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  • 1
    Publication Date: 1990-11-01
    Print ISSN: 0302-766X
    Electronic ISSN: 1432-0878
    Topics: Biology , Medicine
    Published by Springer
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  • 2
  • 3
    Publication Date: 1987-07-13
    Print ISSN: 0014-5793
    Electronic ISSN: 1873-3468
    Topics: Biology , Chemistry and Pharmacology
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  • 4
    ISSN: 1573-5168
    Keywords: IGF-I mRNA ; solution hybridization assay ; tissue distribution ; growth hormone ; somatolactin ; prolactin ; hepatocyte ; fish ; Oncorhynchus kisutch
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Résumé Afin d'étudier les régulations homronales et nutritionnelles de l'expression des ARNm de l'IGF-I (insulin-like growth factor I), un dosage spécifique par hybridation en solution des ARNm d'IGF-I de saumon coho et protégé des RNases, a été développé. Ce dosage, à la fois rapide et sensible, présente un faible coefficient de variation inter- (〈 15%) et intra- (〈 5%) dosage. L'étude de la distribution tissulaire des ARNm de l'IGF-I et des effets de l'hormone de croissance (GH), de la prolactine (Prl) et de la somatolactine (SI) sur l'expression hépatique des ARNm de l'IGF-I, a été entreprise in vivo chez le saumon coho en utilisant ce dosage. Le foie présente les plus grandes quantités d'ARNm d'IGF-I (16 pg/μg d'ADN). Des quantités significatives d'ARNm d'IGF-I ont été également détectées dans tous les autres tissus étudiés (intestin 4,1; rein 3,8; branchie 2,4; ovaire 2,3; muscle 2,1; rate 1,7 et graisse 1,1 pg/μg d'ADN). L'injection à des saumons coho, de GH à des doses de 0,1 et 1 μg/g de poids vif, augmente significativement et de manière dose dépendante les niveaux hépatiques d'ARNm d'IGF-I. L'injection de SI de saumon coho, un membre récemment découvert de la famille GH/Prl, stimule avec la plus haute dose utilisée, l'expression des ARNm d'IGF-I alors que la Prl n'a aucun effet. La GH augmente de manière dose dépendante (0,01–1 μg/ml) l'expression in vitro des ARNm d'IGF-I par des ARNm d'IGF-I par des hépatocytes de saumon coho en culture. Ces résultats indiquent que, chez le saumon coho, l'expression des ARNm d'IGF-I est présente dans le nombreaux tissus et que, l'expression hépatique est, au moins en partie, régulée par la GH et peut-être par d'autres hormones. Le dosage par séquence spécifique mise au point dans le présent travail, peut-être utilisé pour la quantification précise des ARNm, d'IGF-I de salmonidés et devrait permettre une meilleure connaissance de la physiologie de L'IGF-I chez les salmonidés.
    Notes: Abstract To examine the hormonal and nutritional regulation of insulin-like growth factor I (IGF-I) mRNA expression, a sequence-specific solution hybridization/RNase protection assay for coho salmon IGF-I mRNA was developed. This assay is both rapid and sensitive and has low inter- (less than 15%) and intra-assay variations (less than 5%). Using this assay, the tissue distribution of IGF-I mRNA and effects of growth hormone (GH), prolactin (PRL) and somatolactin (SL) on hepatic IGF-I mRNA expression in coho salmon were examined in vivo. Liver had the highest IGF-I mRNA level of 16 pg/μg DNA. Significant amounts of IGF-I mRNA were also found in all other tissues examined (intestine 4.1, kidney 3.8, gill arch 2.4, brain 2.4, ovary 2.3, muscle 2.1, spleen 1.7 and fat 1.1 pg/μg DNA). Injection of coho salmon GH at doses of 0.1 and 1 μg/g body weight significantly increased the hepatic IGF-I mRNA levels in a dose-dependent manner. Injection of coho salmon SL, a recently discovered member of the GH/PRL family, stimulated the IGF-I mRNA expression at the higher dose (1 μg/g), whereas coho salmon PRL had no effect at either dose. Concentration-dependent stimulation by coho salmon GH was also obtained in vitro in primary culture of salmon hepatocytes in concentrations ranging from 0.01 to 1 μg/ml. These results indicate that IGF-I mRNA expression occurs in a variety of tissues in coho salmon, and that at least the hepatic expression is under the regulation of GH and possibly other hormones. The sequence-specific assay established in the present study can be used for accurate quantitation of IGF-I mRNA in salmonid species, and can contribute to a better understanding of the physiology of IGF-I in salmonids.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Fish physiology and biochemistry 9 (1991), S. 351-360 
    ISSN: 1573-5168
    Keywords: Trout (Oncorhynchus mykiss) ; skeletal muscles ; insulin binding ; carbohydrate diet
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two hundred rainbow trout (Oncorhynchus mykiss) age 0 +, weight range 11.3 – 11.5 g, were distributed randomly in two groups and maintained for five weeks on either 10% dextrin, or 20% dextrin diet. The fish were sampled 3–5 h and 18–20 h after the last feeding and insulin binding to partially purified insulin receptors in white and red skeletal muscles and to liver plasma membranes was assessed. Plasma insulin, plasma glucose, and liver glycogen content were analyzed in the same fish. Fish fed a diet with higher carbohydrate content (HC) had elevated insulin and glucose levels in peripheral blood, but lower liver glycogen contents compared to the fish fed a diet with lower carbohydrate content (LC). No growth retardation was observed in the fish from HC group. Three to five hours after the last feeding, insulin-receptor binding in white skeletal muscles was higher in HC group of fish, mostly because of an increase in number of high affinity binding sites. Eighteen to twenty hours after the last feeding this difference disappeared. In contrast, the specific binding of insulin to the liver plasma membranes appeared to be lower in the HC group of fish. The lower insulin binding to the liver plasma membranes observed 3–5 h after feeding, could be attributed to the lower quantity of binding sites, while the same phenomenon 18 h after feeding was likely a result of affinity changes. We conclude that higher glycemic levels observed in trout fed a HC diet as compared to LC group of fish, are not a consequence of impaired binding of insulin to its receptors in skeletal muscles.
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  • 6
    ISSN: 1573-5168
    Keywords: hepatocytes ; salmonids ; insulin binding ; insulin processing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Résumé Ce travail devait nous permettre de savoir si: 1) de l'insuline ajoutée à du milieu d'incubation d'hépatocytes isolés de saumon atlantique (Salmo salar) et de truite arc-en-ciel (Oncorhynchus mykiss) était capable de contrôler négativement le nombre de récepteurs à l'insuline; 2) une évaluation différentielle quantitative du devenir de l'insuline était possible sur des cellules hépatiques isolées de poisson; 3) la température pouvait affecter la liaison à l'insuline et contrôler négativement le nombre de récepteurs à l'insuline. Après leur individualisation et une courte “période de régénération métabolique”, des cellules hépatiques ont été utilisées pour des études de liaison avec de l'125I insuline, directement ou après une préincubation (18h à 4°C ou 3h à 15°C) en présence d'insuline mammalienne ou de saumon (1 à 1000 nM). Une préincubation à 15°C diminue la capacité de liaison (nombre de sites de liaison par cellule hépatique) de toutes les preparations d'hépatocytes traitées avec 1000 nM d'insuline, et dans 4 des 5 préparations traitées avec 100 nM d'insuline. A 4°C, les sites de liaison de l'insuline ne sont régulés négativement que dans moins de 50% des préparations hépatocytaires et seulement en présence de 1000 nM d'insuline. Une évaluation différentielle quantitative a été effectuée sur a) l'insuline libre intact; b) l'insuline dégradée; c) l'insuline liée intact; d) l'insuline internalisée mais dégradée, et e) l'insuline intacte internalisée par les cellules hépatiques. Des hépatocytes préincubés à 15°C en présence de 100–1000 nM d'insuline, lient et internalisent moins l'125I insuline. Nous émettons l'hypothèse que, in vivo, à des températures égales ou supérieures à 15°C, des niveaux extrêmes mais physiologiques d'insuline sont capables de réguler le nombre de récepteurs de l'insuline dans le foie des salmonidés. Inversement, chez les poissons vivant en eau froide, la régulation des récepteurs à l'insuline, par l'insuline plasmatique, a un faible rôle physiologique.
    Notes: Abstract The questions addressed in this study were: 1) whether insulin added to the incubation medium can down-regulate 125I insulin binding to isolated hepatocytes of Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss); 2) whether quantitative assessment of insulin processing can be made on isolated fish liver cells; 3) how ambient temperatures can affect insulin binding, and down-regulation of insulin receptors. After isolation and a short (up to 4h) “metabolic recovery period”, liver cells were used either directly in 125I insulin binding assay or first preincubated for 18h at 4°C or for 3h at 15°C, with or without mammalian or salmon insulin in concentrations ranging from 1 to 1000 nM. Preincubation at 15°C, decreased binding capacity (number of binding sites per liver cell) in all five independent hepatocyte preparations treated with 1000 nM insulin and in four out of five preparations treated with 100 nM insulin. At 4°C insulin binding sites were down-regulated in less than 50% of all hepatocyte preparations and only in the presence of 1000 nM insulin. Differential quantitive assessment was made of a) intact free insulin; b) insulin degraded; c) intact insulin bound to the cell membrane; d) internalized but degraded insulin, and e) intact insulin internalized by liver cells. Hepatocytes preincubated with 100 – 1000 nM insulin at 15°C bound and internalized less 125I insulin. We hypothesize that in vivo, at water temperatures of 15°C and higher, extreme physiological levels of plasma insulin may regulate the numbers of insulin receptors in the salmonid liver. In contrast, in fish inhabiting cold waters the regulation of insulin receptors by circulating plasma insulin seems to be of little physiological importance.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Fish physiology and biochemistry 11 (1993), S. 429-438 
    ISSN: 1573-5168
    Keywords: amphibians ; cAMP ; evolution ; GLP ; glucagon ; mammals ; message transduction ; pancreas ; receptor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Abstract In amphibians and mammals, the preproglucagon gene encodes two related GLPs - GLP-1(37 residues) and GLP-2 (34 residues). The physiologically functional GLPs, however, are GLP-17−36amide, or similar, truncated forms of GLP-1. While the liver is devoid of GLP receptors and fails to respond metabolically, brain, gastric cells and pancreatic cells have been identified as potential target sites. These tissues possess specific binding sites for truncated GLP-1, and generally, cells respond to truncated GLPs with increases in CAMP. In mammalian pancreas, truncated GLPs function as powerful insulinotropins, while also increasing insulin gene transcription and inhibiting glucagon release. Full length GLP-1 is a weak insulinotropin only. To date, neither metabolic nor endocrine actions have been assigned to GLP-2. Following processing of preproglucagon gene products, fish pancreas and intestine contain only one GLP (31 residues) displaying considerable sequence homology with GLP-17−36. Applied in low nanomolar concentrations, fish GLPs, together with GLP-17−36, activate hepatic glycogenolysis, gluconeogenesis and lipolysis in fishes. Thousand-fold higher levels of GLP-17−37 are required to elicit comparable metabolic effects. Generally, the metabolic actions of GLPs are similar to those for glucagon, but GLPs tend to be more potent in their specific actions. Fish livers possibly contain GLP receptors distinct from glucagon receptors. Message transduction in some, but not all fish species, may involve adenylyl cyclase and CAMP, but correlation between metabolic activation and cAMP levels is generally poor. Fish GLP seems to be a very weak insulinotropin in Brockmann bodies.
    Notes: Résumé Chez les amphibians et les mammifères, le gène du préproglucagon code pour deux GLP voisins — GLP-1 (37 résidues) et GLP-2 (34 résidues). Cependant, les GLP physiologiquement fonctionnels sont l'amide de GLP-17−36 ou des formes similaires trongées de GLP-1. Alors que le foie est dépourvu de récepteurs à GLP et ne répond pas sur le plan métabolique, le cerveau, les cellules gastriques et les cellules pancréatiques ont été identifiés comme étant des cibles potentielles. Ces tissues possèdent des sites de liaison spécifiques pour le GLP tronqué et, en général, les cellules répondent aux GLP tronqués en augmentant leur AMPc. Dans le pancréas de mammifères, les GLP tronqués agissent comme des insulinotropines puissantes, en augmentant la transcription du gène insuline et en inhibitant la libération de glucagon. Le GLP-1 entier est une insulinotropine faible. Actuellement, aucune action métabolique ou endocrine n'a été trouvée pour le GLP-2. Si l'on suit la mise en place des produits du gène préproglucagon, le pancréas et l'intestin de poisson ne contiennent qu'un seul GLP (31 résidues) qui présente des homologies de séquence considérables avec le GLP-17−36. Appliqués à des concentrations de l'ordre du nanomolaire, les GLPs de poisson, de même que le GLP-17−36, activent la glyconéogénèse et la lipolyse chez les poissons. Des doses mille fois plus élevés de GLP-11−37 sont nécessaires pour obtenir des effets métaboliques comparables. En général, les effets métaboliques des GLP sont identiques à ceux du glucagon, mais les GLP à être plus actifs dans leurs effets spécifiques. Les foies de poissons pourraient contenir des récepteurs au GLP différents des récepteurs au glucagon. La transduction du message chez certaines espèces de poission mais pas toutes, pourraient faire intervenir l'adénylyl cyclase et l'AMPc, mais la corrélation entre l'activité métabolique et les niveaux d'AMPc reste en général faible. Dans les corps de Brockmann, le GLP de poisson semble agir comme une insulinotropine très peu active.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fish physiology and biochemistry 9 (1991), S. 223-230 
    ISSN: 1573-5168
    Keywords: salmonids ; body weight ; radioimmunoassays ; insulin ; glucagon ; glucagon-like peptide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plasma levels of insulin in rainbow trout,Oncorhynchus mykiss, Atlantic salmon,Salmo salar, and Pacific coho salmon,Oncorhynchus kisutch and plasma circulating levels of glucagon and glucagon-like peptide, in rainbow trout and Atlantic salmon, were measured by homologous radioimmunoassays. Hormonal levels were compared against the average body weight of the same group of fish. Plasma insulin levels were significantly correlated (r=0.56, 0.46 and 0.42 respectively) with body weight in all three salmonid species. Moreover, rainbow trout from fast-growing families had significantly higher (p〈0.005) plasma insulin levels than did fish from slow-growing families. Plasma titres of glucagon and glucagon-like peptide were always lower than insulin titres and did not correlate with body weight.
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  • 9
    ISSN: 1573-5168
    Keywords: insulin ; glycogen ; Atlantic salmon ; smoltification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plasma levels of insulin were measured by specific radioimmunoassay in 1-year and 2-year old Atlantic salmon (Salmo salar) parr during the period of parr-smolt transformation. The two-year old fish were of two different categories; silvering pre-smolts and previously mature male parr. If insulin plays an important role in parr-smolt transformation and/or subsequent osmoregulatory changes it was expected that the pre-smolts would show a different insulin profile compared to the mature male parr and one-year old parr, both of which show impaired hypoosmoregulatory ability compared to smolts. Measurements were taken during two separate years. Between January and April both categories of two-year old fish had generally higher plasma levels of insulin compared to the non-smolting one-year old parr. In the pre-smolts insulin levels ranged from 4.0 to 7.9 ng ml−1, and from 7.8 to 16.7 ng ml−1 in 1990 and 1992 respectively, while in the previously mature males the same respective values were from 4.3 to 10.0 ng ml−1, and from 6.6 to 24.1 ng ml−1. In the two-year old fish, whether pre-smolts or mature males, plasma insulin levels peaked between 1–2 months before final smoltification, after which insulin titers declined sharply. In 1990, the 1-year old parr showed a dual peak in plasma insulin. Insulin first peaked in February (7.8 ng ml−1), and then again in April–May (7.7 ng ml−1), while in 1992 the 1-year old parr showed a number of smaller transient peaks (5–7 ng ml−1) between March–May, followed by sharp elevation of insulin levels in June. Liver glycogen contents were at their highest (3.5–5.0 g 100 g−1 I liver wet weight) in March in both 1-year and 2-year old fish. Glycogen levels were low during the later stages of parr-smolt transformation, before rising again in June in both the 1-year old and precociously mature parr, but not in the smolts.
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  • 10
    ISSN: 1573-5168
    Keywords: reproductive cycle ; metabolism ; estrogen ; vitellogenin ; insulin ; thyroid hormones ; salmon ; ovulation ; gonadotropin ; eggs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Circulating concentrations of estradiol (E2), vitellogenin (VTG), thyroxine (T4), triiodothyronine (T3) and insulin were measured in reproductively maturing four and five year-old Atlantic salmon. Blood samples were collected from the fish in seawater for one year prior to their spawning in November in fresh water. In females, E2 and VTG were low but detectable from December to July, and then increased to peak levels in September and October. Plasma levels of T4 and T3 were relatively constant in winter and spring, and decreased in July. Plasma concentration of T4 increased in November when the fish returned to fresh water. Plasma T3 levels remained low during the autumn. Both T4 and T3 levels tended to be higher in males than in females during September through November. Plasma insulin concentrations increased during the spring to peak values in May, and then decreased in June and July in fish of both sexes. There was a significant elevation of plasma insulin in males during October, and the levels in males tended to be higher than those found in females during final maturation.
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