BSc (hons) Human Biology.
Msc Neuroscience.
PhD Applied Neuroscience (Neuropharmacology).
Medical writer.
British Neuroscience Association.
International College of Geriatric Psychoneuropharmacology.
Khundakar AA and Thomas AJ. The possible applications (and pitfalls!) of stereological analysis in post-mortem brain research. In Mouton, P (Ed.) Neurostereology. Holboken, New Jersey: Wiley-Blackwell, 2012. In Press
Khundakar A, Zetterström T. Effects of GABA(B) ligands alone and in combination with paroxetine on hippocampal BDNF gene expression. European Journal of Pharmacology 2011, 671(1-3), 33-38.
Khundakar A, Morris C, Oakley A, McMeekin W, Thomas AJ. Morphometric analysis of neuronal and glial cell pathology in the dorsolateral prefrontal cortex in late-life depression. British Journal of Psychiatry 2009, 195(2), 163-169.
2009 IAH 'Excellence with Impact' Award - 1st prize.
2011 International College of Geriatric Psychoneuropharmacology - Junior Researcher Award.
2011 'Evaluating the Vascular Depression Hypothesis: A Review of Cellular Morphometry Studies'; Vascular Dementia Congress October 20-23, Riga, Latvia.
2011 'Morphometric Analysis of Brain Circuitry in Late-Life Depression'; International College of Geriatric Psychoneuropharmacology November 2-5, Irvine, California, US.
My research at the Institute for Ageing and Health (IAH), Newcastle University aimed to elucidate the anatomical correlates of late-life depression by examining morphological cellular changes in post-mortem brain tissue using unbiased three-dimensional stereology. The results acquired from these experiments revealed differential effects of late-life depression on neuronal morphology, dependent on affective area examined. Specifically, significant changes were found in the dorsolateral prefrontal cortex and caudate nucleus, but not orbitofrontal or anterior cingulate cortices, in patients with late-life depression. Intriguingly, no changes were found in glial cell populations in any area examined, contrasting with previous studies in younger depressed patients.
My PhD research in neuropharmacology focused on the mechanistic effect of antidepressant treatment on neurotrophic factors within the rat hippocampus. It was found that a ‘biphasic’ effect occurred on hippocampal brain-derived neurotrophic factor (BDNF) mRNA expression after antidepressant therapy. Acute administration of various antidepressant drugs resulted in inhibition, whereas chronic treatment resulted in an upregulatory effect on BDNF. The initial inhibitory effect on BDNF was discovered to be regulated by gamma-aminobutyric acid (GABA; specifically GABAB) receptor-mediated activation.
Neuropharmacology of depression
The involvement of neurotrophic factors in depression
Medical/scientific writing, proofreading and editing
Dementia with Lewy bodies (DLB) is characterised by recurrent visual hallucinations often leading to disorientation and distress in patients. The lateral geniculate nucleus (LGN) and primary visual cortex (BA17) are first and second neuronal systems after the eyes which process visual information. I am therefore currently examining the possible pathological changes present within the LGN and primary visual cortex in the post-mortem tissue of patients with DLB using stereological and immunohistochemical analysis. This novel study is very important in establishing whether the visual hallucinations experienced in DLB patients are a result of pathological changes in the visual system within the brain, providing a greater understanding of the pathophysiological processes behind DLB.