The control of hyperglycemia by estriol and progesterone in alloxan induced type I diabetes mellitus mice model through hepatic insulin synthesis

International Journal of Biomedical Science

Volumn 10, Issue 1, 2014, Pages 8-15

  Bhattacharya, Suman ^a,b   Bank, Sarbashri ^a   Maiti, Smarajit ^b   Sinha, Asru K ^a  

^a Sinha Institute of Medical Science and Technology   (India)

^b VIDYASAGAR UNIVERSITY   (India)

Author keywords

Dermcidin isoform 2; Hepatocytes; Menopause; Type 1 diabetes mellitus; Type 1B diabetes mellitus

Indexed keywords

ESTRIOL; GLUCOSE; INSULIN; N(G) NITROARGININE METHYL ESTER; NITRIC OXIDE; PROGESTERONE;

ADULT; ALLOXAN-INDUCED DIABETES MELLITUS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL FREE SYSTEM; CONCENTRATION RESPONSE; CONTROLLED STUDY; ENZYME ACTIVATION; ENZYME INHIBITION; ENZYME LINKED IMMUNOSORBENT ASSAY; GLUCOSE BLOOD LEVEL; HYPERGLYCEMIA; INSULIN BLOOD LEVEL; INSULIN SENSITIVITY; INSULIN SYNTHESIS; LIVER CELL; LIVER HOMOGENATE; MOUSE; NONHUMAN; PANCREAS ISLET BETA CELL; PROTEIN ANALYSIS;

EID: 84897871852     PISSN: 15509702     EISSN: 15552810     Source Type: Journal    
DOI: None     Document Type: Article

References (32)

1. Gan MJ, Albanese-O'Neill A, Haller MJ. Type 1 diabetes: Current concepts in epidemiology, pathophysiology, clinical care, and research. Curr. Probl. Pediatr. Adolesc. Health Care. 2012; 42 (10): 269-291.
2. Wedisinghe L, Perera M. Diabetes and the menopause. Maturitas. 2009; 63 (3): 200-203.
3. Gaspard U, van den Brûle F. Menopause-related risk and hormone therapy in diabetic women. Rev. Med. Liege. 2005; 60 (5-6): 586-589.
4. Maharlouei N, Bellissimo N, Ahmadi SM, et al. Prevalence of metabolic syndrome in pre-and postmenopausal Iranian women. Climacteric. 2012; Nov 16.
5. Hidalgo LA, Chedraui PA, Morocho N, et al. The metabolic syndrome among postmenopausal women in Ecuador. Gynecol. Endocrinol. 2006; 22 (8): 447-454.
6. American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. January 2012; 35 (1).
7. Yoon JW, Jun HS. Autoimmune destruction of pancreatic beta cells. Am. J. Ther. 2005; 12 (6): 580-591.
8. Waldron-Lynch F, Herold KC. Immunomodulatory therapy to preserve pancreatic β-cell function in type1diabetes. Nat. Rev. Drug Discov. 2011; 10 (6): 439-452.
9. Powers AC. Diabetes mellitus. Harrison's principles of internal medicine. Edited by Kasper DL, Fauci AS, Longo DL, Braunwald E, Hauser SL, Jameson JL, 16th ed. New York: McGraw-Hill. 2005; p2152.
10. Ghosh R, Bhattacharya R, Bhattacharya G, et al. The control of stress induced Type I diabetes mellitus in humans through the hepatic synthesis of insulin by the stimulation of nitric oxide production. International Journal of Biomedical Science. 2012; 8 (3): 171-182.
11. Ghosh R, Karmohapatra SK, Bhattacharya M, et al. The appearance of dermcidin isoform 2, a novel platelet aggregating agent in the circulation in acute myocardial infarction that inhibits insulin synthesis and the restoration by acetyl salicylic acid of its effects. J. Thromb. Thrombolysis. 2011; 31 (1): 13-21.
12. Ghosh R, Jana P, Sinha AK. The control of hyperglycemia in alloxan treated diabetic mice through the stimulation of hepatic insulin synthesis due to the production of nitric oxide. Exp. Clin. Endocrinol. Diabetes. 2011; 120 (3): 145-151.
13. Asplund K, Westman S, Hellerstrom C. Glucose stimulation of secretion from the isolated pancrease of foetal and newborn rats. Diabetologia. 1969; 5 (4): 260-262.
14. Grodsky GM. A threshold distribution hypothesis for packet storage of insulin and its mathematical modelling. J. Clin. Invest. 1972; 51 (8): 2047-2059.
15. Ghosh R, Karmohapatra SK, Bhattacharya G, et al. The glucose induced synthesis of insulin in liver. Endocr. 2010; 38: 294-302.
16. Ghosh R, Maji UK, Bhattacharya R, et al. The Role of Dermcidin Isoform 2: A Two-Faceted Atherosclerotic Risk Factor for Coronary Artery Disease and the effect of acetyl salicylic Acid on it. Thrombosis. 2012b; 2012: 987932.
17. Guha M, Biswas J, Tirkey J, et al. Impairment of stimulation by estrogen of insulin-activated nitric oxide synthase in human breast cancer. Int. J. Cancer. 2002; 100 (3): 261-265.
18. Ganguly Bhattacharjee K, Bhattacharyya M, Halder UC, et al. The Role of Neutrophil Estrogen Receptor Status on Maspin Synthesis via Nitric Oxide Production in Human Breast Cancer. J. Breast Cancer. 2012a; 15 (2): 181-188.
19. Wahli W, Martinez E. Superfamily of steroid nuclear receptors: positive and negative regulators of gene expression. FASEB J. 1991; 5 (9): 2243-2249.
20. Ganguly Bhattacharjee K, Bhattacharyya M, Halder UC, et al. Effect of progesterone receptor status on maspin synthesis via nitric oxide production in neutrophils in human breast cancer. Breast Cancer. 2012b; DOI 10.1007/s12282-012-0422-6.
21. Lenzen S. The mechanisms of alloxan and streptozotocin-induced diabetes. Diabetologia. 2008; 51 (2): 216-226.
22. Bennett RA, Pegg AE. Alkylation of DNA in rat tissues following administration of streptozotocin. Cancer Res. 1981; 41 (7): 2786-2790.
23. Schmezer P, Eckert C, Liegibel UM. Tissue-specific induction of mutations by streptozotocin in vivo. Mutat. Res. 1994; 307 (2): 495-499.
24. Schein PS, Loftus S. Streptozotocin: depression of mouse liver pyridine nucleotides. Cancer Res. 1968; 28 (8): 1501-1506.
25. Guillam MT, Burcelin R, Thorens B. Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes. Proc. Natl. Acad. Sci. USA. 1988; 95 (21): 12317-12321.
26. Karmohapatra KS, Chakraborty K, Khan NN, et al. The role of nitric oxide in aspirin induced thrombolysis in vitro and the purification of aspirin activated nitric oxide synthesis from human blood platelets. Am. J. Hem. 2007; 82: 986-995.
27. Cox RD, Frank CW. Determination of nitrate and nitrite in blood and urine by chemiluminescence. J. Anal. Toxicol. 1982; 6: 148-152.
28. Engvall E, Perlmann P. Enzyme-linked immunosorbent assay, Elisa. 3. Quantitation of specific antibodies by enzyme-labeled anti-immunoglobulin in antigen-coated tubes. J. Immunol. 1972; 109 (1): 129-135.
29. th ed. NJ: Merck Research Laboratories, Whitehouse station. 2001; p3739.
30. Sakuma I, Stuehr DJ, Gross SS, et al. Identification of arginine as a precursor of endothelium-derived relaxing factor. Proc. Natl. Acad. Sci. USA. 1988; 85: 8664-8667.
31. Rathsman B, Rosfors S, Sjöholm A, et al. Early signs of atherosclerosis are associated with insulin resistance in non-obese adolescent and young adults with type 1 diabetes. Cardiovasc Diabetol. 2012 Nov 27; 11: 145. doi: 10.1186/1475-2840-11-145.
32. Garcia-Garcia HM, Costa MA, Serruys PW. Imaging of coronary atherosclerosis: intravascular ultrasound. Eur. Heart J. 2010; 31 (20): 2456-2469.