4.5 Article

Neuroprotective Effects of Theobromine in permanent bilateral common carotid artery occlusion rat model of cerebral hypoperfusion

Journal

METABOLIC BRAIN DISEASE
Volume 37, Issue 6, Pages 1787-1801

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11011-022-00995-6

Keywords

Theobromine; Cerebral hypoperfusion; GABA; Inflammation; Memory; Oxidative stress

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This study evaluated the neuroprotective potential of theobromine against cerebral hypoperfusion. The results showed that theobromine could improve neurological deficits, sensorimotor functions, and memory, and attenuate oxidative stress and inflammation in brain tissues. These findings suggest that theobromine may play an important role in improving the pathology of cerebral hypoperfusion.
Cerebral hypoperfusion (CH) is a common underlying mechanism of dementia disorders linked to aberrations in the neurovascular unit. Hemodynamic disturbances adversely affect cellular energy homeostasis that triggers a sequence of events leading to irrevocable damage to the brain and neurobehavioral discrepancies. Theobromine is a common ingredient of many natural foods consumed by a large population worldwide. Theobromine has shown health benefits in several studies, attributed to regulation of calcium homeostasis, phosphodiesterase, neurotransmission, and neurotrophins. The current study evaluated the neuroprotective potential of theobromine against CH in the permanent bilateral common carotid artery occlusion (BCCAO) prototype. Wistar rats were distributed in Sham-operated (S), S + T100, CH, CH + T50, and CH + T100 groups. Animals received permanent BCCAO or Sham treatment on day 1. Theobromine (50, 100 mg/kg) was given orally in animals subjected to BCCAO for 14 days daily. CH caused neurological deficits (12-point scale), motor dysfunction, and memory impairment in rats. Treatment with theobromine significantly attenuated neurological deficits and improved sensorimotor functions and memory in rats with CH. In biochemistry investigation of the entire brain, findings disclosed reduction in brain oxidative stress, inflammatory intermediaries (tumor necrosis factor-alpha, interleukin-1 beta and - 6, nuclear factor-kappa B), markers of cell demise (lactate dehydrogenase, caspase-3), acetylcholinesterase activity, and improvement in gamma-aminobutyric acid quantity in rats that were given theobromine for 14 days daily after CH. Histopathological analysis substantiated attenuation of neurodegenerative changes by theobromine. The findings of this study indicated that theobromine could improve neurological scores, sensorimotor abilities, and memory in CH prototype.

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