Regional Changes in Brain Biomolecular Markers in a Collagen-Induced Arthritis Rat Model

Author:

Millen Aletta M. E.12ORCID,Maluleke Tshiamo T.12ORCID,Pienaar Leandrie12,Sallie Farhanah N.12ORCID,Veerappan Radhini12,Andrén Per E.3ORCID,Baijnath Sooraj12ORCID

Affiliation:

1. Wits Integrated Molecular Physiology Research Initiative, Wits Health Consortium (PTY) Ltd., University of the Witwatersrand, Johannesburg 2191, South Africa

2. School of Physiology, Faculty of Health Sciences, University of The Witwatersrand, Johannesburg 2191, South Africa

3. Department of Pharmaceutical Biosciences, Spatial Mass Spectrometry, Science for Life Laboratory, Uppsala University, 75121 Uppsala, Sweden

Abstract

Background: The effects of collagen-induced arthritis (CIA), a model of systemic inflammation, on brain regional molecular markers associated with neurological disorders are uncertain. Objective: This study investigated the brain regional molecular changes in markers associated with inflammation and neuronal dysfunction in a CIA model. Methods: Fourteen male Sprague Dawley rats were divided into control (n = 5) or CIA (n = 9) groups. 10 weeks after CIA induction, brain tissue was collected. Brain regional mRNA expression of inflammatory markers (IL-1β and IL-6), apoptotic markers (BAX and Bcl2) and neurotrophic factors (BDNF, CREB and TrkB) was determined. Monoamine distribution and abundance in different brain regions were determine by mass spectrometry imaging (MSI). Results: Neuroinflammation was confirmed in the CIA group by increased IL-β mRNA expression, concurrent with an increased BAX/Bcl2 ratio. The mRNA expression of CREB was increased in the midbrain and hippocampus while BDNF was increased and TrkB was decreased across all brain regions in CIA compared to control animals. Serotonin was decreased in the midbrain and hippocampus while dopamine was decreased in the striatum of CIA rats, compared to controls. Conclusion: CIA resulted in neuroinflammation concurrent with an apoptotic state and aberrant expression of neurotrophic factors and monoamines in the brain, suggestive of neurodegeneration.

Funder

National Research Foundation

International Brain Research Organization, the University of the Witwatersrand, the Swedish Research Council

Swedish Brain Foundation

Swedish Research Council

Science for Life Laboratory

Publisher

MDPI AG

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