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- Pallavi S. Jamadagni
- Sharad D. Pawar
- Shridhar Chougule
- Manish Wanjari
- Manish Gautam
- Sudesh Gaidhani
- Arun Gurav
- N. Shrikanth
- Dipsundar Sahu
- Manajit Bora
- A. K. Dixit
- Manosi Das
- Narasimhaji Cheemalapati
- Barnail Sinha
- Qadir Alam
- Sharad Pawar
- P. V.Vara Prasad
- Sudesh N. Gaidhani
- Srikanth Ala
- Viswanth Reddy
- Y. R. Sanjaya Kumar
- Thamizh Selvam
- K. K. Ajeesh Kumar
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Jamadagni, Shrirang
- Amelioration of Streptozotocin Induced Cytotoxicity by Mimosa pudica Root Extract - A Proteomic Based In-Vitro Study
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PDF Views:0
Authors
Pallavi S. Jamadagni
1,
Sharad D. Pawar
1,
Shrirang Jamadagni
1,
Shridhar Chougule
1,
Manish Wanjari
1,
Manish Gautam
2,
Sudesh Gaidhani
3,
Arun Gurav
1,
N. Shrikanth
3
Affiliations
1 Regional Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Gandhi Bhavan Road, Kothrud, Pune - 411038, Maharashtra, IN
2 Assam Down Town University, Panikhaiti, Guwahati - 781026, Assam, IN
3 Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, 61-65, Institutional Area, Opposite Janakpuri D Block, New Delhi - 110058, IN
1 Regional Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Gandhi Bhavan Road, Kothrud, Pune - 411038, Maharashtra, IN
2 Assam Down Town University, Panikhaiti, Guwahati - 781026, Assam, IN
3 Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, 61-65, Institutional Area, Opposite Janakpuri D Block, New Delhi - 110058, IN
Source
Toxicology International (Formerly Indian Journal of Toxicology), Vol 29, No 4 (2022), Pagination: 447-454Abstract
The in-vitrocytotoxicity was studied in a pancreatic cell line (RIN5F) using streptozotocin-induced cellular damage. The Cytotoxic dose of aqueous and hydro-alcoholic extracts of Mimosa pudica root powder before and after streptozotocin treatment was studied and protein expression was explored. Both the extracts were subjected to metabolite analysis by LCMS. Mimosa pudica root powder extracts prevented Streptozotocin-induced cellular damage. Proteomics studies indicated both aqueous and hydro-alcoholic extracts of Mimosa pudica regulate proteins related to insulin secretion, glucose uptake, and insulin resistance with marked changes in proteins involved in insulin secretion. The study first time reports cytotoxicity of Mimosa pudica in RIN5F cells and explores protein expression after Mimosa pudica treatment. It was also observed that the abundance of Mimosine is more in Hydro-alcoholic extracts as compared to aqueous extracts.Keywords
LC-MS, Mimosa pudica, Proteomics, RIN5F.References
- Ahuchaogu AA, Chukwu OJ, Echeme JO. Secondary metabolites from Mimosa Pudica: Isolation, purification and NMR characterization. IOSR Journal of Applied Chemistry. 2017; 10(3):15–20. https://doi:10.9790/5736-1003011520
- Ahmad H, Sehgal S, Mishra A, Gupta R. Mimosa pudica L. (Laajvanti): An overview. Pharmacognosy Reviews. 2012; 6(12):115–24. PMid: 23055637 PMCid: PMC3459453, https://doi.org/10.4103/0973-7847.99945
- Kokane DD, More RY, Kale MB, Nehete MN, Mehendale PC GC. Evaluation of wound healing activity of root of Mimosa pudica. J Ethnopharmacol. 2009; 124(2)8:311–5. PMid: 19397984. https://doi:10.1016/j.jep.2009.04.038
- Sahu PR, Khalkho AS, Kumari S, Alam S. Studies on ethnomedicinal uses and formulation of herbal drugs from medicinal plants of Ranchi District - A survey. American Journal of Ethnomedicine [Internet]. 2015; 2(5):284–96. www.ajethno.comhttp://www.ajethno.com
- Sunday RM, Obuotor EM, Kumar A. Antioxidant and antidiabetic properties of Mimosa pudica seeds in Streptozotocin-induced diabetic Wistar rats. Asian Journal of Biotechnology. 2019; 12(1):1–8. https://doi.org/10.3923/ajbkr.2020.1.8
- Gupta R, Vairale MG, Deshmukh RR, Chaudhary PR, Wate SR. Ethnomedicinal uses of some plants used by Gond tribe of Bhandara district, Maharashtra. Indian Journal of Traditional Knowledge. 2010; 9(4):713–7. http://nopr.niscair.res.in/handle/123456789/10324
- Joseph B, George J, Mohan J. Review article pharmacology and traditional uses of Mimosa pudica. International Journal of Pharmaceutical Sciences and Drug Research. 2013; 5(2):41–4. https://ijpsdr.com/index.php/ijpsdr/article/view/239.
- Muhammad G, Hussain MA, Jantan I, Bukhari SNA. Mimosa pudica L., a high-value medicinal plant as a source of bioactives for pharmaceuticals. comprehensive reviews in Food Science and Food Safety. 2016; 15(2):303–15. PMid: 33371596. https://doi.org/10.1111/1541-4337.12184
- Kaur P, Kumar N, Shivananda TN, Kaur G. Phytochemical screening and antimicrobial activity of the plant extracts of Mimosa pudica L. against selected microbes. Journal of Medicinal Plant Research. 2011; 5(22):5356–9. https://opensiuc.lib.siu.edu/ebl/vol2009/iss5/8
- Chitra G, Athira KA, Anitha CT. Phytochemical screening and antibacterial activity of Mimosa pudica L. and Mimosa invisa L. against selected microbes. Nature Environment and Pollution Technology. 2012; 11(3):431-3. https://neptjournal.com/upload-images/NL-39-15-(15)B-1874
- Anonymous. The Ayurvedic Formulary of India. In: The Ayurvedic Formulary of India. 2003. p. 1–110.
- Ministry for Health and Family Welfare. The Ayurvedic Pharmacopoeia of India. Vol. 2, The Ayurvedic Pharmacopoeia of India. 2010. 171 p. http://www.ayurveda.hu/api/API-Vol-2
- Banik G, Bawari M, Choudhury MD, Choudhury S, Sharma GD. Some anti-diabetic plants of Southern Assam. Assam University Journal of Science and Technology. 2010; 5(1):114–9. https://indiabiodiversity.org/biodiv/content/documents/document-ab21e2b6-05f4-47c0-9053-5b0abfcacb69/151
- Adinortey MB, Agbeko R, Boison D, Ekloh W, Kuatsienu LE, Biney EE, Affum OO, Kwarteng J, Nyarko AK. Phytomedicines used for Diabetes Mellitus in Ghana: A systematic search and review of preclinical and clinical evidence. Evidence-based Complementary and Alternative Medicine. 2019; 2019. PMid:31118963 PMCid: PMC6500637. https://doi.org/10.1155/2019/6021209
- Sutar NG, Sutar UN, Behera BC. Antidiabetic activity of the leaves of Mimosa pudica Linn. in albino rats. Journal of Herbal Medicine and Toxicology [Internet]. 2009; 3(1):123–6. https://www.researchgate.net/publication/268438284
- Azwanida. A review on the extraction methods use in medicinal plants, principle, strength and limitation. Medicinal and Aromatic Plants. 2015; 04(03):3–8. https://doi.org/10.4172/2167-0412.1000196
- Promega. Trypsin Gold, Trypsin Gold, Mass Spectrometry Grade, Instruction for Use of Product. 2015; 1–8. Available from: www.promega.com
- Bateman A, Martin MJ, Orchard S, Magrane M, Agivetova R, Ahmad S, Alpi E, Bowler-Barnett EH, Britto R, Bursteinas B B-A-JH. UniProt: The universal protein knowledge base in 2021. Nucleic Acids Research. 2020; 49(8):D480–9. PMid: 33237286 PMCid: PMC7778908. https://doi.org/10.1093/nar/gkaa1100
- Oliveros JC. VENNY. An interactive tool for comparing lists with Venn Diagrams. 2007. https://bioinfogp.cnb.csic.es/tools/venny/index.html
- Wu J, Yan LJ. Streptozotocin-induced type 1 diabetes in rodents as a model for studying mitochondrial mechanisms of diabetic β cell glucotoxicity. Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy. 2015; 8:181–8. PMid: 25897251 PMCid: PMC4396517. https://doi.org/10.2147/DMSO.S82272
- Mardilovich K, Pankratz SL, Shaw LM. Expression and function of the insulin receptor substrate proteins in cancer. Cell Communication and Signaling. 2009; 7:1–15. PMid: 19534786 PMCid: PMC2709114. https://doi. org/10.1186/1478-811X-7-14
- Sun XJ, Rothenberg P, Kahn CR, Backer JM, Araki E, Wilden PA, Cahill DA, Goldstein BJ, White MF. Structure of the insulin receptor substrate IRS-1 defines a unique signal transduction protein. Nature. 1991; 352(6330):73–7. PMid: 1648180. https://doi:10.1038/352073a0
- Pelicci G, Lanfrancone L, Grignani F, McGlade J, Cavallo F, Forni G, Nicoletti I, Grignani F, Pawson T, Pelicci PG. A novel transforming protein (SHC) with an SH2 domain is implicated in mitogenic signal transduction. Cell. 1992; 70(1):93–104. PMid: 1623525. https://doi.org/10.1016/0092-8674(92)90536-L
- Zhou QL, Jiang ZY, Mabardy AS, Del Campo CM, Lambright DG, Holik J, Fogarty KE, Straubhaar J, Nicoloro S, Chawla A, Czech MP. A novel pleckstrin homology domain-containing protein enhances insulin-stimulated Akt phosphorylation and GLUT4 translocation in adipocytes. Journal of Biological Chemistry. 2010; 285(36):27581–9. PMid: 20587420 PMCid: PMC2934625. https://doi.org/10.1074/jbc.M110.146886
- Konstantinova I, Nikolova G, Ohara-Imaizumi M, Meda P, Kučera T, Zarbalis K, Wurst W, Nagamatsu S, Lammert E. EphA-Ephrin-A-mediated beta cell communication regulates insulin secretion from pancreatic islets. Cell. 2007; 129(2):359–70. PMid: 17448994. https://doi.org/10.1016/j.cell.2007.02.044
- Evaluation of Safety and Efficacy of an Ayurvedic Ointment Against Acute Burn Injury in Wistar Rats
Abstract Views :100 |
PDF Views:0
Authors
Dipsundar Sahu
1,
Manajit Bora
1,
A. K. Dixit
1,
Shrirang Jamadagni
2,
Manosi Das
1,
Narasimhaji Cheemalapati
,
Barnail Sinha
,
Qadir Alam
1,
Sharad Pawar
1,
P. V.Vara Prasad
1
Affiliations
1 Central Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Govt. of India, Bidhannagar, Kolkata, West Bengal 700091., IN
2 Regional Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Govt. of India, Kothrud, Pune, Maharashtra 411038., IN
1 Central Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Govt. of India, Bidhannagar, Kolkata, West Bengal 700091., IN
2 Regional Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences, Ministry of AYUSH, Govt. of India, Kothrud, Pune, Maharashtra 411038., IN
Source
Research Journal of Pharmacy and Technology, Vol 15, No 3 (2022), Pagination: 1201-1210Abstract
Skin burn is a common health problem that needs a fast and accurate treatment; else, it can have a worse prognosis. The available treatment options pose limitations due to their adverse effects; thus there is an urgent need to find newer treatment options for burn wound healing that can provide a safer and faster treatment option. Ayurveda gives a plethora of medicinal plants and their formulations which have been used in the management of burn wound. The Ayurvedic ointment formulated in this experiment utilizes essential ayurvedic ingredients which are known for their burn wound healing potential. The current work includes the formulation of the Ayurvedic ointment, its standardization, toxicity and efficacy study. The Ayurvedic ointment was formulated by fusion method, and its physicochemical characterization ensures the purity of the compounds used for the formulation. The ointment formulated is well set under the safety parameters for the presence of heavy metals and also free from microbial and fungal contamination. It has obtained optimum spreadability and viscosity, making it desirable for application on wounds. In the acute dermal toxicity study, it has shown no adverse effect on the animals as there were no significant changes in the body weight and feed intake and water consumption, thus confirming it as a safe formulation. It has shown significant rate of wound healing and period of re-epithelization in the Wistar rat model. It can be a potential ointment for burn wound treatment, and in future, it can be considered for clinical studies to validate its safety and efficacy in humans.Keywords
Burn wound, Ayurveda, Ointment, Fusion method, Re-epithelization.References
- Weaver Jr AJ, Brandenburg KS, Smith BW, Leung KP. Comparative analysis of the host response in a rat model of deep-partial and full-thickness burn wounds with Pseudomonas aeruginosa Infection. Frontiers in Cellular and Infection Microbiology. 2020; 9:466.
- Amini-Nik S, Yousuf Y, Jeschke MG. Scar management in burn injuries using drug delivery and molecular signaling: current treatments and future directions. Advanced Drug Delivery Reviews. 2018; 123:135-154.
- Kaddoura I, Abu-Sittah G, Ibrahim A, Karamanoukian R, Papazian N. Burn injury: review of pathophysiology and therapeutic modalities in major burns. Annals of burns and Fire Disasters. 2017; 30 (2):95-102.
- Vaghardoost R, Majd SGM, Tebyanian H, Babavalian H, Malaei L, Niazi M, Javdani A. The healing effect of sesame oil, camphor and honey on second degree burn wounds in rat. World Journal of Plastic Surgery. 2018; 7(1):67-71.
- Quan TE, Cowper S, Wu S-P, Bockenstedt LK, Bucala R. Circulating fibrocytes: collagen-secreting cells of the peripheral blood. The International Journal of iochemistry & Cell Biology. 2004; 36(4):598-606.
- Abdullahi A, Amini-Nik S, Jeschke M. Animal models in burn research. Cellular and Molecular Life Sciences. 2014; 71 (17):3241-3255.
- Chang S-J, Sartika D, Fan G-Y, Cherng J-H, Wang Y-W. (2019) Animal models of burn wound management. in: Animal Models in Medicine and Biology. 2019. https://www.intechopen.com/chapters/69011.
- Nasiri E, Hosseinimehr SJ, Azadbakht M, Akbari J, Enayati-Fard R, Azizi S, Azadbakht M. The healing effect of Arnebia euchroma ointment versus silver sulfadiazine on burn wounds in rat. World Journal of Plastic surgery. 2015; 4(2):134-144.
- Hosseini SV, Tanideh N, Kohanteb J, Ghodrati Z, Mehrabani D, Yarmohammadi H. Comparison between Alpha and silver sulfadiazine ointments in treatment of Pseudomonas infections in 3rd degree burns. International Journal of Surgery. 2007; 5(1):23-26.
- Bahramsoltani R, Farzaei MH, Rahimi R. Medicinal plants and their natural components as future drugs for the treatment of burn wounds: an integrative review. Archives of Dermatological Research. 2014; 306 (7):601-617.
- Silalahi J, Surbakti C. Burn wound healing activity of hydrolyzed virgin coconut oil. International Journal of PharmaTech Research. 2015; 8 (1):67-73.
- Molee W, Phanumartwiwath A, Kesornpun C, Sureram S, Ngamrojanavanich N, Ingkaninan K, Mahidol C, Ruchirawat S, Kittakoop P. Naphthalene derivatives and quinones from Ventilago denticulata and their nitric oxide radical scavenging, antioxidant, cytotoxic, antibacterial, and phosphodiesterase inhibitory activities. Chemistry & biodiversity, 2018; 15 (3):e1700537. doi: 10.1002/cbdv.201700537.
- Kulac M, Aktas C, Tulubas F, Uygur R, Kanter M, Erboga M, Ceber M, Topcu B, Ozen OA. The effects of topical treatment with curcumin on burn wound healing in rats. Journal of molecular histology. 2013; 44 (1):83-90.
- Khan M, Shahzadi T, Malik S, Shahid M, Ismail M, Zubair M, Iqbal S. Pharmacognostic evaluation of turmeric (Curcuma longa) extracts in diabetic wound healing. The Journal of Animal & Plant Sciences. 2019; 29 (1):68-74.
- Mahboubi M. Rosa damascena as holy ancient herb with novel applications. Journal of Traditional and Complementary Medicine. 2016; 6 (1):10-16.
- Busse D, Kudella P, Grüning N-M, Gisselmann G, Ständer S, Luger T, Jacobsen F, Steinsträßer L, Paus R, Gkogkolou P. A synthetic sandalwood odorant induces wound-healing processes in human keratinocytes via the olfactory receptor OR2AT4. Journal of investigative dermatology. 2014; 134 (11): 2823-2832.
- Palatty P, Azmidah A, Rao S, Jayachander D, Thilakchand K, Rai M, Haniadka R, Simon P, Ravi R, Jimmy R. Topical application of a sandal wood oil and turmeric based cream prevents radiodermatitis in head and neck cancer patients undergoing external beam radiotherapy: a pilot study. The British Journal of Radiology. 2014; 87 (1038): 20130490.
- Temhunna S, Mishra S, Parida N. An Ayurvedic vivechan on arsha vyadhi. International Journal of Health Sciences and Research. 2019; 9 (7):277-281.
- Khan J, Leenoos LM, Ruhi S, Al-Dhalli S, Kaleemullah M, Saad R, Ali HS, Sahu R, Florence M, Rasny M. Development and evaluation of polyherbal halal ointment using honey and Papaya. International Journal of Medical Toxicology & Legal Medicine. 2020; 23 (1-2): 232-238.
- Bora M, Srivastava B, Gaidhani SN, Sharma H, Gautam MK, Tiwari RK, Wanjari MM, Khanduri S, Hazra J. Development of a novel polyherbal formulation for augmenting milk production in healthy dairy cows. Journal of Drug Research in Ayurvedic Sciences. 2019; 4(2): 84-94.
- Gupta S, Raghuwanshi N, Varshney R, Banat IM, Srivastava AK, Pruthi PA, Pruthi V. Accelerated in vivo wound healing evaluation of microbial glycolipid containing ointment as a transdermal substitute. Biomedicine & Pharmacotherapy. 2017; 94:1186-1196.
- Bhatia N, Arunpreet S, Rohit S, Amandeep S, Varinder S, Gurjeet S, Jaideep B, Ravi D, Balwinder S. Evaluation of burn wound healing potential of aqueous extract of Morus alba based cream in rats. Journal of Phytopharmacology. 2014; 3 (6):378-383.
- Liu Y, Xiao X, Ji L, Xie L, Wu S, Liu Z. Camellia cake extracts reduce burn injury through suppressing inflammatory responses and enhancing collagen synthesis. Food & Nutrition Research. 2020; 64: 10.29219/fnr.v64.3782.
- Banchrof J, Steven A, Turner D. Theory and practice of histopathological techniques. Churchil Livingstone, New York, London, San Francisco, Tokyo. 1996.
- Kumar KNS, Holla BS, Ravishankar B, Yashovarma B. Quality standards for Hutabhugadi curṇa (Ayurvedic Formulary of India). Journal of traditional and complementary medicine. 2016, 6 (1):78-88.
- Abraham A, Samuel S, Mathew L. (2018) Phytochemical analysis of Pathyashadangam kwath and its standardization by HPLC and HPTLC. Journal of Ayurveda and Integrative Medicine. 2020; 11(2): 153-158.
- Pahl P. Growth curves for body weight of the laboratory rat. Australian journal of biological sciences. 1969; 22 (4):1077-1080.
- Shahzad MN, Ahmed N. Effectiveness of Aloe vera gel compared with 1% silver sulphadiazine cream as burn wound dressing in second degree burns. Journal of Pakistan Medical Association. 2013; 63 (2):225-230.
- Alemdaroglu C, Degim Z, Çelebi N, Zor F, Ozturk S, Erdogan D. An investigation on burn wound healing in rats with chitosan gel formulation containing epidermal growth factor. Burns. 2006; 32 (3): 319-327.
- Antidiabetic Activity of Vasant Kusumakar Ras in Streptozotocin and High Fat Diet Induced Type 2 Diabetes Mellitus in Sprague Dawley Rats
Abstract Views :157 |
PDF Views:81
Authors
Sudesh N. Gaidhani
1,
Srikanth Ala
1,
Viswanth Reddy
1,
Y. R. Sanjaya Kumar
1,
Shrirang Jamadagni
1,
Thamizh Selvam
1,
K. K. Ajeesh Kumar
1
Affiliations
1 Pharmacology, National Ayurveda Research Institute for Panchakarma, Cheruthuruthy, Thrissur - 679531, Kerala, IN
1 Pharmacology, National Ayurveda Research Institute for Panchakarma, Cheruthuruthy, Thrissur - 679531, Kerala, IN
Source
Journal of Natural Remedies, Vol 23, No 2 (2023), Pagination: 521-536Abstract
Background: VasantKusumakar Ras (VK Ras) is a traditional Ayurvedic preparation used in the treatment of Type-2 diabetes mellitus. Despite its clinical anti-diabetic claims, no pre-clinical attempts were made to rule out its efficacy as an antidiabetic agent. Objectives: The present study was carried out to find the anti-diabetic effect of VK Ras against a High-Fat Diet (HFD), and low-dose streptozotocin (STZ) induced type 2 diabetes and to explore the mode of action of VK Ras. Materials and Methods: Different doses of VK Ras were administered to diabetic rats for 35 days. The biochemical markers analysis, intestinal glucose uptake, and liver glycogen content were estimated at the end of the study and also vital organs were weighed and subjected to histopathological evaluation. Results: VK Ras treatment reduced blood glucose in a dose-dependent manner. The insulin, HbA1C, HOMA-IR, and lipid profiles were improved in VK Ras-treated animals as compared to diabetic control animals. The relative organ weights were changed in diabetic rats, and treatment with VK Ras corrected the organ weights. Intestinal glucose uptake and liver glycogen content were decreased with treatment. Further, the histopathological analysis of the pancreas and other vital organs had shown that dose-dependent restoration of organ function with VK Ras treatment. Conclusions: VK Ras treatment reduces insulin resistance as well as corrects the lipid, hepatic and renal abnormalities that arise from diabetes, these effects may be mediated by interfering with glucose transport from the gut and insulin release from the β pancreatic cells.Keywords
HbA1C, HFD, HOMA-IR, Insulin, STZ, VK RasReferences
- Oschatz E, Müllner M, Herkner H, Laggner AN. Multiple organ failure and prognosis in adult patients with diabetic ketoacidosis. Wien Klin Wochenschr. 1999; 111(15):590-5. PMID: 10483673.
- Leon BM, Maddox TM. Diabetes and cardiovascular disease: Epidemiology, biological mechanisms, treatment recommendations and future research. World J Diabetes. 2015; 6(13):1246-58. https://doi.org/10.4239/wjd.v6.i13.1246 PMid:26468341 PMCid:PMC4600176
- Chaudhary A, Singh N. Contribution of World Health Organization in the global acceptance of Ayurveda. J Ayurveda Integr Med. 2011; 2(4):179-186. https://doi.org/10.4103/0975-9476.90769 PMid:22253507 PMCid: PMC3255448
- McWhorter LS. Biological complementary therapies: A Focus on botanical products in diabetes. Diabetes Spectrum. 2001; 14:199-208. https://doi.org/10.2337/diaspect.14.4.199
- Saxena A, Vikram NK. Role of selected Indian plants in management of type 2 diabetes: a review. Journal of Alternative and Complementary Medicine. 2004; 10:369-78. https://doi.org/10.1089/107555304323062365 PMid:15165418
- Sarkar PK, Das S, Prajapati PK. Ancient concept of metal pharmacology based on Ayurvedic literature. Anc Sci Life. 2010; 29(4):1-6
- Tamoli SM, Kohli KR, Kaikini AA, Muke SA, Shaikh AA, Sathaye S. Vasant Kusmakar Ras, an ayurvedic herbo-mineral formulation prevents the development of diabetic retinopathy in rats. J Ayurveda Integr Med. 2020; 11(3):270-276. https://doi.org/10.1016/j.jaim.2020.02.002 PMid:32312587 PMCid:PMC7527844
- Winzell MS, Ahren B. The high-fat diet-fed mouse: a model for studying mechanisms and treatment of impaired glucose tolerance and type 2 diabetes. Diabetes. 2004; 53(Suppl. 3):S215-S219. https://doi.org/10.2337/diabetes.53.suppl_3. S215 PMid:15561913
- Kanno A, Asahara SI, Masuda K, Matsuda T, Kimura- Koyanagi M, Seino S, Ogawa W, Kido Y. Compensatory hyperinsulinemia in high-fat diet-induced obese mice is associated with enhanced insulin translation in islets. Biochem Biophys Res Commun. 2015; 458(3):681-686. https://doi.org/10.1016/j.bbrc.2015.02.024 PMid:25686499
- Brøndum E, Nilsson H, Aalkjaer C. Functional abnormalities in isolated arteries from Goto-Kakizaki and streptozotocin- treated diabetic rat models. HormMetab Res. 2005; 37 (Suppl 1):56-60 https://doi.org/10.1055/s-2005-861370 PMid:15918112
- Srinivasan K, Viswanad B, Asrat L, Kaul CL, Ramarao P. Combination of high-fat diet-fed and low-dose streptozotocin- treated rat: A model for type 2 diabetes and pharmacological screening. Pharmacological Research. 2005; 52(4):313-320. https://doi.org/10.1016/j.phrs.2005.05.004 PMid:15979893
- Doluisio JT, Billups NF, Dittert LW, Sugita ET, Swintosky JV. Drug absorption. I. An in-situ rat gut technique yielding realistic absorption rates. J Pharm Sci. 1969; 58(10):1196- 200. https://doi.org/10.1002/jps.2600581006 PMid:5394662
- Van der vies J. Two methods for the determination of glycogen in liver. Biochem J. 1954; 57(3):410-6. https://doi.org/10.1042/bj0570410 PMid: 13181850 PMCid: PMC1269772
- Lenzen S. The mechanisms of alloxan- and streptozotocininduced diabetes. Diabetologia. 2008; 51(2):216-26. https:// doi.org/10.1007/s00125-007-0886-7 PMid:18087688
- Strong JS, Bartholomew BA, Smyth CJ. Immunoresponsiveness of patients with rheumatoid arthritis receiving cyclophosphamide or gold salts. Ann Rheum Dis. 1973; 32(3):233-237. https://doi.org/10.1136/ard.32.3.233 PMid:4715541 PMCid:PMC1006085
- Mandal A, Bhattarai B, Kafle P, Khalid M, Jonnadula SK, Lamicchane J, Kanth R, Gayam V. Elevated liver enzymes in patients with type 2 diabetes mellitus and non-alcoholic fatty liver disease. Cureus. 2018 2018; 10(11). https://doi.org/10.7759/cureus.3626
- Ferrannini E, Lanfranchi A, Rohner-Jeanrenaud F, Manfredini G, Van de Werve G. Influence of longterm diabetes on liver glycogen metabolism in the rat. Metabolism. 1990; 39(10):1082-8. https://doi.org/10.1016/0026-0495(90)90170-H PMid:2145494
- Hussain S, Jamali MC, Habib A, Hussain MS, Akhtar M, Najmi AK. Diabetic kidney disease: An overview of prevalence, risk factors, and biomarkers. Clinical Epidemiology and Global Health. 2021; 9:2-6. https://doi.org/10.1016/j. cegh.2020.05.016
- Harita N, Hayashi T, Sato KK, Nakamura Y, Yoneda T, Endo G, Kambe H. Lower serum creatinine is a new risk factor of type 2 diabetes: The Kansai healthcare study. Diabetes Care. 2009; 32:424-426. https://doi.org/10.2337/dc08-1265 PMid:19074997 PMCid:PMC2646021
- DeFronzo RA, Gunnarsson R, Björkman O, Olsson M, Wahren J. Effects of insulin on peripheral and splanchnic glucose metabolism in noninsulin-dependent (type II) diabetes mellitus. J Clin Invest. 1985; 76:149-155. https://doi. org/10.1172/JCI111938 PMid:3894418 PMCid:PMC423730
- Onuigbo MA, Agbasi N. Diabetic nephropathy and CKD-analysis of individual patient serum creatinine trajectories: A forgotten diagnostic methodology for diabetic CKD prognostication and prediction. J Clin Med. 2015; 4(7):1348-68. https://doi.org/10.3390/jcm4071348 PMid: 26239680 PMCid:PMC4519794
- Ni Z, Guo L, Liu F, Olatunji OJ, Yin M. Allium tuberosum alleviates diabetic nephropathy by supressing hyperglycemia- induced oxidative stress and inflammation in high fat diet/streptozotocin treated rats. Biomed Pharmacother. 2019; 112. https://doi.org/10.1016/j.biopha.2019.108678 PMid:30784905
- Gromova LV, Polozov AS, Kornyushin OV, Grefner NM, Dmitrieva YV, Alekseeva AS, Gruzdkov AA. Glucose absorption in the rat small intestine under experimental Type 2 Diabetes Mellitus. J Evol Biochem Physiol. 2019; 55:155-157. https://doi.org/10.1134/S0022093019020091