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Biological psychology proposes that aggression has physiological underpinnings involving specific brain structures, neurotransmitters, and hormones. This lesson examines the roles of the limbic system (particularly the amygdala and hypothalamus), the neurotransmitter serotonin, and the hormone testosterone in explaining aggressive behaviour. Throughout, we consider the strengths and limitations of biological explanations.
Key Definition: Aggression is behaviour directed towards another individual with the intention of causing harm. It may be hostile (driven by anger, aimed at causing pain) or instrumental (goal-directed, a means to achieve an objective).
The limbic system is a group of interconnected brain structures located deep within the temporal lobes and beneath the cortex. It plays a central role in emotional processing, motivation, and behaviour — including aggression.
The two structures most strongly implicated in aggression are the amygdala and the hypothalamus.
The amygdala is an almond-shaped structure in the temporal lobe. It is involved in processing emotions — particularly fear and aggression — and in the formation of emotional memories.
Evidence from animal studies:
Evidence from human studies:
The hypothalamus is a small structure at the base of the brain that regulates the autonomic nervous system and the endocrine system. It plays a key role in the fight-or-flight response and has been linked to both reactive and predatory aggression.
Key Definition: The limbic system includes the amygdala, hypothalamus, hippocampus, and other structures involved in emotion, motivation, and behaviour. The amygdala processes fear and aggression; the hypothalamus coordinates the fight-or-flight response.
Serotonin (5-HT) is a neurotransmitter involved in mood regulation, sleep, appetite, and impulse control. Research consistently shows that low levels of serotonin are associated with increased impulsive aggression.
Serotonin has an inhibitory effect on aggressive behaviour. It acts in the prefrontal cortex to regulate impulsive and aggressive responses. When serotonin levels are low, the prefrontal cortex is less able to exert control over the limbic system (particularly the amygdala), resulting in disinhibited aggressive behaviour.
Mann et al. (1990) administered dexfenfluramine — a drug that depletes serotonin levels — to 35 healthy participants. They found that the drug produced increased hostility and aggression scores on questionnaire measures, particularly in males. This supports the idea that reduced serotonin is directly linked to increased aggression.
Linnoila and Virkkunen (1992) studied Finnish males imprisoned for violent crimes. They found that those who had committed impulsive violent acts (e.g., unplanned assaults) had significantly lower levels of the serotonin metabolite 5-HIAA in their cerebrospinal fluid (CSF) compared with those who had committed premeditated violence. This suggests that serotonin deficiency is specifically linked to impulsive rather than planned aggression.
Berman et al. (2009) conducted an experimental study in which participants given a serotonin-enhancing drug (paroxetine, an SSRI) showed reduced aggressive responses in a laboratory aggression task, compared with those given a placebo. This further supports a causal role for serotonin in modulating aggression.
| Study | Method | Key Finding |
|---|---|---|
| Mann et al. (1990) | Dexfenfluramine challenge in healthy participants | Low serotonin → increased hostility |
| Linnoila & Virkkunen (1992) | CSF analysis of violent offenders | Low 5-HIAA → impulsive violence |
| Berman et al. (2009) | SSRI administration in lab aggression task | Increased serotonin → reduced aggression |
Strengths:
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