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NMDA Neurotransmission As a Critical Mediator of Borderline Personality Disorder

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Specialty Psychiatry
Date 2007 Mar 14
PMID 17353939
Citations 15
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Abstract

Studies of the neurobehavioural components of borderline personality disorder (BPD) have shown that symptoms and behaviours of BPD are partly associated with disruptions in basic neurocognitive processes, in particular, in the executive neurocognition and memory systems. A growing body of data indicates that the glutamatergic system, in particular, the N-methyl-D-aspartate (NMDA) subtype receptor, plays a major role in neuronal plasticity, cognition and memory and may underlie the pathophysiology of multiple psychiatric disorders. In this paper, we review the literature regarding BPD and its cognitive deficits and the current data on glutamatergic and NMDA neurotransmission. We propose that multiple cognitive dysfunctions and symptoms presented by BPD patients, like dissociation, psychosis and impaired nociception, may result from the dysregulation of the NMDA neurotransmission. This impairment may be the result of a combination of biological vulnerability and environmental influences mediated by the NMDA neurotransmission.

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References
1.
Fox K, Daw N, Sato H, Czepita D . Dark-rearing delays the loss of NMDA-receptor function in kitten visual cortex. Nature. 1991; 350(6316):342-4. DOI: 10.1038/350342a0. View

2.
Juengling F, Schmahl C, Hesslinger B, Ebert D, Bremner J, Gostomzyk J . Positron emission tomography in female patients with borderline personality disorder. J Psychiatr Res. 2003; 37(2):109-15. DOI: 10.1016/s0022-3956(02)00084-5. View

3.
Frith U . Mind blindness and the brain in autism. Neuron. 2002; 32(6):969-79. DOI: 10.1016/s0896-6273(01)00552-9. View

4.
Sawamoto N, Honda M, Okada T, Hanakawa T, Kanda M, Fukuyama H . Expectation of pain enhances responses to nonpainful somatosensory stimulation in the anterior cingulate cortex and parietal operculum/posterior insula: an event-related functional magnetic resonance imaging study. J Neurosci. 2000; 20(19):7438-45. PMC: 6772793. View

5.
KERNBERG O . Borderline personality organization. J Am Psychoanal Assoc. 1967; 15(3):641-85. DOI: 10.1177/000306516701500309. View