Research ArticlePharmacognosy ResearchVol. 15 | Issue 3 | 2026 | pp. 544–550Open access
Evaluation of Protective Effects of Polyphenols of the Marine Brown Alga Ecklonia cava against Potassium Bromate Induced Nephrotoxicity in Rats
- 1*,
- 2,
- 3,
- 4,
- 5,
- 6
- 1 Department of Pharmacology, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.
- 2 BGS GIMS Research Institute, BGS Global Institute of Medical Sciences, Bengaluru, Karnataka, INDIA.
- 3 Department of Pharmacology, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.
- 4 Department of Pharmaceutics, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.
- 5 Department of Pharmacy, Yeungnam University, Gyeongsangbuk-do, SOUTH KOREA.
- 6 Department of Pharmacology, Karnataka College of Pharmacy, Bangalore, Karnataka, INDIA.
Published in Pharmacognosy Research
Correspondence: Moqbel Ali Moqbel Redhwan
Department of Pharmacology, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.
Email: moqbelali22@gmail.com
Copyright: © 2026 Manuscript Technomedia. This is an open access article.
- Published:
- Aug 14, 2026
- Received:
- Mar 1, 2023
- Accepted:
- May 17, 2023
How to cite
Redhwan, M. A. M., Samaddar, S., MG, H., Hard, S. A. A. A., Deka, G., & Godfrey, A. (2026). Evaluation of Protective Effects of Polyphenols of the Marine Brown Alga Ecklonia cava against Potassium Bromate Induced Nephrotoxicity in Rats. Pharmacognosy Research, 15(3), 544–550. https://doi.org/10.5530/pres.15.3.057
Abstract
Background: Ecklonia cava is a kelp (brown algae) genus belonging to Lessoniaceae with plenty of Eckol-type phlorotannins. It exhibits antioxidant, anti-inflammatory, and antibacterial activity. Objectives: This study investigated Ecklonia cava (EC) polyphenols for their protective effects against KBrO3-induced nephrotoxicity in rats. Materials and Methods: The polyphenolic fraction was isolated from EC. Group, I was control (untreated), and group II was administered KBrO3 (135 mg/kg b.w) intragastric for four weeks. Group III was administered ECPP (200 mg/kg b.w) concurrently with KBrO3 (135 mg/kg b.w) orally, and Group VI was administered Rutin (100 mg/ kg b.w) along with KBrO3 (135 mg/kg b.w) orally. The protective effects of ECPP on KBrO3-induced nephrotoxicity in rats were assessed for the biochemical parameters of serum, various antioxidant enzymes, and histopathological changes in kidneys. Results: The level of serum of Blood Urea Nitrogen (BUN), uric acid, and creatinine was suggestively augmented (p<0.001) when treated by KBrO3. The activity of antioxidant enzymes, superoxide dismutase, catalase, glutathione peroxidase, and FRAP (ferric ion reducing antioxidant parameter) were diminished (p<0.001). At the same time, lipid peroxidation and nitric oxide were raised (p<0.001) with KBrO3 treatment in the kidneys. In addition, the protein carbonyl level was amplified (p<0.001) with KBrO3 administration. Histological studies presented renal damage in KBrO3-treated animals where tissue injury was abridged in ECPP pretreatment groups. Conclusion: These results suggest that ECPP functions as an antioxidant in vivo by scavenging reactive oxygen species, which helps preclude oxidative renal injury in rats treated with KBrO3.
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Article metadata
| Title | Evaluation of Protective Effects of Polyphenols of the Marine Brown Alga Ecklonia cava against Potassium Bromate Induced Nephrotoxicity in Rats |
|---|---|
| Authors | Moqbel Ali Moqbel Redhwan; Suman Samaddar; Hariprasad MG; Sumaia Abdulbari Ahmed Ali Hard; Gitima Deka; Anyembe Godfrey |
| Affiliations | Department of Pharmacology, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.; BGS GIMS Research Institute, BGS Global Institute of Medical Sciences, Bengaluru, Karnataka, INDIA.; Department of Pharmacology, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.; Department of Pharmaceutics, KLE College of Pharmacy, Bangalore, Karnataka, INDIA.; Department of Pharmacy, Yeungnam University, Gyeongsangbuk-do, SOUTH KOREA.; Department of Pharmacology, Karnataka College of Pharmacy, Bangalore, Karnataka, INDIA. |
| Corresponding author | moqbelali22@gmail.com |
| Journal | Pharmacognosy Research |
| Volume / Issue | Vol. 15, Issue 3 (2026) |
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