BackgroundDiabetes mellitus is often associated with neurohistopathological changes, resulting in cognitive deficits. This study aimed to explore the neurohistopathological alterations induced by Theobroma Cacao and Camellia Sinensis extracts in diabetic male Wistar rats.MethodsIn this randomized controlled trial, a total of 64 male Wistar rats aged between 8 and 12 weeks were allocated evenly into eight different groups. The first group, consisting of eight rats, served as the control, receiving only a standard diet with no additional treatment. The second group was treated with 150mg/kg body weight of alloxan to induce a diabetic model. The third group received a metformin treatment at a dose of 100mg/kg body weight. The fourth and fifth groups were administered with Theobroma cacao and Camellia sinensis extracts, respectively, at respective doses of 340 mg/kg and 200 mg/kg body weight. Groups six and seven were diabetic models treated with either Theobroma cacao extract (340 mg/kg) or Camellia sinensis extract (200 mg/kg). The eighth group, another diabetic model, was treated with a combination of both extracts at the same doses. Brain tissues were harvested at the end of an eight-week treatment period for histopathological evaluation. Cresyl violet staining was the method used for histopathological examination of the harvested brain tissues.ResultsHistopathological evaluations revealed normal neuronal structures in the control group. Alloxan-treated rats displayed significant neurodegeneration, including vacuolization and apoptosis. Metformin treatment showed moderate improvements in the neural architecture. Remarkably, Theobroma Cacao and Camellia Sinensis extracts exhibited protective effects against neurodegeneration in both non-diabetic and diabetic rats. Furthermore, a combination of both extracts in diabetic rats led to synergistic improvements in the neural structures, closely approximating normal conditions. One-way Analysis of Variance (ANOVA) revealed significant differences among the groups (F(7,56) = 24.11, p < 0.001). A Tukey post hoc test further indicated significant improvements in Metformin, Theobroma Cacao, and Camellia Sinensis-treated groups compared to the alloxan-induced diabetes model.ConclusionsBoth Theobroma Cacao and Camellia Sinensis extracts unveiled notable promise in countering the neurohistopathological alterations spurred by diabetes in the study. This pioneering observation accentuates the innovative possibility of utilizing these natural extracts as potential therapeutic agents for neural complications in diabetes mellitus. The compelling findings of this study contribute significantly to the existing body of research and emphatically advocate for further exhaustive exploration into the mechanistic actions of Theobroma Cacao and Camellia Sinensis extracts. The understanding gleaned from such in-depth studies could revolutionize the approach to managing and treating neural complications associated with diabetes, thereby enhancing the quality of life for affected individuals.
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Univ Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Univ Nottingham, Sch Biosci, Loughborough LE12 5RD, England
Rivers State Univ, Fac Agr, Dept Anim Sci, Nkpolu Oroworukwo PMB 5080, Port Harcourt 500101, Rivers State, NigeriaUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Fakae, Lenu B.
Zhong, Jizhou
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Kings Coll London, Inst Pharmaceut Sci, London SE1 9NH, EnglandUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Zhong, Jizhou
Chan, Ka Lung Andrew
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Kings Coll London, Inst Pharmaceut Sci, London SE1 9NH, EnglandUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Chan, Ka Lung Andrew
Mekapothula, Subbareddy
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Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, EnglandUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Mekapothula, Subbareddy
Cave, Gareth W. V.
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Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, EnglandUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Cave, Gareth W. V.
Zhu, Xing-Quan
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Shanxi Agr Univ, Coll Vet Med, Taigu 030801, Shanxi, Peoples R ChinaUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Zhu, Xing-Quan
Stevenson, Carl W.
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Univ Nottingham, Sch Biosci, Loughborough LE12 5RD, EnglandUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
Stevenson, Carl W.
Elsheikha, Hany M.
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Univ Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, EnglandUniv Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, England
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King Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi ArabiaKing Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi Arabia
Ajarem, Jamaan S.
Al-Basher, Gadh
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King Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi ArabiaKing Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi Arabia
Al-Basher, Gadh
Allam, Ahmed A.
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King Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi Arabia
Beni Suef Univ, Dept Zool, Fac Sci, Bani Suwayf, EgyptKing Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi Arabia
Allam, Ahmed A.
Mahmoud, Ayman M.
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Beni Suef Univ, Physiol Div, Dept Zool, Fac Sci, Bani Suwayf, EgyptKing Saud Univ, Dept Zool, Fac Sci, Riyadh, Saudi Arabia