Literatur Review: Hubungan Model Hewan Coba (Faktor Jenis Kelamin dan Hormon) pada Sensitivitas Induksi Streptozotocin sebagai Agen Diabetogenik
Literature Review: The Relationship Model of Test Animal (Factors of Gender and Hormones) on the Sensitivity of the Induction of Streptozotocin as an Agent of Diabetogenic
DOI:
https://doi.org/10.33084/jsm.v7i2.2646Keywords:
Streptozotocin, diabetes melitus, Gender, HormonesAbstract
Diabetes mellitus (DM) is a metabolic disease that global concern and characterized by hyperglycemia. Tests for antidiabetic agents, either discovering new drugs or antidiabetic components, have been developed using experimental animals induced with the diabetogenic agent streptozotocin. The side effects of streptozotocin were reported lower than alloxan. The sensitivity of streptozotocin induction can be relied on by several factors such as sex and hormones—the difference in results in several studies regarding the relationship between streptozotocin induction sensitivity with gender. The research method is a literature review using a systematic approach. Articles are collected through search engines like NCBI, Google Scholar, and ResearchGate by entering keywords. Based on the results of data synthesis on the relationship between streptozotocin induction sensitivity and the sex of the experimental animal, it was found that fifteen articles were related and three articles were not. Sex has a relationship with streptozotocin induction's sensitivity through the hormones estrogen, progesterone, and testosterone.
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References
1. World Health Organization (WHO). 2020. Diabetes melitus. https://www.who.int/health-topics/diabetes#tab=tab_1
2. Setiati S, Alwi I, Sudoyo AW, Simadibrata M, Setiyohadi B, Syam AF. 2017. Buku Ajar Ilmu Penyakit Dalam Jilid II. IV. Jakarta : InternaPublishing; p2325.
3. Husna F, Suyatna FD, Arozal W, Purwaningsih EH. 2019. Model Hewan Coba Pada Penelitian Diabetes. Pharmaceutical Sciences Research. 6(3): 131–41.
4. Deeds MC, Anderson JM, Armstrong AS, Gastineau DA. 2011. Single Dose Streptozotocin Induced Diabetes: Considerations for Study Design in Islet Transplantation Models. Lab Anim. 45(3): p131-140.
5. Aseer KR, Sangwoo WK, Myung-sook C, Yun JW. 2015. Opposite Expression of SPRAC between the Liver and Pancreas in Streptozotocin-Induced Diabetic Rats. Plos One.
6. Guyton AC, Hall JE. 2014. Buku Ajar Fisiologi Kedokteran. Edisi 12. Jakarta : EGC.
7. Choi M, Choi J, Chaudhari H, Aseer K, Mukherjee R, Yun J. 2013. Gender-Dimorphic Regulation of Skeletal Muscle Proteins in Streptozotocin-Induced Diabetic Rats. Cellular Physiology and Biochemistry. 31(2-3): 408-420.
8. Imam K, Sarwar M, Wali U, Siddique L, Perveen S. 2012. Gender and Contractile Functions of Slow and Fast Skeletal Muscles in Streptozotocin Induced Diabetic Sprague Dawley Rats. Romanian Journal of Diabetes Nutrition and Metabolic Diseases. 19(4): 417-424.
9. Takenouchi Y, Kobayashi T, Taguchi K, Matsumoto T, Kamata K. 2010. Gender Differences in Vascular Reactivity of Aortas from Streptozotocin-Induced Diabetic Mice. Biological & Pharmaceutical Bulletin. 33(10): 1692-1697.
10. Aseer K, Yun J. 2013. Gender-dependent expression of pancreatic proteins in streptozotocin-induced diabetic rats. Biotechnology and Bioprocess Engineering. 18(6): 1122-1134.
11. Chaudhari H, Yun J. 2014. Gender-dimorphic regulation of liver proteins in Streptozotocin- induced diabetic rats. Biotechnology and Bioprocess Engineering. 19(1):93-107.
12. Virgen-Ortiz A, Alejandro AI, and Muñiz J. 2018. Gender-effect on the contractile properties of skeletal muscle in streptozotocin-induced diabetic rats. Journal of Musculoskeletal & Neuronal Interactions. 18(2): p255.
13. Chaudhari H, Kim S, Yun J. 2015. Gender‐dimorphic regulation of DJ 1 and its interactions with metabolic proteins in streptozotocin‐induced diabetic rats. Journal of Cellular and Molecular Medicine. 19(5): 996-1009.
14. Park S, Bahk J, Oh A, Gil N, Huh J, Lee J. 2011. Gender difference and change of α1-adrenoceptors in the distal mesenteric arteries of streptozotocin-induced diabetic rats. Korean Journal of Anesthesiology. 61(5): 419.
15. Witcher D, Sakai N, Williams B, Rahimian R, Anderson L. 2010. Gender differences in the effects of streptozotocin-induced diabetes on parasympathetic vasodilatation in the rat submandibular gland. Archives of Oral Biology. 55(10): 745-753.
16. Rebolledo-Solleiro D, Fernández-Guasti A. 2018. Influence of sex and estrous cycle on blood glucose levels, body weight gain, and depressive-like behavior in streptozotocin-induced diabetic rats. Physiology & Behavior. 194: 560-567.
17. Ariza L, Zaguirre M, García M, Blasco E, Rabanal R, Bosch A et al. 2014. Hyperglycemia and hepatic tumors in ICR mice neonatally injected with streptozotocin. Lab Animal. 43(7): 242-249.
18. Aseer K, Kim S, Choi M, Yun J. 2015. Opposite Expression of SPARC between the Liver and Pancreas in Streptozotocin-Induced Diabetic Rats. PLOS ONE. 10(6).
19. Kim B, Kim Y, Nguyen P, Nam H, Suh J. 2020. Sex differences in glucose metabolism of streptozotocin-induced diabetes inbred mice (C57BL/6J). Applied Biological Chemistry. 63(1).
20. Zhang R, Thor D, Han X, Anderson L, Rahimian R. 2012. Sex differences in mesenteric endothelial function of streptozotocin-induced diabetic rats: a
shift in the relative importance of EDRFs. American Journal of Physiology-Heart and Circulatory Physiology. 303(10): p1183-98.
21. Choi JW, Aseer KR, Chaudhari HN, Mukherjee R, Choi M, Yun JW. 2013. Gender dimorphism in regulation of plasma proteins in streptozotocin-induced diabetic rats. Proteomics. 13(16): p2482-94.
22. Íbias J, O'Dell LE, Nazarian A. 2018. Insulin dependent and independent normalization of blood glucose levels reduces the enhanced rewarding effects of nicotine in a rodent model of diabetes. Behav Brain Res. 351:p75-82.
23. Kataoka, M., Kawamuro, Y., Shiraki, N., Miki, R., Sakano, D., Yoshida, T., Yasukawa, T., Kume, K., & Kume, S. 2013. Recovery from diabetes in neonatal mice after a low-dose streptozotocin treatment. Biochemical and biophysical research communications. 430 (3):p1103–08.
24. Kintoko K, Wen Q, Lin X, Zheng N. 2014. Diabetogenic Activity of Streptozotocin on Kunming Strain Mice as Animal Model of Diabetes Mellitus. Pharmacy and Biological Sciences. 9(1):p48-53.
25. Tiano J.P, Mauvais-Jarvis F. 2014. Importance of oestrogen receptors to preserve functional β-cell mass in diabetes. Nat. Rev. Endocrinol. 4: p342-51
26. Morales MP, Marimoto S, Mendoza-Rodriguez CA, Cerbon MA. 2010. The Protective Effect of Testosterone on Streptozotocin-Induced Apoptosis in β-Cells Is Sex Specific. Pancreasjournal. 39(2): p10
2. Setiati S, Alwi I, Sudoyo AW, Simadibrata M, Setiyohadi B, Syam AF. 2017. Buku Ajar Ilmu Penyakit Dalam Jilid II. IV. Jakarta : InternaPublishing; p2325.
3. Husna F, Suyatna FD, Arozal W, Purwaningsih EH. 2019. Model Hewan Coba Pada Penelitian Diabetes. Pharmaceutical Sciences Research. 6(3): 131–41.
4. Deeds MC, Anderson JM, Armstrong AS, Gastineau DA. 2011. Single Dose Streptozotocin Induced Diabetes: Considerations for Study Design in Islet Transplantation Models. Lab Anim. 45(3): p131-140.
5. Aseer KR, Sangwoo WK, Myung-sook C, Yun JW. 2015. Opposite Expression of SPRAC between the Liver and Pancreas in Streptozotocin-Induced Diabetic Rats. Plos One.
6. Guyton AC, Hall JE. 2014. Buku Ajar Fisiologi Kedokteran. Edisi 12. Jakarta : EGC.
7. Choi M, Choi J, Chaudhari H, Aseer K, Mukherjee R, Yun J. 2013. Gender-Dimorphic Regulation of Skeletal Muscle Proteins in Streptozotocin-Induced Diabetic Rats. Cellular Physiology and Biochemistry. 31(2-3): 408-420.
8. Imam K, Sarwar M, Wali U, Siddique L, Perveen S. 2012. Gender and Contractile Functions of Slow and Fast Skeletal Muscles in Streptozotocin Induced Diabetic Sprague Dawley Rats. Romanian Journal of Diabetes Nutrition and Metabolic Diseases. 19(4): 417-424.
9. Takenouchi Y, Kobayashi T, Taguchi K, Matsumoto T, Kamata K. 2010. Gender Differences in Vascular Reactivity of Aortas from Streptozotocin-Induced Diabetic Mice. Biological & Pharmaceutical Bulletin. 33(10): 1692-1697.
10. Aseer K, Yun J. 2013. Gender-dependent expression of pancreatic proteins in streptozotocin-induced diabetic rats. Biotechnology and Bioprocess Engineering. 18(6): 1122-1134.
11. Chaudhari H, Yun J. 2014. Gender-dimorphic regulation of liver proteins in Streptozotocin- induced diabetic rats. Biotechnology and Bioprocess Engineering. 19(1):93-107.
12. Virgen-Ortiz A, Alejandro AI, and Muñiz J. 2018. Gender-effect on the contractile properties of skeletal muscle in streptozotocin-induced diabetic rats. Journal of Musculoskeletal & Neuronal Interactions. 18(2): p255.
13. Chaudhari H, Kim S, Yun J. 2015. Gender‐dimorphic regulation of DJ 1 and its interactions with metabolic proteins in streptozotocin‐induced diabetic rats. Journal of Cellular and Molecular Medicine. 19(5): 996-1009.
14. Park S, Bahk J, Oh A, Gil N, Huh J, Lee J. 2011. Gender difference and change of α1-adrenoceptors in the distal mesenteric arteries of streptozotocin-induced diabetic rats. Korean Journal of Anesthesiology. 61(5): 419.
15. Witcher D, Sakai N, Williams B, Rahimian R, Anderson L. 2010. Gender differences in the effects of streptozotocin-induced diabetes on parasympathetic vasodilatation in the rat submandibular gland. Archives of Oral Biology. 55(10): 745-753.
16. Rebolledo-Solleiro D, Fernández-Guasti A. 2018. Influence of sex and estrous cycle on blood glucose levels, body weight gain, and depressive-like behavior in streptozotocin-induced diabetic rats. Physiology & Behavior. 194: 560-567.
17. Ariza L, Zaguirre M, García M, Blasco E, Rabanal R, Bosch A et al. 2014. Hyperglycemia and hepatic tumors in ICR mice neonatally injected with streptozotocin. Lab Animal. 43(7): 242-249.
18. Aseer K, Kim S, Choi M, Yun J. 2015. Opposite Expression of SPARC between the Liver and Pancreas in Streptozotocin-Induced Diabetic Rats. PLOS ONE. 10(6).
19. Kim B, Kim Y, Nguyen P, Nam H, Suh J. 2020. Sex differences in glucose metabolism of streptozotocin-induced diabetes inbred mice (C57BL/6J). Applied Biological Chemistry. 63(1).
20. Zhang R, Thor D, Han X, Anderson L, Rahimian R. 2012. Sex differences in mesenteric endothelial function of streptozotocin-induced diabetic rats: a
shift in the relative importance of EDRFs. American Journal of Physiology-Heart and Circulatory Physiology. 303(10): p1183-98.
21. Choi JW, Aseer KR, Chaudhari HN, Mukherjee R, Choi M, Yun JW. 2013. Gender dimorphism in regulation of plasma proteins in streptozotocin-induced diabetic rats. Proteomics. 13(16): p2482-94.
22. Íbias J, O'Dell LE, Nazarian A. 2018. Insulin dependent and independent normalization of blood glucose levels reduces the enhanced rewarding effects of nicotine in a rodent model of diabetes. Behav Brain Res. 351:p75-82.
23. Kataoka, M., Kawamuro, Y., Shiraki, N., Miki, R., Sakano, D., Yoshida, T., Yasukawa, T., Kume, K., & Kume, S. 2013. Recovery from diabetes in neonatal mice after a low-dose streptozotocin treatment. Biochemical and biophysical research communications. 430 (3):p1103–08.
24. Kintoko K, Wen Q, Lin X, Zheng N. 2014. Diabetogenic Activity of Streptozotocin on Kunming Strain Mice as Animal Model of Diabetes Mellitus. Pharmacy and Biological Sciences. 9(1):p48-53.
25. Tiano J.P, Mauvais-Jarvis F. 2014. Importance of oestrogen receptors to preserve functional β-cell mass in diabetes. Nat. Rev. Endocrinol. 4: p342-51
26. Morales MP, Marimoto S, Mendoza-Rodriguez CA, Cerbon MA. 2010. The Protective Effect of Testosterone on Streptozotocin-Induced Apoptosis in β-Cells Is Sex Specific. Pancreasjournal. 39(2): p10
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Published
2022-02-01
How to Cite
Pratiwi, E. C., Trinovita, E., & Toemon, A. I. (2022). Literatur Review: Hubungan Model Hewan Coba (Faktor Jenis Kelamin dan Hormon) pada Sensitivitas Induksi Streptozotocin sebagai Agen Diabetogenik: Literature Review: The Relationship Model of Test Animal (Factors of Gender and Hormones) on the Sensitivity of the Induction of Streptozotocin as an Agent of Diabetogenic. Jurnal Surya Medika (JSM), 7(2), 132–141. https://doi.org/10.33084/jsm.v7i2.2646
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