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Antidiabetic, antidyslipidemia, and renoprotector potency of butterfly pea flower extract ( Clitorea ternatea L.) in diabetes mellitus and dyslipidemia rats model

Diabetes mellitus (DM) is a long-term condition marked by high blood glucose levels caused by insulin resistance which will lead to complications of other diseases such as dyslipidemia, which also affects the health of the liver and kidneys. Butterfly pea flower ( L.) has phenolic and flavonoid comp...

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Published in:Open veterinary journal (Tripoli, Libya) Libya), 2024-05, Vol.14 (5), p.1135-1145
Main Authors: Widowati, Wahyu, Darsono, Lusiana, Natariza, Maria R, Waluyo, Novaldo W, Gleyriena Tenda, Abigail M, Siahaan, Berlian H, Oktaviani, Reza, Zahiroh, Fadhilah Haifa, Utomo, Herry S, Rizal, Rizal
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Language:English
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Summary:Diabetes mellitus (DM) is a long-term condition marked by high blood glucose levels caused by insulin resistance which will lead to complications of other diseases such as dyslipidemia, which also affects the health of the liver and kidneys. Butterfly pea flower ( L.) has phenolic and flavonoid compounds which have the potential as herbal medicines for antidiabetics. The purpose of this study is to examine the potential of butterfly pea flower extract (BPE) as an antidiabetic, anti-dyslipidemia, and renoprotection. test was performed on Sprague Dawley rats ( L.) induced by Streptozotocin-Nicotinamide and High Fat Diet-Propylthiouracil as models of DM and dyslipidemia, and BPE was administered orally (200, 400, and 800 mg/kg BW) for 28 days. glutathione peroxidase (GSH-Px), glutathione S-transferase (GST), tumor necrosis factor-α (TNF-α), nuclear factor-kappa beta (NF-kB), alkaline phosphatase (ALP), liver albumin levels, serum blood urea nitrogen (BUN), serum creatinine, and serum uric acid (UA), were measured by ELISA and colorimetry methods. Treatment of BPE 800 mg/kg BW increased levels of GSH-Px, GST, albumin, and serum protein. BPE decreased TNF-α, NF-kB, and ALP. BPE also decreased BUN, serum CR, and serum UA. BPE has the potential to be used as a drug alternative for the treatment of DM and dyslipidemia as well as a hepatoprotective and renoprotective agent.
ISSN:2218-6050
2226-4485
2218-6050
DOI:10.5455/OVJ.2024.v14.i5.7