# Modulation of Oxidative Stress and Glycemic Control in Diabetic Wistar Rats: The Therapeutic Potential of Theobroma cacao and Camellia sinensis Diets

**Authors:** Edward Indla, KV Rajasekar, Bandarupalli Naveen Kumar, S. Saravana Kumar, Udaya Kumar P, Suresh Babu Sayana

PMC · DOI: 10.7759/cureus.55985 · Cureus · 2024-03-11

## TL;DR

This study shows that diets containing Theobroma cacao and Camellia sinensis can reduce oxidative stress and improve blood sugar control in diabetic rats.

## Contribution

The study demonstrates the therapeutic potential of cacao and green tea diets in managing diabetes through oxidative stress reduction.

## Key findings

- Theobroma cacao and Camellia sinensis diets significantly affected oxidative stress markers in diabetic rats.
- Blood glucose levels varied across treatment groups, with metformin showing the most significant reduction.
- GSH activity was notably higher in diabetic groups receiving dietary interventions.

## Abstract

Background

Diabetes mellitus is a complex metabolic disorder characterized by oxidative stress and impaired glycemic control. This study investigates the therapeutic potential of Theobroma cacao and Camellia sinensis diets in diabetic Wistar rats and assesses their impact on oxidative stress markers and blood glucose levels.

Methods

In this experiment, eight groups of six male Wistar rats (n = 12.5%), aged 8 to 12 weeks, were carefully set up to see how different treatments for diabetes and oxidative stress affected the two conditions. The random selection process was implemented to minimize any potential bias and ensure that the results of the study would be representative of the general population of Wistar rats. The groups were as follows: a nondiabetic control group (NDC) served as the baseline, while diabetes was induced in the alloxan monohydrate group (150 mg/kg). Another group was given the standard drug metformin (M, 100 mg/kg), and two control groups that did not have diabetes were given extracts of Theobroma cacao (TC, 340 mg/kg) and Camellia sinensis (CS, 200 mg/kg). Three groups of diabetic rats were given a mix of these treatments. Theobroma cacao and Camellia sinensis extracts were given at set doses (TC, 340 mg/kg; CS, 200 mg/kg), along with 150 mg/kg of a drug that causes diabetes. Over a 21-day period, oxidative stress parameters such as glutathione (GSH), malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione reductase (GSHrd) levels, and blood glucose were carefully measured to check for signs of oxidative stress and diabetes progression

Results

Considerable differences in GSH levels were noted across the groups, with the highest GSH concentration found in the group treated with the inducing drug, while the lowest GSH levels were observed in the diabetic group that was administered both Theobroma cacao and Camellia sinensis (p < 0.001). MDA levels also varied, with the diabetic group treated with Theobroma cacao having the highest MDA concentration (3.54 ± 0.29 μmol/L) and the nondiabetic control group treated with Camellia sinensis exhibiting the lowest MDA levels (1.66 ± 0.08 μmol/L; p < 0.001). SOD activity was highest in the standard drug group and lowest in the diabetic group treated with Theobroma cacao. GSH activity was notably higher in the diabetic groups that received dietary interventions (p < 0.001). Blood glucose levels showed diverse responses, with the standard drug group experiencing a substantial reduction, while the inducing drug group exhibited a consistent increase.

Conclusion

The study highlights the significant impact of dietary interventions with Theobroma cacao and Camellia sinensis on oxidative stress markers and blood glucose regulation in diabetic Wistar rats. These findings suggest a potential role for these dietary components in mitigating oxidative stress and improving glycemic control in diabetes, although further research is warranted to elucidate the underlying mechanisms and clinical implications.

## Linked entities

- **Chemicals:** alloxan monohydrate (PubChem CID 16723), metformin (PubChem CID 4091), glutathione (GSH) (PubChem CID 124886)
- **Diseases:** diabetes mellitus (MONDO:0005015)

## Full-text entities

- **Genes:** Gsr (glutathione-disulfide reductase) [NCBI Gene 116686]
- **Diseases:** metabolic disorder (MESH:D008659), impaired glycemic control (MESH:D007174), Diabetes mellitus (MESH:D003920)
- **Chemicals:** alloxan (MESH:D000496), Blood glucose (MESH:D001786), GSH (MESH:D005978), metformin (MESH:D008687), MDA (MESH:D008315)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Camellia sinensis (black tea, species) [taxon 4442], Theobroma cacao (cacao, species) [taxon 3641]

## Full text

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC11007453/full.md

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Source: https://tomesphere.com/paper/PMC11007453