Effect of Glutathione Enriched Polyherbal Formulation on Streptozotocin Induced Diabetic Model by Regulating Oxidative Stress and PKC Pathway
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作者:
Sheethal, S.
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St Thomas Coll, Dept Chem, Kottayam, Kerala, IndiaSt Thomas Coll, Dept Chem, Kottayam, Kerala, India
Sheethal, S.
[1
]
Ratheesh, M.
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St Thomas Coll, Dept Biochem, Kottayam, Kerala, India
St Thomas Coll, Dept Biochem, Kottayam 686574, Kerala, IndiaSt Thomas Coll, Dept Chem, Kottayam, Kerala, India
Ratheesh, M.
[2
,4
]
Jose, Svenia P.
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St Thomas Coll, Dept Biochem, Kottayam, Kerala, IndiaSt Thomas Coll, Dept Chem, Kottayam, Kerala, India
Jose, Svenia P.
[2
]
Sandya, S.
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Indian Inst Sci, Inorgan & Phys Chem, Bangalore, Karnataka, IndiaSt Thomas Coll, Dept Chem, Kottayam, Kerala, India
Sandya, S.
[3
]
机构:
[1] St Thomas Coll, Dept Chem, Kottayam, Kerala, India
[2] St Thomas Coll, Dept Biochem, Kottayam, Kerala, India
[3] Indian Inst Sci, Inorgan & Phys Chem, Bangalore, Karnataka, India
[4] St Thomas Coll, Dept Biochem, Kottayam 686574, Kerala, India
Background: Increasing evidence shows that oxidative stress is one of the root causes of metabolic disorders like diabetes. Glucose oxidation and activation of various metabolic pathways lead to a disproportionate generation of free radicals. This will significantly reduce the antioxidant status in the body. Objectives: In the present study, we aimed to evaluate the effect of a novel glutathione enriched polyherbal formulation on a streptozotocin induced diabetic model. Materials and Methods: Diabetes was induced by a single intraperitoneal injection of streptozotocin. After 3 days of injection, Glibenclamide (5mg/kg), and glutathione enriched polyherbal formulation were given orally for 28 days. Fasting blood glucose and body weight changes were measured at specific intervals. For the study, antioxidant enzymes, lipid peroxidation products, nitrite, liver enzyme markers, gene expression of GLUT-2, and PKC levels were evaluated. Histopathological analysis was also done. Results: The result shows that glutathione enriched polyherbal formulation treated rats significantly reduced their blood glucose and maintained their body weight. As a result, the GLUT-2 expression was reduced, which prevented the activation of PKC. Moreover, oxidative stress was reduced by improving antioxidants like SOD, CAT, GPx, and GSH by inhibiting the lipid peroxidation process. In addition, hepatic damage was also prevented by protecting the liver cells, and thereby shielding the excessive leakage of SGOT, SGPT, and ALP enzymes. The histopathological analysis of the liver gives more support to other data. Conclusion: Findings show that glutathione-enriched polyherbal formulations have a powerful anti-diabetic effect by inhibiting oxidative stress and thus blocking PKC activation.
机构:
Muthayammal Coll Arts & Sci, Ctr Biotechnol, Namakkal 637408, Tamil Nadu, IndiaManonmaniam Sundaranar Univ, Div Ind Toxicol & Pollut Control, Sri Paramakalyani Ctr Environm Sci, Alwarkurichi 627412, Tamil Nadu, India
Banu, G. Sharmila
Kumar, G.
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Manonmaniam Sundaranar Univ, Div Ind Toxicol & Pollut Control, Sri Paramakalyani Ctr Environm Sci, Alwarkurichi 627412, Tamil Nadu, IndiaManonmaniam Sundaranar Univ, Div Ind Toxicol & Pollut Control, Sri Paramakalyani Ctr Environm Sci, Alwarkurichi 627412, Tamil Nadu, India
Kumar, G.
Murugesan, A. G.
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Manonmaniam Sundaranar Univ, Div Ind Toxicol & Pollut Control, Sri Paramakalyani Ctr Environm Sci, Alwarkurichi 627412, Tamil Nadu, IndiaManonmaniam Sundaranar Univ, Div Ind Toxicol & Pollut Control, Sri Paramakalyani Ctr Environm Sci, Alwarkurichi 627412, Tamil Nadu, India
机构:
SRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, IndiaSRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, India
Subhasree, N.
Kamella, Ananthkumar
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SRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, IndiaSRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, India
Kamella, Ananthkumar
Kaliappan, Ilango
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SRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, IndiaSRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, India
Kaliappan, Ilango
Agrawal, Aruna
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Banaras Hindu Univ, Inst Med Sci, Fac Ayurveda, Dept Kriya Sharir, Varanasi 221005, Uttar Pradesh, IndiaSRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, India
Agrawal, Aruna
Dubey, Govind Prasad
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Banaras Hindu Univ, Inst Med Sci, Varanasi 221005, Uttar Pradesh, IndiaSRM Univ, Interdisciplinary Insitute Indian Syst Med, Kancheepuram, Tamil Nadu, India
机构:
Mashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, IranMashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran
Ghorbani, Ahmad
Shafiee-Nick, Reza
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Mashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran
Mashhad Univ Med Sci, Sch Med, Dept Pharmacol, Mashhad 9177948564, IranMashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran
Shafiee-Nick, Reza
Rakhshandeh, Hassan
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Mashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran
Mashhad Univ Med Sci, Sch Med, Dept Pharmacol, Mashhad 9177948564, IranMashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran
Rakhshandeh, Hassan
Borji, Abasalt
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Neyshabur Univ Med Sci, Neyshabur 9318614139, IranMashhad Univ Med Sci, Sch Med, Pharmacol Res Ctr Med Plants, Mashhad 9177948564, Iran