Literature DB >> 8137151

Alterations in behavioral responses to stressors following excitotoxin lesions of dorsomedial hypothalamic regions.

J R Inglefield1, S B Schwarzkopf, C K Kellogg.   

Abstract

The dorsomedial hypothalamus is important for regulation of cardiovascular responses associated with emotional arousal. This region has also been identified as a component of neural circuitry involved in fear/anxiety, yet clear evidence as to the effects of lesioning on stress-related behaviors is missing. In this study, we lesioned the dorsomedial hypothalamic region with the neurotoxin, ibotenic acid (IBO; 2.0 micrograms in 0.2 microliter), and studied the impact on spontaneous and unlearned behavioral responses to stressors. In the open field test, we observed non-generalized increases in motility parameters in the IBO rats with the differences occurring in the latter two-thirds of the test. In the elevated plus-maze, the IBO rats displayed a classic anxiolytic response with a greater proportion of entries into (and greater time spent in) the open arms of the maze. In the environment-specific social interaction (SI) test, the IBO rats showed a normal familiar/unfamiliar environment discrimination with respect to Total SI; however, the composition of the behaviors ('curiosity' vs. physical contact) by the IBO rats was markedly altered, with there being a 2-fold increase in non-violent physical interactions. Additionally, the differences in these traditional indices of anxiety were associated with lesioned animals exhibiting greater acoustic startle responsiveness than controls as a function of prepulse intensity. Overall, the results following IBO lesions indicate an altered responsiveness to sudden stressors, particularly as relates to novelty or exploration-oriented behaviors. The hypothalamic lesion may, therefore, have resulted in a disinhibition of normally suppressed responding to innate fear or challenging stimuli. This study contributes to those that have begun to define neural interactions that are essential for integrated stress responses.

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Year:  1994        PMID: 8137151     DOI: 10.1016/0006-8993(94)91534-2

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  6 in total

1.  Cerebellar connections to the dorsomedial and posterior nuclei of the hypothalamus in the rat.

Authors:  S Cavdar; T San; R Aker; U Sehirli; F Onat
Journal:  J Anat       Date:  2001-01       Impact factor: 2.610

Review 2.  Cerebellar connections: hypothalamus.

Authors:  Filiz Onat; Safiye Cavdar
Journal:  Cerebellum       Date:  2003       Impact factor: 3.847

3.  Mapping cerebral blood flow changes during auditory-cued conditioned fear in the nontethered, nonrestrained rat.

Authors:  D P Holschneider; J Yang; T R Sadler; P T Nguyen; T K Givrad; J-M I Maarek
Journal:  Neuroimage       Date:  2005-10-10       Impact factor: 6.556

4.  Hypothalamic GABAA receptor blockade modulates cerebral cortical systems sensitive to acute stressors.

Authors:  J R Inglefield; C K Kellogg
Journal:  Psychopharmacology (Berl)       Date:  1994-11       Impact factor: 4.530

5.  Estrogen-related receptor β deficiency alters body composition and response to restraint stress.

Authors:  Mardi S Byerly; Roy D Swanson; G William Wong; Seth Blackshaw
Journal:  BMC Physiol       Date:  2013-09-22

6.  Inhibitory function of the dorsomedial hypothalamic nucleus on the hypothalamic-pituitary-adrenal axis response to an emotional stressor but not immune challenge.

Authors:  K Ebner; P Muigg; N Singewald
Journal:  J Neuroendocrinol       Date:  2013-01       Impact factor: 3.627

  6 in total

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