Literature DB >> 12270692

Disruption of the blood-brain barrier and neuronal cell death in cingulate cortex, dentate gyrus, thalamus, and hypothalamus in a rat model of Gulf-War syndrome.

Ali Abdel-Rahman1, Ashok K Shetty, Mohamed B Abou-Donia.   

Abstract

We investigated the effects of a combined exposure to restraint stress and low doses of chemicals pyridostigmine bromide (PB), N, N-diethyl-m-toluamide (DEET), and permethrin in adult male rats, a model of Gulf-War syndrome. Animals were exposed daily to one of the following for 28 days: (i) a combination of stress and chemicals (PB, 1.3 mg/kg/day; DEET, 40 mg/kg/day; and permethrin, 0.13 mg/kg/day); (ii) stress and vehicle; (iii) chemicals alone; and (iv) vehicle alone. All animals were evaluated for: (i) the disruption of the blood-brain barrier (BBB) using intravenous horseradish peroxidase (HRP) injections and endothelial barrier antigen (EBA) immunostaining; (ii) neuronal cell death using H&E staining, silver staining, and glial fibrillary acidic protein (GFAP) immunostaining; and (iii) acetylcholinesterase (AChE) activity and m2-muscarinic acetylcholine receptors (m2-AChR). Animals subjected to stress and chemicals exhibited both disruption of the BBB and neuronal cell death in the cingulate cortex, the dentate gyrus, the thalamus, and the hypothalamus. Other regions of the brain, although they demonstrated some neuronal cell death, did not exhibit disruption of the BBB. The neuropathological changes in the above four brain regions were highly conspicuous and revealed by a large number of HRP-positive neurons (21-40% of total neurons), a decreased EBA immunostaining (42-51% reduction), a decreased number of surviving neurons (27-40% reduction), the presence of dying neurons (4-10% of total neurons), and an increased GFAP immunostaining (45-51% increase). These changes were also associated with decreased forebrain AChE activity and m2-AchR (19-25% reduction). In contrast, in animals exposed to stress and vehicle or chemicals alone, the above indices were mostly comparable to that of animals exposed to vehicle alone. Thus, a combined exposure to stress and low doses of PB, DEET, and permethrin leads to significant brain injury. The various neurological symptoms reported by Gulf-War veterans could be linked to this kind of brain injury incurred during the war.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12270692     DOI: 10.1006/nbdi.2002.0524

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  44 in total

1.  Subcortical brain atrophy in Gulf War Illness.

Authors:  Peka Christova; Lisa M James; Brian E Engdahl; Scott M Lewis; Adam F Carpenter; Apostolos P Georgopoulos
Journal:  Exp Brain Res       Date:  2017-06-20       Impact factor: 1.972

Review 2.  Muscarinic receptors: their distribution and function in body systems, and the implications for treating overactive bladder.

Authors:  Paul Abrams; Karl-Erik Andersson; Jerry J Buccafusco; Christopher Chapple; William Chet de Groat; Alison D Fryer; Gary Kay; Alan Laties; Neil M Nathanson; Pankaj Jay Pasricha; Alan J Wein
Journal:  Br J Pharmacol       Date:  2006-06-05       Impact factor: 8.739

3.  Human lupus autoantibodies against NMDA receptors mediate cognitive impairment.

Authors:  Czeslawa Kowal; Lorraine A Degiorgio; Ji Y Lee; Mark A Edgar; Patricio T Huerta; Bruce T Volpe; Betty Diamond
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-14       Impact factor: 11.205

4.  Mood and memory deficits in a model of Gulf War illness are linked with reduced neurogenesis, partial neuron loss, and mild inflammation in the hippocampus.

Authors:  Vipan K Parihar; Bharathi Hattiangady; Bing Shuai; Ashok K Shetty
Journal:  Neuropsychopharmacology       Date:  2013-06-28       Impact factor: 7.853

5.  Proteomic CNS profile of delayed cognitive impairment in mice exposed to Gulf War agents.

Authors:  Laila Abdullah; Gogce Crynen; Jon Reed; Alex Bishop; John Phillips; Scott Ferguson; Benoit Mouzon; Myles Mullan; Venkatarajan Mathura; Michael Mullan; Ghania Ait-Ghezala; Fiona Crawford
Journal:  Neuromolecular Med       Date:  2011-10-11       Impact factor: 3.843

6.  Anxiety, neuroinflammation, cholinergic and GABAergic abnormalities are early markers of Gulf War illness in a mouse model of the disease.

Authors:  Isabel Carreras; Nurgul Aytan; Tiffany Mellott; Ji-Kyung Choi; Margaret Lehar; Leah Crabtree; Kimberly Leite-Morris; Bruce G Jenkins; Jan Krzysztof Blusztajn; Alpaslan Dedeoglu
Journal:  Brain Res       Date:  2017-12-24       Impact factor: 3.252

7.  Stress does not increase blood-brain barrier permeability in mice.

Authors:  Martin Roszkowski; Johannes Bohacek
Journal:  J Cereb Blood Flow Metab       Date:  2016-05-04       Impact factor: 6.200

8.  Peripheral ChE inhibition modulates brain monoamines levels and c-fos oncogene in mice subjected to a stress situation.

Authors:  L Taysse; D Christin; S Delamanche; B Bellier; P Breton
Journal:  Neurochem Res       Date:  2005-03       Impact factor: 3.996

Review 9.  Blood-brain barrier permeation and efflux exclusion of anticholinergics used in the treatment of overactive bladder.

Authors:  Michael B Chancellor; David R Staskin; Gary G Kay; Bobby W Sandage; Michael G Oefelein; Jack W Tsao
Journal:  Drugs Aging       Date:  2012-04-01       Impact factor: 3.923

10.  A Panel of Autoantibodies Against Neural Proteins as Peripheral Biomarker for Pesticide-Induced Neurotoxicity.

Authors:  Heba Allah Abd El Rahman; Mohamed Salama; Seham A Gad El-Hak; Mona A El-Harouny; Passent ElKafrawy; Mohamed B Abou-Donia
Journal:  Neurotox Res       Date:  2017-09-05       Impact factor: 3.911

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.