Prepubertal Repeated Berberine Supplementation Enhances Cerebrocerebellar Functions by Modulating Neurochemical and

Solomon Owumi1, Joseph Chimezie2, Moses Otunla3

  • 1Cancer Research and Molecular Biology Laboratory, Department of Biochemistry, University of Ibadan, Ibadan, 200005, Oyo State, Nigeria. owumisa@hotmail.com.

Insights

Berberine (BER) supplementation enhanced cerebrocerebellar function in prepubertal rats by improving motor behavior and increasing antioxidant enzyme activity. BER also reduced oxidative stress and inflammation, suggesting neuroprotective effects.

Area of Science:

  • Neuroscience
  • Pharmacology
  • Biochemistry

Background:

  • Antioxidant-rich diets are crucial for mammalian central nervous system function.
  • The impact of berberine (BER) on cerebrocerebellar function in prepubertal rats remains uninvestigated.

Purpose of the Study:

  • To investigate the effects of BER supplementation on neurochemical and behavioral changes in prepubertal male rats.
  • To assess BER's impact on antioxidant status, oxidative stress, inflammation, and neuronal integrity.

Main Methods:

  • Rats were orally administered varying doses of BER (25-200 mg/kg) from postnatal day 28 to 68.
  • Behavioral assessments included open field, hanging wire, and negative geotaxis tests.
  • Neurochemical analyses measured antioxidant enzyme activities, oxidative/inflammatory markers, and Nissl cell counts.

Main Results:

  • BER improved locomotive and motor behaviors, including increased distance traveled and average speed.
  • BER supplementation elevated antioxidant enzyme activities (SOD, CAT, GPx, GSH) and reduced oxidative/inflammatory markers (RONS, LPO, TNF-α).
  • BER treatment led to fewer dark-stained Nissl cells, indicating reduced neuronal degeneration.

Conclusions:

  • Berberine supplementation demonstrates neuroprotective effects in prepubertal rats.
  • BER enhances cerebrocerebellar function by improving behavior, boosting antioxidant defenses, and mitigating oxidative stress and inflammation.
  • These effects may be mediated by the agonistic activity of BER on PPAR-α, PPAR-δ, and PPAR-γ.

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