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Abstract

This study was done to further analyze the neural mechanisms underlying aggressive behavior associated with psychomotor or temporal lobe seizures. The studies revealed that superkindling the aggressive system by sequential stimulations at seizureinducing thresholds, of two or more sites in the limbic, hypothalamic, and basal ganglia structures facilitated the production of aggressive seizures. Aggressive behavior in the freely moving cat was evaluated in relation to the occurrence of hissing and growling during stimulation, after-discharge and postictal period. The behavior was correlated with the frequency of the elicited seizures and the seizure durations. Aggression did develop as a component behavioral manifestation of the limbic (psychomotor) seizure. Development of aggressive seizures was facilitated by “priming” the aggressive system. Optimum levels of aggressive behavior occurred with seizures of medium duration. Catecholamine blockers tended to attentuate the occurrence of aggression, whereas the agonist tended to facilitate it. Once the aggressive system was rendered hyperexcitable, exteroceptive stimuli also evoked aggressive attack behavior. It was concluded that repeatedly recurring limbic system seizures through superkindling mechanisms can eventually render the limbic-basal ganglia-preoptico-hypothalamic aggressive system hyper-responsive to both recurring seizures and to exteroceptive stimuli with resulting aggressive behavior with or without an accompanying seizure.

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Abbreviations

AA:

anterior amygdaloid area

AC:

nucleus accumbeus

AD:

anterior dorsal nucleus

AM:

anterior medial nucleus

AV:

anterior ventral nucleus

BA:

basalis amygdala

C:

bed nucleus of anterior commissure

CA:

anterior commissure

CA:

centralis amygdala (Fig. 4)

CC:

corpus callosum

CH:

optic chiasm

CL:

claustrum

CN:

caudate nucleus

CO:

corticalis amygdala

DA:

nucleus dorsalis anterior-septum

DB:

nucleus diagonal band of broca

DE:

nucleus dorsalis externa-septum

DM:

nucleus dorsalis intermedius-septum

DM:

dorsomedial nucleus-hypothalamus

EN:

nucleus en-topeduncularis

F:

fimbria

FX:

fornix

GF:

gyrus fornicatus

GG:

gyrus genualis

GR:

gyrus rostralis

GP:

globus pallidus

H:

hippocampus

HA:

anterior hypothalamus

HL:

lateral hypothalamus

HVM:

ventromedial nucleus-hypothalamus

IC:

internal capsule

L:

nucleus lateralis-septum

LA:

lateralis amygdala (Fig. 4)

LA:

left amygdala

LAH:

left amygdala-hippocampus

LENTO:

left en-topeduncular nucleus-tractus opticus

LGPHA:

left globus pallidus-hippocampus-amygdala

LGPOT:

left globus pallidus-optic tract

LHy:

left hypothalamus

LIC:

left internal capsule

LOrC:

left orbital cortex

LPO:

left preoptic area

LS:

left septum

LSTh:

left septum-thalamus

M:

nucleus medialis-septum

MA:

medialis amygdala

MP:

nucleus medialis posterior-septum

NTO:

nucleus of the olfactory tract

NPA:

nucleus paraventricularis

OT:

optic tract

P:

putamen (Fig. 4)

P:

peduncle

Pir:

piriform cortex

PV:

periventricular nucleus

R:

reticular nucleus

RA:

right amygdala

RAEnC:

right amygdala-entrohinal cortex

RAGPP:

right amygdala-globus pallidus-putamen

RAH:

right amgydala-hippocampus

RAPeC:

right amygdalaperiamygdaloid cortex

RCG:

right cingulate gyrus

RCN:

right caudate nucleus

RCNS:

right caudate nucleus-septum

RE:

nucleus reunions

RGPOT:

right globus pallidus-optic tract

RGPP:

right globus pallidus-putamen

RGPr:

right gyrus proreus

RGR:

right gyrus rostralis

RHy:

right hypothalamus

RLHy:

right lateral hypothalamus

RPO:

right preoptic area

RPOS:

right preoptic-septum

RS:

right septum

RSCN:

right septum-caudate nucleus

RSTh:

right septum-thalamus

SCH:

suprachias-matic nucleus

SO:

supraoptic nucleus

ST:

stria terminalis

TMT:

mamillothalamic tract

TE:

bed nucleus of stria terminalis

V:

ventricle

VL:

ventrolateral nucleus

VM:

ventromedial nucleus

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Andy, O.J., Velamati, S. Limbic system seizures and aggressive behavior (superkindling effects). Pay. J. Biol. Sci. 13, 251–264 (1978). https://doi.org/10.1007/BF03002262

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