Main Article Content
Abstract
The study was conducted to find out the impact of dexamethasone of different doses on tail regeneration in the electric black ghost knifefish Apteronotus albifrons (Linnaeus, 1766) after two weeks of amputation. Fish were distributed into five equal groups; Dexamethasone drug was applied at concentrations of 0, 1, 2, 3 and 4 mg.l-1. Water was exchanging every 48 hours with new prepared drug to ensure its stability in treatments. Concentrations 1, 2 and 3 mg.l-1 were not lethal , while the concentration 4 mg.l-1 was lethal, It was observed that fish were dead after four days for concentration 4 mg.l-1.The study showed that the group of control was increased considerably (P < 0.05) (4.5mm± 0.866) in the tail after 14 days of amputation in comparing with treated groups. Treated groups (1, 2 and 3 mg.l-1) showed slowly increase with an average 2.83mm ±0.763, 2.50mm ±0.500, and 2.33mm ±0.577 respectively. The mean of relative gene expression of the junb was 1.109 in control group that is significant (P < 0.05) compared with treated groups that showed a decrease in junb expression (0.074 for 1 mg.l-1, 0.050 for 2 mg.l-1 and 0.006 for 3 mg.l-1). Current study concludes that dexamethasone inhibit tissues regeneration after amputation via suppress stem cells growth, and junb gene specific for stem cells enhancing and the drug reduced its expression.
Keywords
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
References
- Akimenko, M. A., Mari-Beffa, M., Becerra, J., & Geraudie, J. (2003). Old questions, new tools, and some answers to the mystery of new tools, and some answers to the mystery of fin regeneration. Development Dynamics, 226(2), 190 -201.
- https://doi.org/10.1002/dvdy.10248
- Alshami, I. J. J., Ono, Y., Correia, A., Hacker, C., Lange, A., Scholpp, S., Kawasaki, M., Ingham, P. W., & Kudoh, T. (2020). Development of the electric organ in embryos and larvae of the knifefish, Brachyhypopomus gauderio. Developmental Biology, 466, 99-108.
- https://doi.org/10.1016/j.ydbio.2020.06.010
- Alshami, I. J. J., & Saud, H. A. (2021). Mesoderm signaling pathways of early development in the Zebrafish, Danio rerio (Hamilton, 1822). Egyptian Journal of Aquatic Biology & Fisheries, 25(2), 601-614.
- https://doi.org/10.21608/EJABF.2021.165931
- Bechara, I. J., Joazeiro, P. P., Mari-Beffa, M., Becerra, J., & Montes, G. S. (2000). Collagen-affecting drugs impair regeneration of teleost tail fins. Journal of Submicroscopic Cytology and Pathology, 32(2), 273-280.
- https://pubmed.ncbi.nlm.nih.gov/11085216/
- Bechara, I. J., Böckelmann, P. K., Montes, G. S., & Cruz- Hofling, M. A. (2003). Inhibitio of caudal fin actinotrichia regeneration by acetylsalic ylic acid (aspirin) in teleosts. Brazilian Journal of Morphological Sciences, 20, 6.
- https://pesquisa.bvsalud.org/portal/resource/pt/lil-355086
- Briot, K., & Roux, C. (2015). Glucocorticoid-induced osteoporosis. RMD Open, 1(1).
- https://doi.org/10.1136/rmdopen-2014-000014
- Cea, L. A. , Balboa, E., Puebla, C., Vargas, A. A., Cisterna, B. A., Escamilla, R., Regueira, T., & Sáez, J. C. (2016). Dexamethasone-induced muscular atrophy is mediated by functional expression of connexin-based hemichannels. Biochimica et Biophysica Acta -Molecular Basis of Disease, 1862, 891-1899.
- https://doi.org/10.1016/j.bbadis.2016.07.003
- Chang, J. K., Li , C. J., Liao, H. J., Wang, C. K., Wang, G. J., & Ho, M. L . (2009). Anti- inflammatory drugs suppress proliferation and induce apoptosis through altering expressions of cell cycle regulators and pro-apoptotic factors in cultured human osteoblasts. Toxicology, 258(2-3), 148-156.
- https://doi.org/10.1016/j.tox.2009.01.016
- Christian, S., Jan, F., Thorbjorn, G., Allan, F., Moira, S. L., Robert, C. B., & Hans, O. (1999). Serum free insulin – like growth factor – 1 is dose-dependently decreased by methylprednisolone and related to body weight changes in rats. Growth hormone and IGF Research, 9, 74-80.
- https://doi.org/10.1054/ghir.1999.0090
- Chaichit, S., Sato, T., Yu, H., Tanaka, Y. k., Ogra, Y., Mizoguchi, T., & Itoh, M. (2021). Evaluation of dexamethasone- induced osteoporosis in vivo using zebrafish scales. Pharmaceuticals, 14(6), 536.
- https://doi.org/10.3390/ph14060536
- Coutinho, A. E., & Chapman, K. E. (2011). The anti-inflammatory and immunosuppressive effects of glucocorticoids, recent developments and mechanistic insights. Molecular and Cellular Endocrinology, 335, 2-13.
- https://doi.org/10.1016/j.mce.2010.04.005
- Fleischli, J., & Adams, W. (1999). Use of postoperative steroids to reduce pain and inflammation. Journal of Foot Ankle Surgery, 3232-237.
- https://doi.org/10.1016/S1067-2516(99)80059-3
- Florin, L., J., Knebel, P., Zigrino, B., Vonderstrass, C., Mauch, M., Schorpp-Kistner, A., & Szabowski, P. (2006). Delayed wound healing and epidermal hyperproliferation in mice lacking JunB in the skin. Journal of Investigative Dermatology, 126, 902-911.
- https://doi.org/10.1038/sj.jid.5700123
- Froese, R., & Pauly D. (2005). "Apteronotus albifrons" in Fish Base. May. 2005 version.
- https://www.fishbase.se/summary/apteronotus-albifrons.html
- Gurtner, G. C., Werner, S., Barrandon, Y., & Longaker, M. T. (2008). Wound repair and regeneration. Nature, 453, 314-331.
- https://doi.org/ 10.1038/nature07039
- Hamouda, S. A. & Yasear, Y. (2009). Effect of dexamethasone on osteoclast formation in the alveolar bone of rabbits. Iraqi Journal of Veterinary Sciences, 23(1), 13-16.
- https://doi.org/10.33899/ijvs.2009.5690
- Hassan, B. R. (2016). Impact of clove and mustard as anesthetics on small common carp (Cyprinus carpio L.). M. Sc. Thesis, University of Sulaimani, 125pp.
- Ishida, T., Nakajima, T., Kudo, A., & Kawakami, A. (2010). Phosphorylation of Junb family proteins by the Jun N-terminal kinase supports tissue regeneration in zebrafish. Developmental Biology, 340(2), 468-479.
- https://doi.org/10.1016/j.ydbio.2010.01.036
- Ishido, M., Uda, M., Kasuga, N., & Masuhara, M. (2009). The expression patterns of Pax7 in satellite cells during overload-induced rat adult skeletal muscle hypertrophy. Acta Physiolica, 195, 459-469.
- https://doi.org/10.1111/j.1748-1716.2008.01905.x
- Johnson, S., & Weston, J. (1995). Temperature-sensitive mutations that cause stage-specific defects in zebrafish fin regeneration. Genetics, 141(4), 1583-1595.
- https://doi.org/10.1093/genetics/141.4.1583
- Katagiri, T., Kameda, H., Nakano, H. & Yamazaki, S. (2021). Regulation of T cell differentiation by the AP-1 Transcription Factor Junb. Immunoligical Medecine, 44(3), 1-12.
- https://doi.org/10.1080/25785826.2021.1872838
- Kawakami, A. (2010). Stem cell system in tissue regeneration in fish. Development Growth Differentiation, 52, 77-87.
- https://doi.org/10.1111/j.1440-169X.2009.01138.x
- Kawashima, T., Nakamura, A., Yasuda, K., & Kageyama, Y. (2003). Dmaf, a novel member of Maf transcription factor family is expressed in somatic gonadal cells during embryonic development and gametogenesis in Drosophila. Gene Expression Patterns, 3(5), 663-667.
- https://doi.org/10.1016/s1567-133x(03)00093-0
- Kristin, K., Katrin, B., Laura, G. M., Sandra, J. S., Bettina, H., Peter, A., Jens, K., & Schorpp-Kistner, M. (2015). Junb controls lymphatic vascular development in zebrafish via miR-182. Scientific Reports, 5, 15007.
- https://doi.org/10.1038/srep15007
- Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods, 25, 402–408.
- https://doi.org/10.1006/meth.2001.1262
- Meder, B., Just, S., Vogel, B., Rudloff, J., Gärtner, L., Dahme, T., Inken, H., Zankl, A., Katus, H. A., & Rottbauer, W. (2010). Junb-CBF signaling is essential to maintain sarcomeric Z-disc structure and when defective leads to heart failure. Journal of Cell Science, 123(15), 2613-262.
- https://doi.org/10.1242/jcs.067967
- Murciano, C. Pérez, C. J., Smith, A., Avaron, F., Fernȃndez, T. D., Durȃn I., Ruiz-Sánchez, J., Garcĩa, F., Becerra, J., Akimenko, M. A., & Marĩ –Beefa, M. (2007). Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio. Developmental Biology, 312, 272-283.
- https://doi.org/10.1016/j.ydbio.2007.09.026
- Nakamura, M., Yoshida, H., Takahashi, E., Wlizl, M., Takebayashi-Suzuki KHorb, M. E., & Suzuki, A. (2020). The AP-1 transcription factor junb functions in xenopus tail regeneration by positively regulating cell proliferation. Biochemical Biophysical Research Communications, 522, 990-995.
- https://doi.org/10.1016/j.bbrc.2019.11.060
- Nechiporuk, A., & Keating, M. T. (2002). A proliferation gradient between proximal and msxb-expressing distal blastema directs zebrafish fin regeneration. Development, 129(11), 2607-2617.
- https://doi.org/10.1242/dev.129.11.2607
- Poss, K. D., Shen, J., & Keating, M. T. (2000a). Induction of lef1 during zebrafish fin regeneration. Developmental Dynamics, An official publication of the American Association of Anatomists, 219(2), 282-286.
- https://doi.org/10.1002/1097-0177(2000)9999:9999<::AID-DVDY1045>3.0.CO;2-C
- Poss, K. D., Shen, J., & Nechiporuk, A. (2000b). Roles for Fgf signaling during zebrafish fin regeneration. Developmental Biology, 222(2), 347-358.
- https://doi.org /10.1006/dbio.2000.9722
- Rolland-Lagan, A. G., Paquette, M., Tweedle, V. & Akimenko, M. A. (2012). Morphogen-based simulation model of ray growth and joint patterning during fin development and regeneration. Development, 139, 1188-1197.
- https://doi.org/10.1242/dev.073452
- SAS. (2012). Statistical Analysis System, User's Guide. Statistical, Version 9.1th ed. SAS. Inst. Inc. Cary. N.C.
- Sharif, F., Steenbergen, P. J., Metz, J. R., & Champagne, D. L. (2015). Long-lasting effects of dexamethasone on immune cells and wound healing in the zebrafish. Wound Repair and Regeneration, 23(6), 855-865.
- https://doi.org/10.1111/wrr.12366
- Schorpp-Kistner, M., Z. Q. Wang, P., & Angel, E. F. (1999). JunB is essential for mammalian placentation. The EMBO Journal, 18, 934-948.
- https://doi.org/10.1093/emboj /18.4.934
- Stoick, C. L., Moon, R. T., & Weidinger, G. (2007). Advances in signaling in vertebrate regeneration as a prelude to regenerative medicine. Genes & Development, 21, 1292-1315.
- https://doi.org/10.1101/gad.1540507
- Vegiopoulos, A., & Herzig, S. (2007). Glucocorticoids, metabolism and metabolic diseases. Molecular and Cellular Endocrinology, 275, 43-61.
- https://doi.org/10.1016/j.mce.2007.05.015
- Wang, J., Ho, S., Liu, Y. Lee, S. C., Liu, Y. C., Liao, Y. C., & Ho, C. M. (1999). Dexamethasone reduces nausea and vomiting after laparoscopic cholecystectomy. British Journal of Anaesthesia, 83(5), 772-774.
- https://doi.org/10.1093/bja/83.5.772
- Weber, C. M., Martindale, M. Q., Tapscott, S. J., & Unguez, G. A. (2012). Activation of Pax7-positive cells in a non-contractile tissue contributes to regeneration of myogenic tissues in the electric fish S. macrurus. PLoS One, 7(5).
- https://doi.org/10.1371/journal.pone.0036819
- Yin, V. P., & Poss, K. D. (2008). New regulators of vertebrate appendage regeneration. Current Opinion in Genetics & Development, 18(4), 381-386.
- https://doi.org/10.1016/j.gde.2008.06.008
- Yoshida, H., Okada, M., Takebayashi-Suzuki, K., Ueno, N., & Suzuki, A. (2016). Involvement of JunB proto-oncogene in tail formation during early Xenopus embryogenesis. Zoological Science, 33(3), 282-289.
- https://doi.org/10.2108/zs150136
- Yoshinari, N., Ishida, T., Kudo, A., & Kawakami, A. (2009). Gene expression and functional analysis of zebrafish larval fin fold regeneration. Developmental Biology, 325(1), 71-81.
- https://doi.org/10.1016/j.ydbio.2008.09.028
- Zenz, R., Eferl, R., Kenner, L., Florin, L., Hummerich, L., Mehic, D., Scheuch, H., Angel, P. E., Tschachler, E., & Wagner, E. F. (2005). Psoriasis-like skin disease and arthritis caused by inducible epidermal deletion of Jun proteins. Nature, 437, 369-375.
- https://doi.org/10.1038/nature03963
- Zenz, R., Eferl, R., Scheinecker, C., Redlich, K., Smolen, J., Schonthaler, H. B, Kenner, L., Tschachler, E., & Wagner, E. F. (2008). Activator protein 1 (Fos/Jun) functions in inflammatory bone and skin disease. Arthritis Research & Therapy, 10, 201.
- https://doi.org/10.1186/ar2338
References
Akimenko, M. A., Mari-Beffa, M., Becerra, J., & Geraudie, J. (2003). Old questions, new tools, and some answers to the mystery of new tools, and some answers to the mystery of fin regeneration. Development Dynamics, 226(2), 190 -201.
https://doi.org/10.1002/dvdy.10248
Alshami, I. J. J., Ono, Y., Correia, A., Hacker, C., Lange, A., Scholpp, S., Kawasaki, M., Ingham, P. W., & Kudoh, T. (2020). Development of the electric organ in embryos and larvae of the knifefish, Brachyhypopomus gauderio. Developmental Biology, 466, 99-108.
https://doi.org/10.1016/j.ydbio.2020.06.010
Alshami, I. J. J., & Saud, H. A. (2021). Mesoderm signaling pathways of early development in the Zebrafish, Danio rerio (Hamilton, 1822). Egyptian Journal of Aquatic Biology & Fisheries, 25(2), 601-614.
https://doi.org/10.21608/EJABF.2021.165931
Bechara, I. J., Joazeiro, P. P., Mari-Beffa, M., Becerra, J., & Montes, G. S. (2000). Collagen-affecting drugs impair regeneration of teleost tail fins. Journal of Submicroscopic Cytology and Pathology, 32(2), 273-280.
https://pubmed.ncbi.nlm.nih.gov/11085216/
Bechara, I. J., Böckelmann, P. K., Montes, G. S., & Cruz- Hofling, M. A. (2003). Inhibitio of caudal fin actinotrichia regeneration by acetylsalic ylic acid (aspirin) in teleosts. Brazilian Journal of Morphological Sciences, 20, 6.
https://pesquisa.bvsalud.org/portal/resource/pt/lil-355086
Briot, K., & Roux, C. (2015). Glucocorticoid-induced osteoporosis. RMD Open, 1(1).
https://doi.org/10.1136/rmdopen-2014-000014
Cea, L. A. , Balboa, E., Puebla, C., Vargas, A. A., Cisterna, B. A., Escamilla, R., Regueira, T., & Sáez, J. C. (2016). Dexamethasone-induced muscular atrophy is mediated by functional expression of connexin-based hemichannels. Biochimica et Biophysica Acta -Molecular Basis of Disease, 1862, 891-1899.
https://doi.org/10.1016/j.bbadis.2016.07.003
Chang, J. K., Li , C. J., Liao, H. J., Wang, C. K., Wang, G. J., & Ho, M. L . (2009). Anti- inflammatory drugs suppress proliferation and induce apoptosis through altering expressions of cell cycle regulators and pro-apoptotic factors in cultured human osteoblasts. Toxicology, 258(2-3), 148-156.
https://doi.org/10.1016/j.tox.2009.01.016
Christian, S., Jan, F., Thorbjorn, G., Allan, F., Moira, S. L., Robert, C. B., & Hans, O. (1999). Serum free insulin – like growth factor – 1 is dose-dependently decreased by methylprednisolone and related to body weight changes in rats. Growth hormone and IGF Research, 9, 74-80.
https://doi.org/10.1054/ghir.1999.0090
Chaichit, S., Sato, T., Yu, H., Tanaka, Y. k., Ogra, Y., Mizoguchi, T., & Itoh, M. (2021). Evaluation of dexamethasone- induced osteoporosis in vivo using zebrafish scales. Pharmaceuticals, 14(6), 536.
https://doi.org/10.3390/ph14060536
Coutinho, A. E., & Chapman, K. E. (2011). The anti-inflammatory and immunosuppressive effects of glucocorticoids, recent developments and mechanistic insights. Molecular and Cellular Endocrinology, 335, 2-13.
https://doi.org/10.1016/j.mce.2010.04.005
Fleischli, J., & Adams, W. (1999). Use of postoperative steroids to reduce pain and inflammation. Journal of Foot Ankle Surgery, 3232-237.
https://doi.org/10.1016/S1067-2516(99)80059-3
Florin, L., J., Knebel, P., Zigrino, B., Vonderstrass, C., Mauch, M., Schorpp-Kistner, A., & Szabowski, P. (2006). Delayed wound healing and epidermal hyperproliferation in mice lacking JunB in the skin. Journal of Investigative Dermatology, 126, 902-911.
https://doi.org/10.1038/sj.jid.5700123
Froese, R., & Pauly D. (2005). "Apteronotus albifrons" in Fish Base. May. 2005 version.
https://www.fishbase.se/summary/apteronotus-albifrons.html
Gurtner, G. C., Werner, S., Barrandon, Y., & Longaker, M. T. (2008). Wound repair and regeneration. Nature, 453, 314-331.
https://doi.org/ 10.1038/nature07039
Hamouda, S. A. & Yasear, Y. (2009). Effect of dexamethasone on osteoclast formation in the alveolar bone of rabbits. Iraqi Journal of Veterinary Sciences, 23(1), 13-16.
https://doi.org/10.33899/ijvs.2009.5690
Hassan, B. R. (2016). Impact of clove and mustard as anesthetics on small common carp (Cyprinus carpio L.). M. Sc. Thesis, University of Sulaimani, 125pp.
Ishida, T., Nakajima, T., Kudo, A., & Kawakami, A. (2010). Phosphorylation of Junb family proteins by the Jun N-terminal kinase supports tissue regeneration in zebrafish. Developmental Biology, 340(2), 468-479.
https://doi.org/10.1016/j.ydbio.2010.01.036
Ishido, M., Uda, M., Kasuga, N., & Masuhara, M. (2009). The expression patterns of Pax7 in satellite cells during overload-induced rat adult skeletal muscle hypertrophy. Acta Physiolica, 195, 459-469.
https://doi.org/10.1111/j.1748-1716.2008.01905.x
Johnson, S., & Weston, J. (1995). Temperature-sensitive mutations that cause stage-specific defects in zebrafish fin regeneration. Genetics, 141(4), 1583-1595.
https://doi.org/10.1093/genetics/141.4.1583
Katagiri, T., Kameda, H., Nakano, H. & Yamazaki, S. (2021). Regulation of T cell differentiation by the AP-1 Transcription Factor Junb. Immunoligical Medecine, 44(3), 1-12.
https://doi.org/10.1080/25785826.2021.1872838
Kawakami, A. (2010). Stem cell system in tissue regeneration in fish. Development Growth Differentiation, 52, 77-87.
https://doi.org/10.1111/j.1440-169X.2009.01138.x
Kawashima, T., Nakamura, A., Yasuda, K., & Kageyama, Y. (2003). Dmaf, a novel member of Maf transcription factor family is expressed in somatic gonadal cells during embryonic development and gametogenesis in Drosophila. Gene Expression Patterns, 3(5), 663-667.
https://doi.org/10.1016/s1567-133x(03)00093-0
Kristin, K., Katrin, B., Laura, G. M., Sandra, J. S., Bettina, H., Peter, A., Jens, K., & Schorpp-Kistner, M. (2015). Junb controls lymphatic vascular development in zebrafish via miR-182. Scientific Reports, 5, 15007.
https://doi.org/10.1038/srep15007
Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods, 25, 402–408.
https://doi.org/10.1006/meth.2001.1262
Meder, B., Just, S., Vogel, B., Rudloff, J., Gärtner, L., Dahme, T., Inken, H., Zankl, A., Katus, H. A., & Rottbauer, W. (2010). Junb-CBF signaling is essential to maintain sarcomeric Z-disc structure and when defective leads to heart failure. Journal of Cell Science, 123(15), 2613-262.
https://doi.org/10.1242/jcs.067967
Murciano, C. Pérez, C. J., Smith, A., Avaron, F., Fernȃndez, T. D., Durȃn I., Ruiz-Sánchez, J., Garcĩa, F., Becerra, J., Akimenko, M. A., & Marĩ –Beefa, M. (2007). Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio. Developmental Biology, 312, 272-283.
https://doi.org/10.1016/j.ydbio.2007.09.026
Nakamura, M., Yoshida, H., Takahashi, E., Wlizl, M., Takebayashi-Suzuki KHorb, M. E., & Suzuki, A. (2020). The AP-1 transcription factor junb functions in xenopus tail regeneration by positively regulating cell proliferation. Biochemical Biophysical Research Communications, 522, 990-995.
https://doi.org/10.1016/j.bbrc.2019.11.060
Nechiporuk, A., & Keating, M. T. (2002). A proliferation gradient between proximal and msxb-expressing distal blastema directs zebrafish fin regeneration. Development, 129(11), 2607-2617.
https://doi.org/10.1242/dev.129.11.2607
Poss, K. D., Shen, J., & Keating, M. T. (2000a). Induction of lef1 during zebrafish fin regeneration. Developmental Dynamics, An official publication of the American Association of Anatomists, 219(2), 282-286.
https://doi.org/10.1002/1097-0177(2000)9999:9999<::AID-DVDY1045>3.0.CO;2-C
Poss, K. D., Shen, J., & Nechiporuk, A. (2000b). Roles for Fgf signaling during zebrafish fin regeneration. Developmental Biology, 222(2), 347-358.
https://doi.org /10.1006/dbio.2000.9722
Rolland-Lagan, A. G., Paquette, M., Tweedle, V. & Akimenko, M. A. (2012). Morphogen-based simulation model of ray growth and joint patterning during fin development and regeneration. Development, 139, 1188-1197.
https://doi.org/10.1242/dev.073452
SAS. (2012). Statistical Analysis System, User's Guide. Statistical, Version 9.1th ed. SAS. Inst. Inc. Cary. N.C.
Sharif, F., Steenbergen, P. J., Metz, J. R., & Champagne, D. L. (2015). Long-lasting effects of dexamethasone on immune cells and wound healing in the zebrafish. Wound Repair and Regeneration, 23(6), 855-865.
https://doi.org/10.1111/wrr.12366
Schorpp-Kistner, M., Z. Q. Wang, P., & Angel, E. F. (1999). JunB is essential for mammalian placentation. The EMBO Journal, 18, 934-948.
https://doi.org/10.1093/emboj /18.4.934
Stoick, C. L., Moon, R. T., & Weidinger, G. (2007). Advances in signaling in vertebrate regeneration as a prelude to regenerative medicine. Genes & Development, 21, 1292-1315.
https://doi.org/10.1101/gad.1540507
Vegiopoulos, A., & Herzig, S. (2007). Glucocorticoids, metabolism and metabolic diseases. Molecular and Cellular Endocrinology, 275, 43-61.
https://doi.org/10.1016/j.mce.2007.05.015
Wang, J., Ho, S., Liu, Y. Lee, S. C., Liu, Y. C., Liao, Y. C., & Ho, C. M. (1999). Dexamethasone reduces nausea and vomiting after laparoscopic cholecystectomy. British Journal of Anaesthesia, 83(5), 772-774.
https://doi.org/10.1093/bja/83.5.772
Weber, C. M., Martindale, M. Q., Tapscott, S. J., & Unguez, G. A. (2012). Activation of Pax7-positive cells in a non-contractile tissue contributes to regeneration of myogenic tissues in the electric fish S. macrurus. PLoS One, 7(5).
https://doi.org/10.1371/journal.pone.0036819
Yin, V. P., & Poss, K. D. (2008). New regulators of vertebrate appendage regeneration. Current Opinion in Genetics & Development, 18(4), 381-386.
https://doi.org/10.1016/j.gde.2008.06.008
Yoshida, H., Okada, M., Takebayashi-Suzuki, K., Ueno, N., & Suzuki, A. (2016). Involvement of JunB proto-oncogene in tail formation during early Xenopus embryogenesis. Zoological Science, 33(3), 282-289.
https://doi.org/10.2108/zs150136
Yoshinari, N., Ishida, T., Kudo, A., & Kawakami, A. (2009). Gene expression and functional analysis of zebrafish larval fin fold regeneration. Developmental Biology, 325(1), 71-81.
https://doi.org/10.1016/j.ydbio.2008.09.028
Zenz, R., Eferl, R., Kenner, L., Florin, L., Hummerich, L., Mehic, D., Scheuch, H., Angel, P. E., Tschachler, E., & Wagner, E. F. (2005). Psoriasis-like skin disease and arthritis caused by inducible epidermal deletion of Jun proteins. Nature, 437, 369-375.
https://doi.org/10.1038/nature03963
Zenz, R., Eferl, R., Scheinecker, C., Redlich, K., Smolen, J., Schonthaler, H. B, Kenner, L., Tschachler, E., & Wagner, E. F. (2008). Activator protein 1 (Fos/Jun) functions in inflammatory bone and skin disease. Arthritis Research & Therapy, 10, 201.