Improvement of Hyperglycemia and Sexual Dysfunction in Diabetic Female Rats by an Artificial Endocrine Pancreas Developed from Mouse β Cells
We investigated the effects of a bioartificial endocrine pancreas (Bio-AEP) produced by mouse β cells on sexual dysfunction of streptozotocin (STZ)-induced diabetic female rats. Female rats were administered STZ (60 mg/kg BW, i.v.) at the age of 10 weeks and transplanted with a Bio-AEP including mou...
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Published in | Experimental Animals Vol. 59; no. 4; pp. 515 - 519 |
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Japanese Association for Laboratory Animal Science
2010
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ISSN | 1341-1357 1881-7122 |
DOI | 10.1538/expanim.59.515 |
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Abstract | We investigated the effects of a bioartificial endocrine pancreas (Bio-AEP) produced by mouse β cells on sexual dysfunction of streptozotocin (STZ)-induced diabetic female rats. Female rats were administered STZ (60 mg/kg BW, i.v.) at the age of 10 weeks and transplanted with a Bio-AEP including mouse β cells at the age of 14 weeks (STZ+Bio-AEP group). Lordosis and proceptive sexual behavior of female rats were observed. The results showed that after the Bio-AEP transplant blood glucose recovered from 380–450 mg/dl induced by streptozotocin to 140–230 mg/dl and suppressed lordosis and proceptive behavior also recovered. These results suggest that it is possible to reverse sexual dysfunction by continuous administration of mouse insulin. |
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AbstractList | We investigated the effects of a bioartificial endocrine pancreas (Bio-AEP) produced by mouse beta cells on sexual dysfunction of streptozotocin (STZ)-induced diabetic female rats. Female rats were administered STZ (60 mg/kg BW, i.v.) at the age of 10 weeks and transplanted with a Bio-AEP including mouse beta cells at the age of 14 weeks (STZ+Bio-AEP group). Lordosis and proceptive sexual behavior of female rats were observed. The results showed that after the Bio-AEP transplant blood glucose recovered from 380-450 mg/dl induced by streptozotocin to 140-230 mg/dl and suppressed lordosis and proceptive behavior also recovered. These results suggest that it is possible to reverse sexual dysfunction by continuous administration of mouse insulin. We investigated the effects of a bioartificial endocrine pancreas (Bio-AEP) produced by mouse β cells on sexual dysfunction of streptozotocin (STZ)-induced diabetic female rats. Female rats were administered STZ (60 mg/kg BW, i.v.) at the age of 10 weeks and transplanted with a Bio-AEP including mouse β cells at the age of 14 weeks (STZ+Bio-AEP group). Lordosis and proceptive sexual behavior of female rats were observed. The results showed that after the Bio-AEP transplant blood glucose recovered from 380–450 mg/dl induced by streptozotocin to 140–230 mg/dl and suppressed lordosis and proceptive behavior also recovered. These results suggest that it is possible to reverse sexual dysfunction by continuous administration of mouse insulin. |
Author | FUNGFUAUG, Wirasak KROMKHUN, Pudcharaporn MORITANI, Naoki YOKOSUKA, Makoto NAKADA, Tomoaki SAITO, Toru R. TERADA, Misao HASHIMOTO, Haruo |
Author_xml | – sequence: 1 fullname: TERADA, Misao organization: Nippon Medical School – sequence: 1 fullname: SAITO, Toru R. organization: Nippon Veterinary and Life Science University – sequence: 1 fullname: KROMKHUN, Pudcharaporn organization: Nippon Veterinary and Life Science University – sequence: 1 fullname: FUNGFUAUG, Wirasak organization: Nippon Veterinary and Life Science University – sequence: 1 fullname: HASHIMOTO, Haruo organization: Nippon Veterinary and Life Science University – sequence: 1 fullname: YOKOSUKA, Makoto organization: Nippon Veterinary and Life Science University – sequence: 1 fullname: MORITANI, Naoki organization: Nippon Veterinary and Life Science University – sequence: 1 fullname: NAKADA, Tomoaki organization: Nippon Veterinary and Life Science University |
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Cites_doi | 10.3109/14767050903550899 10.1177/096368979500400309 10.1111/j.1399-5448.2008.00415.x 10.1055/s-0029-1225352 10.1177/096368979800700410 10.1016/S1701-2163(16)32661-5 10.1538/expanim1978.43.4_581 10.1538/expanim.56.149 10.1177/096368979900800409 10.1210/endo-127-1-126 10.2337/diabetes.39.8.942 10.2174/157339909788920893 10.1016/S0022-5347(17)43042-4 10.1210/endo-124-4-1737 10.1038/cr.2009.28 10.1111/j.0954-6820.1979.tb00721.x 10.1016/0963-6897(96)00044-9 10.1056/NEJM200002033420501 10.3109/07853890008998833 10.1292/jvms.66.129 10.1111/j.1442-2042.2008.02214.x |
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References_xml | – reference: 21. Steger, R.W., Amador, A., Lam, E., Rathert, J., Weis, J., and Smith, M.S. 1989. Endocrinology 124: 1737–1743. – reference: 7. Hirotani, S., Eda, R., Kawabata, T., Fuchinoue, S., Teraoka, S., Agishi, T., and Ohgawara, H. 1999. Cell Transplant. 8: 399–404. – reference: 3. Edamura, K., Nasu, K., Iwami, Y., Nishimura, R., Ogawa, H., Sasaki, N., Ohgawara, H. 2004. J. Vet. Med. Sci. 66: 129–135. – reference: 10. Imagawa, A., Hanafusa, T., Miyagawa, J., and Matsuzawa, Y. 2000. Ann. Med. 32: 539–543. – reference: 5. Hashimoto, H., Arai, T., Ohnishi, Y., Eto, T., Ito, M., Hioki, K., Suzuki, R., Yamauchi, T., Ohsugi, M., Saito, M., Ueyama, Y., Tobe, K., Kadowaki, T., Tamaoki, N., and Kosaka, K. 2007. Exp. Anim. 56: 149–154. – reference: 11. Jensen, S.B., Hagen, C., Frøland, A., and Pedersen, P.B. 1979. Acta Med. Scand. Suppl. 624: 65–68. – reference: 9. Imagawa, A., Hanafusa, T., Miyagawa, J., and Matsuzawa, Y. 2000. N. Engl. J. Med. 342: 301–307. – reference: 14. Miyazaki, J.I., Araki, K., Yamamoto, E., Ikegami, H., Asano, T., Shibasaki, Y., Oka, Y., and Yamamura, K. 1990. Endocrinology 127: 126–132. – reference: 17. Pirkola, J., Vääräsmäki, M., Leinonen, E., Bloigu, A., Veijola, R., Tossavainen, P., Knip, M., and Tapanainen, P. 2008. Pediatr. Diabetes 9: 583–589. – reference: 18. Saito, T.R., Serizawa, I., Hokao, R., Tohei, A., Aoki-Komori, S., Takahashi, K.W. 1994. Exp. Anim. 43: 581–584. – reference: 22. Steger, R.W. and Kienast, S.G. 1990. Diabetes 39: 942–948. – reference: 23. Yonezawa, A., Ebiko, M., Yoshizumi, M., Ise, S.N., Watanabe, C., Mizoguchi, H., Iwasaki, M., Kimura, Y., and Sakurada, S. 2009. Int. J. Urol. 16: 208–211. – reference: 6. Hashimoto, H., Arai, T., Takeguchi, A., Hioki, K., Ohnishi, Y., Kawai, K., Ito, M., Suzuki, R., Yamauchi, T., Ohsugi, M., Saito, M., Ueyama, Y., Tobe, K., Kadowaki, T., Tamaoki, N., and Kosaka, K. 2006. Comp. Med. 56: 176–187. – reference: 20. Sibai, B.M. and Ross, M.G. 2010. J. Matern. Fetal Neonatal Med. 23: 229–233. – reference: 12. McIntyre, H.D., Thomae, M.K,, Wong, S.F., Idris, N., and Callaway, L.K. 2009. Curr. Diabetes Rev. 5: 190–200 – reference: 13. Mircea, C.N., Lujan, M.E., and Pierson, R.A. 2007. J. Obstet. Gynaecol. Can. 29: 887–902. – reference: 15. Ohgawara, H., Miyazaki, J., Karibe, S., Tashiro, F., Akaike, T., and Hashimoto, Y. 1995. Cell Transplant. 4: 307–313. – reference: 2. Butler, R.N., Rubenstein, A.H., Gracia, A.M., and Zweig, S.C. 1998. Geriatrics 53: 47–50, 53–54. – reference: 4. Hashimoto, H., Arai, T., Mori, A., Kawai, K., Hikishima, K., Ohnishi, Y., Eto, T., Ito, M., Hioki, K., Suzuki, R., Ohsugi, M., Saito, M., Ueyama, Y., Okano, H., Yamauchi, T., Kubota, N., Ueki, K., Tobe, K., Tamaoki, N., Kadowaki, T., and Kosaka, K. 2009. Exp. Clin. Endocrinol. Diabetes 117: 577–586. – reference: 8. Hirotani, S. and Ohgawara, H. 1998. Cell Transplant. 7: 407–410. – reference: 16. Ohgawara, H., Miyazaki, J., Nakagawa, Y., Sato, S., Karibe, S., and Akaike, T. 1996. Cell Transplant. 5: S71–73. – reference: 19. Seethalakshmi, L., Menon, M., and Diamond, D. 1987. J. Urol. 138: 190–194. – reference: 1. Briese, V., Voigt, M., Wisser, J., Borchardt, U., and Straube, S. 2010. Arch. Gynecol. Obstet. (Epub ahead of print). – reference: 24. Zhang, D., Jiang, W., Liu, M., Sui, X., Yin, X., Chen, S., Shi, Y., and Deng, H. 2009. Cell Res. 19: 429–438. – ident: 2 – ident: 20 doi: 10.3109/14767050903550899 – ident: 15 doi: 10.1177/096368979500400309 – ident: 17 doi: 10.1111/j.1399-5448.2008.00415.x – ident: 4 doi: 10.1055/s-0029-1225352 – ident: 1 – ident: 8 doi: 10.1177/096368979800700410 – ident: 13 doi: 10.1016/S1701-2163(16)32661-5 – ident: 18 doi: 10.1538/expanim1978.43.4_581 – ident: 5 doi: 10.1538/expanim.56.149 – ident: 7 doi: 10.1177/096368979900800409 – ident: 14 doi: 10.1210/endo-127-1-126 – ident: 22 doi: 10.2337/diabetes.39.8.942 – ident: 12 doi: 10.2174/157339909788920893 – ident: 19 doi: 10.1016/S0022-5347(17)43042-4 – ident: 21 doi: 10.1210/endo-124-4-1737 – ident: 24 doi: 10.1038/cr.2009.28 – ident: 6 doi: 10.1538/expanim.56.149 – ident: 11 doi: 10.1111/j.0954-6820.1979.tb00721.x – ident: 16 doi: 10.1016/0963-6897(96)00044-9 – ident: 9 doi: 10.1056/NEJM200002033420501 – ident: 10 doi: 10.3109/07853890008998833 – ident: 3 doi: 10.1292/jvms.66.129 – ident: 23 doi: 10.1111/j.1442-2042.2008.02214.x |
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Snippet | We investigated the effects of a bioartificial endocrine pancreas (Bio-AEP) produced by mouse β cells on sexual dysfunction of streptozotocin (STZ)-induced... We investigated the effects of a bioartificial endocrine pancreas (Bio-AEP) produced by mouse beta cells on sexual dysfunction of streptozotocin (STZ)-induced... |
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SubjectTerms | Animals bioartificial endocrine pancreas Diabetes Mellitus, Experimental - physiopathology Diabetes Mellitus, Experimental - surgery diabetic rats Female Hyperglycemia - surgery Insulin-Secreting Cells Islets of Langerhans Transplantation - methods Mice Ovariectomy Pancreas, Artificial Posture Rats Sexual Behavior, Animal - physiology Sexual Dysfunction, Physiological - physiopathology Sexual Dysfunction, Physiological - surgery streptozotocin Transplantation, Heterologous |
Title | Improvement of Hyperglycemia and Sexual Dysfunction in Diabetic Female Rats by an Artificial Endocrine Pancreas Developed from Mouse β Cells |
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