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Antioxidant and Antithrombotic Activities of Kenaf Seed (Hibiscus cannabinus) Coat Ethanol Extract in Sprague Dawley Rats
Kuvempu Univ, Dept Biochem Jnansahydri, Shivamogga 577451, Karnataka, India..
Tumkur Univ, Dept Studies & Res Biochem, BH Rd, Tumkur 572103, Karnataka, India.;Tumkur Univ, Ctr Biosci & Innovat, BH Rd, Tumkur 572103, Karnataka, India..
Tumkur Univ, Dept Studies & Res Biochem, BH Rd, Tumkur 572103, Karnataka, India.;Tumkur Univ, Ctr Biosci & Innovat, BH Rd, Tumkur 572103, Karnataka, India..
Kuvempu Univ, Dept Biochem Jnansahydri, Shivamogga 577451, Karnataka, India..
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2023 (English)In: Applied Biochemistry and Biotechnology, ISSN 0273-2289, E-ISSN 1559-0291, Vol. 195, no 2, p. 772-800Article in journal (Refereed) Published
Abstract [en]

Oxidative stress has been implicated in deadly lifestyle diseases, and antioxidants from plant sources are the primary option in the treatment regime. Kenaf seeds are the storehouse of potential natural antioxidant phytoconstituents. Perhaps, none of the studies documented the phytoconstituents and their antioxidant potential from Kenaf seed coat so far. Thus, the current study focuses on exploring the protective effect of Kenaf Seed Coat Ethanol Extract (KSCEE) against sodium nitrite and diclofenac-induced oxidative stress in vitro (red blood cell and platelets model) and in vivo (female Sprague Dawely rat's model) along with the antithrombotic activity. The infrared spectrophotometry data showed the heterogeneous functional groups (CH, OH, C = C, C = C-C) and aromatic rings. Reverse phase high-performance liquid chromatography and gas chromatography-mass spectrometry chromatogram of KSCEE also evidenced the presence of several phytochemicals. KSCEE displayed about 76% of DPPH scavenging activity with an IC50 value of 34.94 mu g/ml. KSCEE significantly (***p < 0.001) normalized the stress markers such as lipid peroxidation, protein carbonyl content, superoxide dismutase, and catalase in sodium nitrite and diclofenac-induced oxidative stress in RBC, platelets, liver, kidney, and small intestine, respectively. Furthermore, KSCEE was found to protect the diclofenac-induced tissue destruction of the liver, kidney, and small intestine obtained from seven groups of female Sprague Dawely rats. KSCEE delayed the clotting time of platelet-rich plasma and platelet-poor plasma and activated partial thromboplastin time, suggesting its anticoagulant property. In addition, KSCEE also exhibited antiplatelet activity by inhibiting both adenosine diphosphate and epinephrine-induced platelet aggregation. In conclusion, KSCEE ameliorates the sodium nitrite and diclofenac-induced oxidative stress in red blood cells, platelets, and experimental animals along with antithrombotic properties.

Place, publisher, year, edition, pages
Springer Nature, 2023. Vol. 195, no 2, p. 772-800
Keywords [en]
Antioxidant, Anticoagulant, Antiplatelet, Oxidative stress, Reactive oxygen species
National Category
Biochemistry Molecular Biology Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:uu:diva-497358DOI: 10.1007/s12010-022-04144-8ISI: 000863137400001PubMedID: 36173546OAI: oai:DiVA.org:uu-497358DiVA, id: diva2:1740342
Available from: 2023-03-01 Created: 2023-03-01 Last updated: 2025-02-20Bibliographically approved

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