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Teleost fish

Cheshenko, K., Pakdel, R, and Segner, H. et al. (2008). Interference of endocrine disrupting chemicals with aromatase CYP19 expression or activity, and consequences for reproduction of teleost fish. General and Comparative Endocrinology 155, 31-62. [Pg.342]

Piferrer, F. (2001). Endocrine sex control strategies for the feminization of teleost fish. Aquaculture 197, 229-281. [Pg.364]

Calcium influx Immune Teleost fish — Increased Burnett (1997)... [Pg.155]

Sastry, K.V. and K. Sunita. 1983. Enzymological and biochemical changes produced by chronic chromium exposure in a teleost fish, Channa punctatus. Toxicol. Lett. 16 9-15. [Pg.123]

Venugopal, N.B.R.K. and S.L.N. Reddy. 1992b. Nephrotoxic and hepatotoxic effects of bivalent and hexavalent chromium in a teleost fish Anabas scandens enzymological and biochemical changes. Ecotoxicol. Environ. Safety 24 287-293. [Pg.125]

Hogstrand, C. 1991. Regulation of metallothionein in teleost fish during exposure. Ph.D. dissertation. Univ. Goteborg, Goteborg, Sweden. 176 pp. [Pg.222]

Ram, R.N. 1988. Carbofuran-induced histophysiological changes in thyroid of the teleost fish, Channa punctatus (Bloch). Ecotoxicol. Environ. Safety 16 106-113. [Pg.825]

Mishra, J. and A.K. Srivastava. 1984. Effects of chlordane on the blood and tissue chemistry of a teleost fish, Heteropneustes fossilis. Cell. Mol. Biol. 30 519-523. [Pg.882]

Electron paramagnetic resonance (EPR) examination of hepatic microsomes from differently pretreated animals has lead to the conclusion that MC pretreatment leads to the formation of cytochrome P-1+50 (P-1+1+8) with high spin iron (6, 1+6). Chevion et al. (28) failed to demonstrate the presence of high spin cytochrome P-1+50 in a teleost fish even after induction with MC. The work of Chevion et al. (28 ) indicates further that the fish cytochrome P-1+50, which is inducible with PAH s and metabolizes readily PAH s, is not identical with the mammalian cytochrome P-1+1+8. [Pg.285]

Chevion, M., Stegeman, J.J., Peisach, J. and Blumberg, W.E. Electron paramagnetic resonance studies on hepatic microsomal cytochrome P- 50 from a marine teleost fish. Life Sci. (1977) 20, 895-900. [Pg.292]

Since this structure was first proposed, Braunitzer and co-workers have determined the amino acid sequence of rhinoceros hemoglobin (23a). Its allosteric effector site shows only a single substitution compared to that of human hemoglobin—His NA2/8 — Glu—yet ATP lowers its oxygen affinity more than DPG, and GTP lowers it more than ATP, just as in teleost fish (R. Baumann, unpublished observations). This observation supports the hydrogen bond between N-6 of the adenine and Glu NA2 proposed in Fig. 6 in fact it can hardly be explained without that bond. [Pg.221]

Sastry, K.V. and Agrawal, M.K. Mercuric chloride induced enzymological changes in kidney and ovary of a teleost fish, Channapunctatus, Bull Environ. Contam. Toxicol, 22(l/2) 38-43, 1979. [Pg.1719]

Figure 7 shows the effect of ectopic administration of T3 to the developing zebrafish embryo. At nontoxic concentration (50 nM), only a moderate fraction (less than 5%) of the zebrafish transcriptome shows significant changes. Ossification, visual processes, and the hematopoietic system were the physiological processes most affected by the treatment, in a pattern consistent with an advancement of the development in these particular functions (Fig. 7b). Genes involved in these three processes are known targets for TDCs during metamorphosis in amphibians, teleost fishes, and lampreys [54—60], and constitute molecular counterparts of different endpoints used to test for TDC in amphibians [56, 58]. Therefore, they are excellent candidates for markers of thyroid disruptors in zebrafish at early developmental stages. Chapter 14 provides a more in-deep description of the developmental effects of thyroid disruption in zebrafish embryos. Figure 7 shows the effect of ectopic administration of T3 to the developing zebrafish embryo. At nontoxic concentration (50 nM), only a moderate fraction (less than 5%) of the zebrafish transcriptome shows significant changes. Ossification, visual processes, and the hematopoietic system were the physiological processes most affected by the treatment, in a pattern consistent with an advancement of the development in these particular functions (Fig. 7b). Genes involved in these three processes are known targets for TDCs during metamorphosis in amphibians, teleost fishes, and lampreys [54—60], and constitute molecular counterparts of different endpoints used to test for TDC in amphibians [56, 58]. Therefore, they are excellent candidates for markers of thyroid disruptors in zebrafish at early developmental stages. Chapter 14 provides a more in-deep description of the developmental effects of thyroid disruption in zebrafish embryos.
MacKenzie DS, Jones RA, Miller TC (2009) Thyrotropin in teleost fish. Gen Comp Endocrinol 161 83-89... [Pg.432]

Sorensen, P. W., and Stacey, N. E. (1990). Identified hormonal pheromones in the goldfish the basis for a model of sex pheromones function in teleost fish. In Chemical Signals in Vertebrates, vol. 6, ed. R. L. Doty and D. Miiller-Schwarze, pp. 302-311. New York Plenum. [Pg.514]

Mori, M., Hikichi, S., Kamiya, H., and Hashimoto, Y. (1972). Three species of teleost fish having diacyl glyceryl ethers in the muscle as a major lipid. Bull. Jpn. Soc. Sci. Fisheries 38, 56-63. [Pg.49]

Studies on teleost fish and mammals have demonstrated the existence of non-rod, non-cone ocular photoreceptors. In the case of VA opsin in the roach, electrophysiological evidence suggests that one function of this photosensory photopigment is to modulate the activity of retinal horizontal cells. To what end remains unclear, but this fits with the general role of horizontal cells in the teleost... [Pg.17]

Sturm, A., Da Silva de Assis, H.C., Hansen, P.D. (1999). Cholinesterases of marine teleost fish enzymological characterization and potential use in the monitoring of neurotoxic contamination. Marine Environmental Research, 47 ... [Pg.136]


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