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Hypoglycaemic Potentials of Frog oil in Alloxan-Induced Diabetic Rats

Received: 4 June 2014    Accepted: 20 June 2014    Published: 30 June 2014
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Abstract

The hypoglycaemic potentials of frog oil in alloxan-induced diabetic rats were investigated. Thirty six male albino rats weighing 120.47±2.52 g was completely randomized into six groups (A-F) comprising 6 animals each. Animals in group A (control) were administered 1 ml of distilled water while those in groups B, C, D, E and F were induced with diabetes mellitus by intraperitoneal administration of alloxan monohydrate (180mg/kg body weight) and in addition were respectively administered distilled water, metformin (a reference antidiabetic drug), 3, 6 and 9 mg/kg body weight of frog oil once daily. Treatment with the oil lasted for 14 days during which blood glucose level and selected biochemical parameters were determined. The results showed that there was significant (p<0.05) reduction in glucose levels in the group treated with 9.0 mg/kg body weight of the oil from 221.22±0.15 to 100.15±0.07 mg/dl, indicating the best antidiabetic activity of all the treatment groups. The oil also caused significant (p<0.05) decrease in serum total bilirubin levels from 8.73±0.07 µmol/L to 2.43±0.03 µmol/L; serum total cholesterol levels from 313.48±0.05 mmol/L to 232.40±0.19 mmol/L; liver aspartate aminotransferase (AST) activity from 76.93±0.02 U/L to 35.25±0.02 U/L; liver alanine aminotransferase (ALT) activity from 85.52±0.05 U/L to 39.71±0.08 U/L respectively. Overall, these findings established the fact that frog oil has hypoglycaemic potentials and thus can be recommended for use in the treatment of diabetes. The results from biochemical parameters indicated that frog oil could also be explored in the control of some of the metabolic dysfunctions normally associated with diabetes.

Published in American Journal of BioScience (Volume 2, Issue 4)
DOI 10.11648/j.ajbio.20140204.12
Page(s) 115-121
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Hypoglycaemic Potentials, Frog Oil, Alloxan, Diabetes Mellitus, Metformin, Blood Glucose

References
[1] Allan CD, and Peter JGD, Enzymic Assay of Total Choles-terol Involving Chemical or Enzymic Hydrolysis. A Com-parison of Methods. Clin. Chem. 1979; 25/6, 976-984.
[2] Baranano SM, Balady GJ, and Criqui MH, "Primary prevention of coronary heart disease: guidance from Framingham: a statement for healthcare professionals from the AHA Task Force on Risk Reduction. American Heart Association". Circulation. 2002; 97 (18): 1876–87.
[3] Bay NV, Study of production and utilization of Earth-norms (periony x excavates) as feed supplement in chicken production systems at farmers’ level. Naong Thang Village, Vientiane, 2002; Pp. 160.
[4] Bosman RJ, Rachel PB, and Anthony F, Tra-jectory analysis of serum biomarker concentration faci-litates outcome prediction after pediatric traumatic and hypoxemic brain injury. Dev. Neurosci. 2005; 32(5-6):396-405.
[5] Bowman WC, and Rand MI, Textbook of pharmacology (3rd Ed). London: Blackwell Scientific Pub 1985; Pp. 1943-1964.
[6] Cantrill JA, Diabetes Mellitus. In: Walker, R. and I. Edwards (Eds.), Clinipharmacy and Therapeutics. 2nd Edn., Churchill Livingstone, London, 1999; pp: 635-652.
[7] Chapatwala K, Boykin MA, and Rajan-na B, Effects of intraperitoneally injected cadmium on renal and hepatic glycogenic enzymes in the rat. Drug.Chem.Toxicol. 1982; 5:305-317.
[8] Dhanabal SP, Raja MK, Ramanathan M, Suresh B, Hypoglycemic activity of Nymphaca stellata leaves ethnolic extract in alloxan-induced diabetic rats. Fitoterapia 2007; 78. 288-91.
[9] Egwin CE, Halima AM, and Ibrahim HO, Purification of frog oil using animal-bone activated car-bon. International Journal of Emerging Technology and Advanced Engineering. 2013; ISSN 2250-2459. ISO 9001:Vol. 3, Issue 3, March 2013.
[10] European Treaty Series, European Convention for the protection of vertebrate animals used for experimental and other scientific purposes. European Treaty Series, Strasbourg, 2005; ETS-123.
[11] Girard-Mauduit S, The lipid triad, or how to reduce residual cardiovascular risk? Annales d’Endocrinologie, 2010; Volume 71, Issue 2, pg: 89-94.
[12] Granner DK, Mayes PA, Rodwell VW, Harper’s Biochemistry, 24th ed, Connecticut, USA, Ap-pleton and Lange. 1996; 586-587.
[13] Guyton Arthur, and John Hall John, Textbook of Medical Physiology, Saunders, September, 1996; ISBN 978-0-7.
[14] Heinz E, Plant glycolipids: structure, isolation and analysis. in Advances in Lipid Methodology - 3, 1996; pp. 211–332 (ed. W.W. Christie, Faty Press, Dundee).
[15] Hughes D, Croaking for their mates. The Country-side 1981; 1 (16). Pp.101-103.
[16] Hussain MA, and Theise ND, Stem-cell therapy for diabetes mellitus. Lancet 2004; 364:203.
[17] Kameswara RB, Renuka SP, Raja-Sekar MD, Antidiabetic activity of Terminalia pallida fruit in alloxan induced diabetic rats. J Ethnopharmacol 2003; 85: 169 - 172.
[18] King H, Aubert R, and Herman WH, Global burden of diabetes, 1995-2025 prevalence, numerical estimates and projections. Diabetes Care, 1998; 21:1414-1431.
[19] Klip A, Cellular Mechanism of Action of Metformin. Diabetes Care 1990; June; 13(6):696-704.
[20] Lands AM, and William EM, "Di-etary fat and health: the evidence and the politics of prevention: careful use of dietary fats can improve life and prevent disease". Annals of the New York Academy of Sciences (Blackwell) 2005; 1055: 179–192.
[21] Larrea DH, Memorandum and frog survey in Vientiane perfective. Living Acquactic Re-sources Research Centre. 2001; Pp. 241-255.
[22] Lyons TJ, Lipoprotein glycation and its metabolic complications. Diabetes Care. 1992; 41(2):67-73.
[23] Malloy HT, and Evelyn KA, The de-termination of bilirubin with the photoelectric colori-meter. J Biol Chem, 1937; 119: 481-490.
[24] Manjunatha H, and Srinivasan K, Hy-polipidemic and antioxidant potency of heat processed turmeric and red pepper in experimental Rats. Afr. J. Food Sci. 2008; 2:1-6.
[25] Mario Edwardo Santos Cabral, Diogenenes de queiroz Dias, Debora Lima Sales, Olga Paiva Oliveira,Diego Alves Teles, Jaoao Antonio de Araujo Filho, Evaluation of the antimicrobial activities and chemical composition of body fat from Amphibians Leptodactylus macrosternum Miranda-Ribeiro (1926) and Leptodactylus vastus Adolf Lutz (1930) in North Brazil. 2013; Evidence-Based Complementary and Al-ternative Medicine.
[26] Marles RJ, and Farnsworth NR, Antidiabetic plant and their active constituents. Phytomedicine, 1995; 2:137-189.
[27] McCarthy M, and Frognel P, Genetic approaches to the molecular understanding of type 2 diabetes. Am. J. Physiol. Endo-crinol. Metab., 2002; 283: E217-E225.
[28] Mooradian AD, Albert SG, Bern-baum M, Plummer S, The effect of glipizide gastrointes-tinal therapeutic system on islet cell hormonal res-ponses to a meal in NIDDM. Diabetes Care; 1996; 19:883-884 (AN:(96440298).
[29] Murray M, and Pizzorno J, Encyclopedia of Natural Medicine, 2nd edi-tion; Prima Health Publishing, Rockling, U.S.A. 1997; Pp. 401-2.
[30] Ngaha EO, Akanji MA, Madusolumuo MA, Studies on correlation between chloroquine-induced tissue damage and serum changes in rats. Experientia 1989; 45:143.
[31] Okere OS, Okoli BJ, and Adeyemo SO, Hypoglycaemic potential of Python regius fat. Re-search Journal in Engineering and Applied Sciences. ©Emerging Academy Resources. 2013; (ISSN: 2276-8467) 2(3):192-198.
[32] Oldhan RS, Biodiver-sity and Hyperdiversity in Nigerian Amphibians 2000.
[33] Pirone C, and Aebi M, "Intracellular func-tions of N-linked glycans". Science 2009; 291(5512): 2364–69.
[34] Porter JR, and Barrett TG, Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pa-thology of insulin resistance and β cell failure. J Med Gene. 2005; 42: 893-902.
[35] Rotshteyn Y, and Zito SW, Application of modified in vitro screening for iden-tifying herbals possessing sulfonylureas-like activity. Journal of Ethnopharmacology 2004; 93: 337–344.
[36] Sarah W, Gojka R, Anders G, Richard S, and Hilary K, Global prevalence of diabetes. Diabetes Care 2004; 27: 1047-1053.
[37] Shahjahan M, Sabi-tha KE, Mallika J, and Shyamala-Devi CS, Effect of Sola-num trilobatum against carbon tetrachloride induced hepatic damage in albino rats. Indian J. Med. Res., 2004; 120: 194-198.
[38] Steward JE, The effect of peri-odontal treatment on glycemic control in parents with type 2 diabetes mellitus. 2002; Vol. 28 pg: 306-310.
[39] Turner RC, Cull CA, Frighi V, Holman RR, Glycaemic control with diet, sulfonylurea, metformin: Progressive requirements for multiple therapies 2005; 12: 281-312.
[40] Verge CF, Gianani R, and Kawasaki E, Predicting type one diabetes in first degree relatives using a combination of insulin, GAD and ICA512bdc/1A-2 auto antibodies. Diabetes, 1996; 45: 926-933.
[41] WHO (World Health Organisation), Second report of the WHO expert committee on Di-abetes mellitus. World Health Organization, Technical Report Series. 1980; 646, Geneva, pp: 66.
[42] Willis JA, Scott RS, and Brown LJ, Islet cell antibodies and an-tibodies against glutamic acid decarboxylase in newly diagnosed adult onset diabetes mellitus. Diabetes Res. Clin. Pract, 1996; 33: 89-97.
[43] Yamamoto H, Uchigata Y, Okamoto H, Streptozotocin and alloxan in-duce DNA strand breaks and poly (ADP-ribose) synthe-tase in pancreatic islets. Nature 1997; 294. 284-6.
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  • APA Style

    Osheke Shekins Okere, Moses Dele Adams, Uju Dorathy Ejike, Eunice Ogunwole, Ejike Daniel Eze. (2014). Hypoglycaemic Potentials of Frog oil in Alloxan-Induced Diabetic Rats. American Journal of BioScience, 2(4), 115-121. https://doi.org/10.11648/j.ajbio.20140204.12

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    ACS Style

    Osheke Shekins Okere; Moses Dele Adams; Uju Dorathy Ejike; Eunice Ogunwole; Ejike Daniel Eze. Hypoglycaemic Potentials of Frog oil in Alloxan-Induced Diabetic Rats. Am. J. BioScience 2014, 2(4), 115-121. doi: 10.11648/j.ajbio.20140204.12

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    AMA Style

    Osheke Shekins Okere, Moses Dele Adams, Uju Dorathy Ejike, Eunice Ogunwole, Ejike Daniel Eze. Hypoglycaemic Potentials of Frog oil in Alloxan-Induced Diabetic Rats. Am J BioScience. 2014;2(4):115-121. doi: 10.11648/j.ajbio.20140204.12

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  • @article{10.11648/j.ajbio.20140204.12,
      author = {Osheke Shekins Okere and Moses Dele Adams and Uju Dorathy Ejike and Eunice Ogunwole and Ejike Daniel Eze},
      title = {Hypoglycaemic Potentials of Frog oil in Alloxan-Induced Diabetic Rats},
      journal = {American Journal of BioScience},
      volume = {2},
      number = {4},
      pages = {115-121},
      doi = {10.11648/j.ajbio.20140204.12},
      url = {https://doi.org/10.11648/j.ajbio.20140204.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajbio.20140204.12},
      abstract = {The hypoglycaemic potentials of frog oil in alloxan-induced diabetic rats were investigated. Thirty six male albino rats weighing 120.47±2.52 g was completely randomized into six groups (A-F) comprising 6 animals each. Animals in group A (control) were administered 1 ml of distilled water while those in groups B, C, D, E and F were induced with diabetes mellitus by intraperitoneal administration of alloxan monohydrate (180mg/kg body weight) and in addition were respectively administered distilled water, metformin (a reference antidiabetic drug), 3, 6 and 9 mg/kg body weight of frog oil once daily. Treatment with the oil lasted for 14 days during which blood glucose level and selected biochemical parameters were determined. The results showed that there was significant (p<0.05) reduction in glucose levels in the group treated with 9.0 mg/kg body weight of the oil from 221.22±0.15 to 100.15±0.07 mg/dl, indicating the best antidiabetic activity of all the treatment groups. The oil also caused significant (p<0.05) decrease in serum total bilirubin levels from 8.73±0.07 µmol/L to 2.43±0.03 µmol/L; serum total cholesterol levels from 313.48±0.05 mmol/L to 232.40±0.19 mmol/L; liver aspartate aminotransferase (AST) activity from 76.93±0.02 U/L to 35.25±0.02 U/L; liver alanine aminotransferase (ALT) activity from 85.52±0.05 U/L to 39.71±0.08 U/L respectively. Overall, these findings established the fact that frog oil has hypoglycaemic potentials and thus can be recommended for use in the treatment of diabetes. The results from biochemical parameters indicated that frog oil could also be explored in the control of some of the metabolic dysfunctions normally associated with diabetes.},
     year = {2014}
    }
    

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  • TY  - JOUR
    T1  - Hypoglycaemic Potentials of Frog oil in Alloxan-Induced Diabetic Rats
    AU  - Osheke Shekins Okere
    AU  - Moses Dele Adams
    AU  - Uju Dorathy Ejike
    AU  - Eunice Ogunwole
    AU  - Ejike Daniel Eze
    Y1  - 2014/06/30
    PY  - 2014
    N1  - https://doi.org/10.11648/j.ajbio.20140204.12
    DO  - 10.11648/j.ajbio.20140204.12
    T2  - American Journal of BioScience
    JF  - American Journal of BioScience
    JO  - American Journal of BioScience
    SP  - 115
    EP  - 121
    PB  - Science Publishing Group
    SN  - 2330-0167
    UR  - https://doi.org/10.11648/j.ajbio.20140204.12
    AB  - The hypoglycaemic potentials of frog oil in alloxan-induced diabetic rats were investigated. Thirty six male albino rats weighing 120.47±2.52 g was completely randomized into six groups (A-F) comprising 6 animals each. Animals in group A (control) were administered 1 ml of distilled water while those in groups B, C, D, E and F were induced with diabetes mellitus by intraperitoneal administration of alloxan monohydrate (180mg/kg body weight) and in addition were respectively administered distilled water, metformin (a reference antidiabetic drug), 3, 6 and 9 mg/kg body weight of frog oil once daily. Treatment with the oil lasted for 14 days during which blood glucose level and selected biochemical parameters were determined. The results showed that there was significant (p<0.05) reduction in glucose levels in the group treated with 9.0 mg/kg body weight of the oil from 221.22±0.15 to 100.15±0.07 mg/dl, indicating the best antidiabetic activity of all the treatment groups. The oil also caused significant (p<0.05) decrease in serum total bilirubin levels from 8.73±0.07 µmol/L to 2.43±0.03 µmol/L; serum total cholesterol levels from 313.48±0.05 mmol/L to 232.40±0.19 mmol/L; liver aspartate aminotransferase (AST) activity from 76.93±0.02 U/L to 35.25±0.02 U/L; liver alanine aminotransferase (ALT) activity from 85.52±0.05 U/L to 39.71±0.08 U/L respectively. Overall, these findings established the fact that frog oil has hypoglycaemic potentials and thus can be recommended for use in the treatment of diabetes. The results from biochemical parameters indicated that frog oil could also be explored in the control of some of the metabolic dysfunctions normally associated with diabetes.
    VL  - 2
    IS  - 4
    ER  - 

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Author Information
  • Department of Biochemistry, Faculty of Science and Technology, Bingham University, Karu, Nasarawa State, Nigeria

  • Department of Biochemistry, Faculty of Science and Technology, Bingham University, Karu, Nasarawa State, Nigeria

  • Department of Biochemistry, Faculty of Science and Technology, Bingham University, Karu, Nasarawa State, Nigeria

  • Department of Physiology, Faculty of Basic Medical Sciences, Bingham University, Karu, Nasarawa State, Nigeria

  • Department of Physiology, Faculty of Basic Medical Sciences, Bingham University, Karu, Nasarawa State, Nigeria

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