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1.
The presence of outer ring deiodinating (ORD) and inner ring deiodinating (IRD) activities was investigated in different tissues of Oreochromis niloticus (Nile tilapia), Clarias gariepinus (African catfish), Oncorhynchus mykiss (rainbow trout) and halmus maximus (turbot). High-Km rT3 ORD is present in the kidney of most of the fishes studied, except in catfish. In turbot, besides the kidney, rT3 ORD is also present in liver, heart and ovary. Low-Km T4 ORD is found in the liver and low-Km T3 IR the brain of all the fishes studied. In addition, low levels of low-Km T3 IRD were demonstrated in gill and skin of Nile tilapia, liver of rainbow trout and gill and kidney of turbot. For the different teleosts, the biochemical properties of the different rT3-deiodinating enzymes mentioned, T4 ORD in liver and T3 IRD in brain and tilapia gill were compared to those of the deiodinases formerly characterized in Oreochromis aureus (blue tilapia). In general, the different deiodinases demonstrate analogous sensitivities to iodothyronines and inhibitors, although minor differences occur. The various deiodinating enzymes all depend on addition of dithiothreitol and demonstrate maximal activity pH between 6.5 and 7. The optimal incubation temperature of rT3 ORD and T4 ORD in tilapia and catfish is 37 °C, in trout and turbot it varies, depending on the tissue, between 25 ° and 37 °C. For the different T3 IRD activities the optimal temperature is 37 °C in warmwater as well as in coldwater species. The apparent Km values for rT3 ORD lay in the M range, for T4 ORD and T3 IRD they lay in the nM range. Vmax values are usually higher in tilapia as compared to the other teleosts studied. Based on the similarities in susceptibility to inhibition by different iodothyronines and inhibitors and the agreement of the apparent Km values, we conclude that the deiodinating enzymes in teleosts are more similar to mammalian deiodinases than is generally accepted.  相似文献   

2.
Channel catfish (Ictalurus punctatus) in pond culture, sampled once per day, have been reported to exhibit significant seasonal cycles in the thyroid hormones thyroxine (T4) and 3,5,3′-triiodothyronine (T3), rising from levels generally below 2 ng/ml in January to above 8 ng/ml in July. To determine if daily thyroid hormone cycles underlie these seasonal changes, we blood sampled groups of 20 catfish (10 males and 10 females) in the morning (approx. 1 h after sunrise), midday, and evening (approx. 1.5 h before sunset) on January 9, April 4, and July 29. From January to July, pond temperatures rose from 7 ° to 32 °, associated with significant (p < 0.05) increases in mean fish weight (from 477 to 1052 g) and in monthly mean food consumption (from 34 to 474.7 g/kg fish). On all three dates, significantly (p < 0.05) greater levels of both hormones (except T3 in April) were found in midday and evening compared to morning samples. In January, the daily change was small (from morning to midday, mean T3 rose from 2.2 to 3.6 ng/ml and mean T4 from 2.3 to 4.8 ng/ml), whereas in July it was considerably greater (from morning to evening, mean T3 rose from 7.2 to 17.8 ng/ml, and T4 from 9.0 to 22.4 ng/ml). No significant differences were found between midday and evening levels, or between males and females. Additionally, no seasonal phase-shifting of cycles was apparent. A subset of animals was examined to evaluate the potential contribution of peripheral mechanisms in generating these seasonal and daily cycles. Whereas we observed only minor changes in thyroid hormone binding to plasma proteins during any single day, a significant seasonal increase in the ratio of free T4:free T3 indices (from a mean of 1.3–1.5 in January to 2.0–2.1 in July) indicated enhanced T3 binding by plasma proteins in July. Furthermore, in vitro hepatic T4 and T3 deiodination activities showed across dates no significant change in T4 outer-ring deiodination to produce T3 (ranging from a mean of 53.1 to 70.1 pmol T4 deiodinated/h/mg microsomal protein), but a significant (p < 0.05) decrease in T4 inner-ring deiodination to degrade T4 to 3,3′5′-triiodothyronine (from a mean in January of 2.4 to 0.65 pmol T4 deiodinated /h/mg protein in April) and a significant (p < 0.05) decrease in T3 inner-ring deiodination to degrade T3 to 3,3′-diiodothyronine (from a mean in January of 115.5 to 3.1 pmol T4 deiodinated/h/mg protein in July). These results demonstrate that channel catfish under conditions of natural temperature and photoperiod exhibit robust daily cycles in total plasma T4 and T3 similar in magnitude to those reported for other fish species held under controlled laboratory conditions. These cycles maintain a similar phase throughout the year, indicating that apparent seasonal increases in thyroid hormones are not due to phase-shifting of daily cycles. However, seasonal studies sampling fish only in the morning would underestimate the magnitude of the annual changes in blood thyroid hormones. Thyroidal status, as judged from total plasma T4 and T3 levels in the afternoon, is greatest in July, coinciding with the postspawning peak in food consumption and growth. Enhanced T3 plasma protein binding and a shift from predominantly hepatic inner-ring deiodination in winter to outer-ring deiodination in summer suggest that peripheral mechanisms contribute to the generation of these seasonal changes.  相似文献   

3.
Brown (BT) and rainbow trout (RT) in freshwater (FW) were treated with ovine growth hormone (GH), GH + iopanoic acid (IOP), and GH + IOP plus triiodothyronine (T3) for RT only. After 1 week of treatment, trout were transferred to 30 o/oo SW and treatment continued. In FW, GH treatment increased significantly plasma T3 level (BT) and T3/T4 ratio (BT and RT) by stimulating T4 to T3 deiodination. In the GH + IOP group, the plasma T3 levels and T3/T4 ratio fell significantly as T4 to T3 deiodination was inhibited. In GH + IOP + T3-treated RT, plasma T3 and T3/T4 ratios increased significantly relative to other groups. No mortality occurred and plasma osmolarity (PO) was not altered by any treatment in FW. After transfer to SW, all IOP + GH trout died within 2 (BT) or 3 days (RT). All GH-treated or control BT survived to the end of the experiment (6 days). RT survival rates tended to be improved in GH and GH + IOP + T3 groups relative to controls. Correlatively on day 1 the PO increase was significantly higher in IOP + GH groups (BT and RT) than in the other groups and significantly lower in GH and GH + IOP + T3 treated RT than in controls from days 1 to 6. These data confirm the requirement of T3 and deiodination of T4 to T3 for the development of hypoosmoregulatory mechanisms in SW as previously shown (Lebel and Leloup 1992). Furthermore, the suppression of the hypoosmoregulatory effect of GH, when conversion of T4 to T3 was inhibited by IOP and the reversal when T3 was added to IOP + GH treatment suggests that GH osmoregulatory action in SW acts via the simulation of T4-5′ monodeiodination which increases T3 production.  相似文献   

4.
Tissue T3 (3,5,3′-triiodo-L-thyronine) concentrations were measured in rainbow trout, Salmo gairdneri, after digestion by Pronase or collagenase and extraction with ethanolic ammonia (99:1, v/v) followed by 2N NH4OH and chloroform. Recoveries of [125I]T3 administered in vivo or in vitro were high and consistent and there was close parallelism between sample dilutions and the radioimmunoassay curve, but recoveries of unlabeled T3 administered in vitro were low and variable. Alternatively, trout were brought to isotopic equilibrium by [125I]T3 infusion for 96 h, the extracted [125I]T3 determined by gel filtration and the tissue T3 content calculated from the specific activity of plasma [125I]T3. By the latter method, tissue T3 concentrations were: intestine (4.2 ng/g), kidney (2.5), liver (2.8), stomach (1.5), heart (1.0), muscle (0.7), gill (0.6) and skin (0.3). Muscle (67% of body weight) comprised the largest tissue T3 pool (82% of all tissues examined). Seven days exposure of trout to water acidified with H2SO4 (pH 4.8) or acidified water containing aluminum (21.6 mM), decreased tissue T3 content generally and particularly in muscle (14% of controls). In conclusion, skeletal muscle is the largest T3 tissue pool and seems highly responsive to altered physiologic state.  相似文献   

5.
Fasting and refeeding have considerable effects on thyroid hormone metabolism. In tilapia (Oreochromis niloticus), fasting results in lower plasma T3 and T4 concentrations when compared to the ad libitum fed animals. This is accompanied by a decrease in hepatic type II (D2) and in brain and gill type III (D3) activity. No changes in kidney type I (D1) activity are observed. Refeeding results in a rapid restoration of plasma T4 values but not of plasma T3. Plasma T3 remains low for two days of refeeding before increasing to normal levels. Liver D2 and gill D3 also do not increase until two days after refeeding. Brain D3, on the other hand, rises immediately upon refeeding. These results suggest that the change in hepatic D2 activity is one of the main factors responsible for the changes in plasma T3 observed during starvation and refeeding in tilapia. This finding supports the hypothesis that, in contrast to mammals and birds, liver D2 is the primary source of plasma T3 in fish. Although the deiodinases important for the gross regulation of plasma T3 during fasting/refeeding differ (mammals: D1 and D3, birds: D3, fish: D2), they all occur in the liver, suggesting that the organ itself may play a crucial role. In addition, the changes in brain and gill D3 suggest that these enzymes constitute a fine tuning mechanism for regulation of T3 availability at the cellular or plasma levels, respectively.  相似文献   

6.
With the aim of comparing the effects of oral T3 and NaCl administration on trout hypoosmoregulatory mechanisms, three groups of rainbow trout (Oncorhynchus mykiss Walbaum) held in freshwater (FW) were fed a basal diet (C), the same diet containing 8.83 ppm of 3,5,3-triiodo-L-thyronine (T3) (T) or 10% (w/w) NaCl (N) respectively for 30 d. They were then transferred to brackish water (BW) for 22 d and fed on diet C. Gill (Na++K+)-ATPase activity and its dependence on ATP, Na+ and pH, number of gill chloride cells (CC), serum T3 level as well as fish growth, condition factor (K) and mortality were evaluated. During the FW phase, as compared to C trout, T trout showed a two fold higher serum T3 level, had unchanged gill (Na++K+)-ATPase activity and increased CC number, whereas N trout showed higher gill (Na++K+)-ATPase activity and CC number. At the end of the experiment the enzyme activity was in the order T>N>C groups and all groups showed similar CC number. Both treatments changed the enzyme activation kinetics by ATP and Na+. A transient increase in K value occurred in N group during the period of salt administration. In BW, T and N groups had higher and lower survival than C group respectively. Other parameters were unaffected by the treatments. This trial suggests that T3 administration promotes the development of hypoosmoregulatory mechanisms of trout but it leaves the (Na++K+)-ATPase activity unaltered till the transfer to a hyperosmotic environment.  相似文献   

7.
Rainbow trout Oncorhynchus mykiss Walbaum were fed a pelleted diet (14.3% wet weight lipid) containing 9 p.p.m. 3, 5, 3′‐triiodo‐l ‐thyronine (T3) for 1 month and then transferred from fresh water to brackish water (average 22 p.p.t. salinity), where they were maintained untreated for 22 days. Trout fed a control diet were subjected to the same protocol. For both treated and control trout, liver lipid and fatty acid composition, mitochondrial respiratory activity and oxidative phosphorylation and (Na+ + K+)‐ATPase activity were monitored in fish sampled periodically throughout the trial. No differences between treated and control trout occurred in liver total lipid, phospholipid and cholesterol content or fatty acid composition. Conversely, irrespective of T3 administration, the trout from the two habitats showed adaptive changes to salinity, differing in phospholipids and in the fatty acid composition of total and neutral lipids and selected phospholipids. Liver membrane permeability and mitochondrial respiratory activity were affected by both T3 treatment and salinity transfer. The latter was apparently greater than the former in affecting mitochondrial respiratory activity. The higher (Na+ + K+)‐ATPase activity in T3‐treated trout after 22 days in brackish water may reflect long‐term effects of the hormone linked to salinity adaptation.  相似文献   

8.
The absorptions of 3,5,3-triiodo-L-thyronine (T3) and L-thyroxine (T4) from the intestinal lumen of the rainbow trout were compared in vivo. Tracer doses of [125I]T4 (+T4) or [125I]T3 (*T3) were injected through an anal cannula into the duodenum of trout fasted for 3 days at 12°C, and radioactivity was measured in blood and tissues at 4–48 h. *T3 was removed more extensively than *T4 from the intestinal lumen and more radioactivity was absorbed into the blood and tissues of u+T3-injected trout than *T4-injected trout. HPLC analysis showed that a high proportion of the radioactivity in the plasma, liver, kidney and intestinal lumen of *T3-injected trout remained as the parent *T3. However, in *T4-injected trout most plasma radioactivity was in the form of 125I–, and by 24 h a high proportion of luminal radioactivity was 125I–. By 48 h, over 4% of the injected *T3 and 1% of the injected *T4 dose resided in the gall bladder, primarily as derivatives of *T3 or *T4. We conclude that T3 is absorbed more effectively than T4 from the intestinal lumen of fasted trout, indicating the potential for an enterohepatic T3 cycle.  相似文献   

9.
The acute and chronic effects of excess iodide (KI or NaI) were studied on thyroid function of rainbow trout at 11±1°C. No Wolff-Chaikoff effect, characteristic of mammals, was observed and instead plasma L-thyroxine (T4) levels increased 6 hr after a single iodide injection. Plasma 3,5,3′-triiodo-L-thyronine (T3) did not change and by 24 hr plasma T4 returned to normal. This iodide-induced elevation in plasma T4 was probably not due to toxic effects demonstrated at higher NaI or KI doses. A single iodide injection also decreased the plasma iodide distribution space, decreased the fractional rate of plasma iodide loss and completely blocked thyroidal uptake of radioiodide. Injections of iodide over a 22-day period elevated plasma iodide 200X with no mortality and no influence on plasma T4 or T3. It is concluded that: (i) apart from the transient 6h increase in plasma T4, trout thyroid function, as judged by plasma hormone levels, is insensitive to considerable iodide excess, (ii) non-invasive iodide suppression of thyroidal radioiodide recycling may be useful in kinetic studies of125I-labeled thyroid hormones, and (iii) fundamental differences in intrathyroidal iodine metabolism appear to exist between mammals and fish.  相似文献   

10.
Plasma levels of L-thyroxine (T4) and 3,5,3-triiodo-L-thyronine (T3) and the percentage of plasma T4 and T3 present in the free (dialyzable) form (%FT4 and %FT3) were measured in 16 species (11 families) of tropical marine teleosts from an inshore Barbados reef. Mean plasma T4 varied from 0.2 ng/ml to 42 ng/ml; mean plasma T3 varied from < 0.2 ng/ml to 50 ng/ml. The highest T4 and T3 levels were recorded in parrot-fish and the lowest levels in filefish. The %oFT4 and %FT3 varied from 0.05–3.41%. Estimated levels of plasma free T4 and free T3 levels ranged from 0.4–466 pg/ml. The extremely wide inter- and intra-species ranges in levels of free T4 and T3 do not support a previous suggestion, based on temperate freshwater salmonid species, that free T4 and T3 levels in fish may fall within a relatively range narrow comparable to that of homeothermic vertebrates.  相似文献   

11.
An assay method based on thin layer chromatography to study the arachidonic acid (AA) metabolism in gill tissues was optimized and the effect of osmotically different incubation mediums on AA metabolism was evaluated. Rainbow trout gill tissues metabolize AA into PGE2 in highest concentration followed by PGD2, PGF2 and 6-keto-PGF1 (the stable metabolite of PGI2) among the prostanoids tested. Approximately 40% of PGE2 is synthesized within the first minute of incubation and is directly dependent on the substrate concentration (AA). As in mammalian tissues, PGE2 synthesis in fish gills is inhibited by the cyclooxygenase inhibitor indomethacin. PGE2 synthesis in gill homogenate and isolated gill cells incubated in trout Ringer was 0.45 and 1.9 ng/mg protein, respectively, and increased to 8.9 and 4.3 ng/mg protein, respectively, when incubated in KPO4 buffer, due to a ten-fold increase in the free AA. The hydroxy acid synthesis of the gill homogenate was higher (13%), and that of the isolated gill cells incubated in KPO4 buffer was lower (44%) compared to gill homogenate and cells incubated in trout Ringer. Gill homogenate incubated in 50 mM phosphate buffer with increasing sodium or potassium concentrations (up to 250 mM) exhibited a concentration-dependent increase in PGE2 synthesis (220% and 72%, respectively). Prolactin stimulated the PGE2 synthesis up to 30% while PGD2, PGF2 and 6-keto-PGF1 synthesis was not affected. This effect of prolactin was maximal when PGE2 synthesis was estimated 30 minutes after prolactin addition and diminished after two hours. These results suggest that rainbow trout gills possess the ability to metabolize AA through the cyclooxygenase and lipoxygenase pathways. PGE2 synthesis may be under the influence of ion balance and prolactin availability, indicating the probable involvement of AA metabolites in the regulation of ion balances across the gill membrane.  相似文献   

12.
The 5′-monodeiodinase (5′-MDA) activity was measured in liver slices that were incubated for 3 hours with epinephrine (E) or norepinephrine (NE) in order to examine the influence of these catecholamine hormones on the regulation of hepatic monodeiodination of thyroxine (T4) in rainbow trout. Both E and NE induced a dose-dependent increase in 5′-MDA activity and in addition, E stimulated the release of T3 into the medium. In liver slices taken from trout that had been treated with the β-adrenoceptor inhibitor propranolol, the response to both E and NE was attenuated. The findings provide evidence of an action of these catecholamine hormones on the peripheral regulation of T3 production, and suggest that the control operatesvia the β-adrenoceptors. Corresponding author.  相似文献   

13.
The diurnal rhythms of plasma glucose, cortisol, growth hormone (GH) and thyroid hormone (T4, T3) concentrations and hepatic glycogen content were measured in rainbow trout that had been entrained to a specific time of daily feeding (post-dawn, midday, pre-dusk); the purpose of the study was to investigate the significance of feeding time on hormones and metabolite patterns. Plasma GH, cortisol and T4 concentrations all showed evidence of a diurnal rhythm in some treatment groups. There was a significant interaction between the time of feeding and plasma GH and cortisol concentration rhythms; for GH, this appeared to be related to the phase-shifting of the post-prandial increases in plasma GH concentrations, and for cortisol, the rhythms were only evident in fish fed in the post-dawn period [diurnal rhythms were not evident in treatment groups fed in at midday or pre-dusk]. Peak plasma T4 concentrations were evident during the photophase in all three treatment groups; however, the time of feeding had a negligible effect on the timing of those peaks. There were no apparent diurnal rhythms of plasma T3 and glucose concentrations, hepatic glycogen content or hepatosomatic index in any of the three treatment groups. To whom correspondence should be addressed  相似文献   

14.
Rainbow trout fed a 26% canola meal-based (CM) diet for 12 weeks at 15°C exhibited reduced growth, lower feed conversion, enlarged thyroid glands and lower plasma thyroid hormone (TH) levels than comparable fish fed equinitrogenous, equicaloric soybean meal-based (SB) diets. Supplementation of the SB diets with either T4 (20 mg/kg) or T3 (10 or 20 mg/kg) had no effect on the growth rate, feed conversion and thyroid histology of the trout. However, plasma T4 levels weredepressed in trout fed the T4- and high T3-supplemented SB diets. In trout fed T4- and T3-supplemented CM diets the growth rates and feed conversion were not significantly different from those of the SB-fed groups. Moreover, in the T4-supplemented group, plasma T4 levels were in the normal range. However, thyroid enlargement was evident in all the CM-fed fish, and plasma T3 levels were markedly elevated in groups fed the T3-supplemented CM diets. The data suggest that antithyroid components in the CM diets inhibited TH synthesis (but not their release), and impaired TH clearance from the circulation. There were no significant differences in plasma cortisol levels in the 8 treatment groups, nor were there differences in the histological appearance of the interrenal gland. However, when the data from SB- and CM-fed fish were pooled, plasma cortisol levels in the SB-fed fish were significantly lower than in the CM-fed animals. Glucosinolates at a level of 164 mg/kg diet were toxic to young trout, but the effect was ameliorated by dietary TH supplementation.  相似文献   

15.
Juvenile rainbow trout, held at 12°C on a 12 h light :12 h dark photocycle, were fed a constant ration (1 % of body wt day ?1) of isonitrogenous and isoenergetic diets that varied in either arginine content (3.6-56.1 g kg?1 dry matter; experiment 1), or glycine (3.3–118 g kg?1 dry matter) and alanine (5.0-42.3 g kg?1 dry matter) content (experiment 2). In experiment 1, the lowest dietary level of arginine depressed growth, feed efficiency, plasma l -thyroxine (T4) and 3,5,3′-triiodo-l -thyronine (T3) levels and hepatic T4 5’monodeiodinase (5'D) activity responsible for T4-to-T3 conversion. Over the dietary range of 7.1–56.1 g arginine kg?1, there was no change in 5'D activity, despite an arginine stimulation of growth. The optimum level of arginine for growth was within the range of 14.1–28.1 g kg?1 of the diet or 32–63 g kg?1 of dietary protein. In experiment 2, an increase in dietary glycine level, at the expense of glutamic acid, increased 5'D activity without attendant elevation of the plasma T3 level. The latter finding suggests that glycine also induced a compensatory increase in T3 degradation rate. This may explain why the glycine-induced increase in 5'D activity was unaccompanied by any changes in growth indices. Alteration of dietary alanine content did not affect growth or thyroid function. We conclude that of the various dietary amino acids tested, only glycine led to a progressive stimulation of hepatic T4 5'D activity. However, because glycine likely enhanced T3 degradation, no increases in plasma T3 or growth indices were found. Glycine may serve as an advance signal that activates thyroid function immediately preceding or coincident with energy and nutrient (especially protein) intake. This, in turn, may improve the efficiency of nutrient absorption and/or post-absorptive anabolic events.  相似文献   

16.
Extrathyroidal T4 5′-monodeiodination, demonstrated in several teleost species, generates T3 which binds more effectively than T4 to putative nuclear receptors and is probably the active thyroid hormone. T4 to T3 conversion is sensitive to the physiological state and provides a pivotal regulatory link between the environment and thyroid hormone action. T3 generation is enhanced in anabolic states (positive energy balance or conditions favoring somatic growth; food intake or treatment with androgens or growth hormone) and is suppressed in catabolic states (negative energy balance or conditions not favoring somatic growth; starvation, stress, or high estradiol levels associated with vitellogenesis). In fish, as in mammals, thyroidal status may be finely tuned to energy balance and through T3 production regulate energy-demanding processes, which in fish include somatic growth, development and early gonadal maturation.  相似文献   

17.
Four separate 8-week feeding trials were conducted to assess the effects of supplementing semipurified diets with either triiodothyronine (T3) or thyroxine (T4) at 0, 2, 10, and 50 mg/kg on growth and body composition of juvenile red drum (Sciaenops ocellatus) held in artificial brackish water (6‰) and artificial seawater (32‰). At both levels of salinity, increasing doses of T3 resulted in fish with reduced weight gain, feed efficiency, condition factor (weight × 100/length3), and muscle ratio (muscle weight × 100/body weight), as well as a lighter body color. Significant (p < 0.05) effects of T3 on the proximate composition of whole body, liver, and muscle were variable, generally reflecting decreased lipid and protein storage in liver and muscle, respectively. The two highest doses of T3 given to seawater adapted fish increased survival. Dietary T4 supplementation had no distinctive effects on appearance, growth or proximate body composition. These results indicate that whereas T3 may function to regulate protein and lipid metabolism in red drum, dietary supplementation with T3 leads to a hyperthyroidism-induced catabolic state. The elevated endogenous thyroid hormone levels found in fish fed optimal diets may thus adequately supply tissue needs during juvenile growth.  相似文献   

18.
The capacity of cortisol, ovine growth hormone (oGH), recombinant bovine insulin-like growth factor I (rbIGF-I) and 3,3,5-triiodo-l-thyronine (T3) to increase hypoosmoregulatory capacity in the euryhaline teleost Fundulus heteroclitus was examined. Fish acclimated to brackish water (BW, 10 ppt salinity) were injected with a single dose of hormone suspended in oil and transferred to seawater (SW, 35 ppt salinity) 10 days post-injection. Fish were sampled 24 h after transfer and plasma osmolality and gill Na+, K+-ATPase activity were examined. Transfer from BW to SW induced significantly increased plasma osmolality but not gill Na+, K+-ATPase activity. Cortisol (50 g g–1 body weight) improved the ability to maintain plasma osmolality and to increase gill Na+, K+-ATPase activity. oGH (5 g g–1 body weight) also increased hypoosmoregulatory ability and gill Na+, K+-ATPase activity. A cooperation between oGH and cortisol was observed in increasing hypoosmoregulatory ability but not in increasing gill Na+, K+-ATPase activity. rbIGF-I (0.5 g g–1 body weight) alone was without effect in increasing salinity tolerance or gill Na+, K+-ATPase activity. rbIGF-I and oGH showed a positive interaction in increasing salinity tolerance, but not gill Na+, K+-ATPase activity. Treatment with T3 (5 g g–1 body weight) alone did not increase salinity tolerance or gill Na+, K+-ATPase activity, and there was no consistent significant interaction between cortisol and T3 or between GH and T3. The results confirm the classical role of cortisol as a seawater-adapting hormone and indicate an interaction between cortisol and the GH/IGF-I axis during seawater acclimation of Fundulus heteroclitus.  相似文献   

19.
The in vitro hepatic 5′-monodeiodination of thyroxine (T4) to triiodothyronine (T3) in Oreochromis mossambicus, Channa striata, Clarias batrachus, Cyprinus carpio and Oxyeleotris marmorata was found to be time, pH and temperature dependent, and related to the amount of substrate (T4) and homogenate introduced into the reaction vessel, in a manner which was consistent with Menton-Michaelis kinetics, and thus indicative of an enzyme-regulated process. Dithiothreitol introduced into the reaction vessel stimulated T3 production in a dose-related manner. Hepatic 5′-monodeiodinase activity was also detected in a further 28 species of teleosts suggesting that the peripheral monodeiodination of T4, which is well-documented in salmonids, is also widespread amongst other teleost fishes. All species examined exhibited evidence of enzymatic deiodination, but there were marked differences in Km and Vmax values between the species. There was no apparent phylogenetic or environmental relationships to explain the widely divergent Km and/or Vmax values, nor was there a correlation between Km and Vmax when the species were considered together.  相似文献   

20.
A factorial experiment was conducted to determine the effect and interaction of dietary carbohydrate level and triiodo-L-thyronine (T3) supplementation on the growth, physiological response and plasma insulin and cortisol levels of rainbow trout. The oral administration of T3 significantly increased the growth, protein efficiency ratio and feed efficiency of trout, indicating an increased protein and perhaps energy utilization in these fish. However, T, administration did not significantly increase the utilization of dietary glucose as an energy source by the trout. Similarly, the administration of T3 did not significantly affect plasma insulin levels in either the fed or the fasted trout. Plasma insulin levels were significantly higher in fed trout reared on the non-T3 supplemented high carbohydrate diet in comparison to trout reared on the low carbohydrate diets. This indicates that increased dietary carbohydrate stimulates increased insulin secretion in the trout. Therefore, although rainbow trout are not insulin-deficient, they can still be considered a diabetic-like animal due to their poor glucose tolerance. Plasma cortisol levels were not affected by diet composition and altered plasma glucose levels.  相似文献   

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