). Journal of Neuroscience, 24(24), 5506-5515. Kalin N. H., et al. (2005) Biological Psychiatry, 58(10), 796-804.

This work was suppported by the HealthEmotions Research Institute, Meriter Hospita, and NIH Grants MH46729 and MH69315. We would like to thank T Johnstone, A Shackman, H Van Valkenberg, T Johnson, and the staff at the Harlow Center for Biological Psychology and the National Primate Research Center at the University of Wisconsin for their technical support.

brain metabolism were performed on a whole-brain voxelwise basis. Correlations were performed between brain metabo-

lism and the frequency of cooing occurring during the separation period and with cortisol levels assessed from samples

collected immediately after the separation period. All statistical comparisons involving brain metabolism were performed

on a voxelwise basis statistically controlling for age and gray-matter probability, to control for differences in anatomy

(Oakes et al., in press; Worsley et al., 1998). To investigate the common neural mechanisms that underlie different facets of

behavioral inhibition (i.e. group, cooing, and cortisol), a conjunction analysis was performed using a logical AND conjunc-

tion (Nichols, et al., 2005). The conjunction analysis was performed at the p<.005, one-tailed uncorrected threshold on a

voxelwise basis within the amygdala.

The relationship between amygdala activity with the rest of the brain in the highly inhibited group was compared

with that in the other groups. This was done by computing a voxelwise regression between the amygdala and the rest of the

brain in the middle group after statistically controlling for age and gray-matter probability (Oakes et al., in press; Worsley

et al., 1998). After identifying the regions that were significantly negatively correlated with the amygdala we examined the

highly inhibited group to determine the correlations between the amygdala and the same areas to see if the highly behavior-

ally inhibited monkeys showed a different relationship. This was done by extracting the regression coefficients attributable

to the amygdala and their standard deviations at each voxel in both the highly behaviorally inhibited and the middle groups.

Resulting regression coefficients were compared to each other using standard multiple regression techniques (Cohen et al.,

2003). The resulting statistical parametric map of t-values tested the null hypothesis at each voxel that the two groups had

equivalent correlations between that voxel and the amygdala.

Results in the Right Amygdala

Results demonstrated Areas 46/9 and 10 to be significantly (p<.005, one-tailed uncorrected) nega-tively associated with amygdala in the middle group (n=12; Right-R2=-.660, Left R2=-.663). Further analyses revealed these areas to show a significantly (p<.005, one-tailed uncorrected) greater negative correlation than the high group (n=11; Right-R2=.218, Left-R2=.199).

Regulation Results

Emotion Regulation

Kim H, et al. (2004). Journal of Cognitive Neuroscience, 16(10), 1730-1745.Nichols T. et al., (2005). Neuroimage, 25(3):653-60.Oakes T. R., et al. (In Press) Neuroimage.Quirk G. J., et al. (2003). Journal of Neuroscience, 23, 8800-8807. Quirk G. J., et al. (2000). Journal of Neuroscience, 20, 6225-31. Schwartz C. E. et al., (2003) Science, 300(5627), 1952-1953. Urry H. L. et al., (2006) Journal of Neuroscience, 26(16), 4415-4425. Woods RP, et al. (1998) J Comput Assist Tomogr 22:153-165.Worsley KJ, et al. (2002). NeuroImage, 15:1:15.Worsley KJ, et al. (1998). NeuroImage , 6:305-319.

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Screening 1 Screening 2

Definition of Groups

FDG PET Paradigm

Behavioral Paradigm

0 min.

Injection of Radiotracer

20 min. 40 min.

AnesthisiaInjection

Transportation

BeginPET Scan

10 min. 30 min. ~50 min.

FDG in theBrain

After identification of the 3 groups of animals, each monkey underwent a [18F]-fluoro-2-deoxy-D-glucose (FDG) PET scan to investi-gate the integrated neural activity associated with separation from their partner into a test cage. FDG was administered immediately prior to the 30 min separation period after which the monkeys were anesthetized and scanned.

Behavioral Analysis

FDG PET Methods

These results suggest that during social separation heightened amygdala activity is associated with excessive behavioral inhibition and decreased attempts to call for help. Furthermore, the relation-ship between amygdala activity and prefrontal cortex activity may underlie individual differences in the ability to appropriately regulate behavioral inhibition. Increased amygdala activity in behaviorally inhibited individuals may impair their ability to recruit social support during periods of stress which could be related to their increased risk to develop anxiety and depression.

Discussion

Introduction