Literature DB >> 24221753

Physiology of fish endocrine pancreas.

E M Plisetskaya1.   

Abstract

From the very beginning of physiological studies on the endocine pancreas, fish have been used as experimental subjects. Fish insulin was one of the first vertebrate insulins isolated and one of the first insulins whose primary and then tertiary structures were reported. Before a second pancreatic hormone, glucagon, was characterized, a physiologically active 'impurity', similar to that in mammalian insulin preparations, was found in fish insulins.Fish have become the most widely used model for studies of biosynthesis and processing of the pancreatic hormones. It seems inconceivable, therefore, that until the recent past cod and tuna insulins have been the only purified piscine islet hormones available for physiological experiments. The situation has changed remarkably during the last decade.In this review the contemporary status of physiological studies on the fish pancreas is outlined with an emphasis on the following topics: 1) contents of pancreatic peptides in plasma and in islet tissue; 2) actions of piscine pancreatic hormones in fish; 3) specific metabolic consequences of an acute insufficiency of pancreatic peptides; 4) functional interrelations among pancreatic peptides which differ from those of mammals. The pitfalls, lacunae and the perspectives of contemporary physiological studies on fish endocrine pancreas are outlined.

Entities:  

Year:  1989        PMID: 24221753     DOI: 10.1007/BF00004688

Source DB:  PubMed          Journal:  Fish Physiol Biochem        ISSN: 0920-1742            Impact factor:   2.794


  43 in total

1.  The content of glycogenolytic factor in pancreas from different species.

Authors:  G AUDY; M KERLY
Journal:  Biochem J       Date:  1952-09       Impact factor: 3.857

Review 2.  The biosynthesis of C14- and H3- labeled insulin.

Authors:  G E Bauer; A W Lindall; A Lazarow
Journal:  Adv Tracer Methodol       Date:  1965

3.  Separate cell types that express two different forms of somatostatin in anglerfish islets can be immunohistochemically differentiated.

Authors:  J K McDonald; F Greiner; G E Bauer; R P Elde; B D Noe
Journal:  J Histochem Cytochem       Date:  1987-02       Impact factor: 2.479

4.  [Insulin receptor reaction of the lamprey Lampetra fluvialis to hyperinsulinemia induced by administration of the hormone].

Authors:  B N Leĭbush; L P Soltitskaia; M V Ukhanova
Journal:  Zh Evol Biokhim Fiziol       Date:  1987 Jul-Aug

5.  Colocalization of glucagon-like peptide and glucagon immunoreactivities in pancreatic islets and intestine of salmonids.

Authors:  M Nozaki; K Miyata; Y Oota; A Gorbman; E M Plisetskaya
Journal:  Cell Tissue Res       Date:  1988-08       Impact factor: 5.249

6.  Glucagon-like peptides activate hepatic gluconeogenesis.

Authors:  T P Mommsen; P C Andrews; E M Plisetskaya
Journal:  FEBS Lett       Date:  1987-07-13       Impact factor: 4.124

7.  Immunocytochemical localization of hormone-producing cells within the pancreatic islets of the rainbow trout (Salmo gairdneri).

Authors:  G F Wagner; B A McKeown
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

8.  Anglerfish preprosomatostatin II is processed to somatostatin-28 and contains hydroxylysine at residue 23.

Authors:  P C Andrews; D Hawke; J E Shively; J E Dixon
Journal:  J Biol Chem       Date:  1984-12-25       Impact factor: 5.157

9.  Different cellular distributions of two somatostatins in brain and pancreas of salmonids, and their associations with insulin- and glucagon-secreting cells.

Authors:  M Nozaki; K Miyata; Y Oota; A Gorbman; E M Plisetskaya
Journal:  Gen Comp Endocrinol       Date:  1988-02       Impact factor: 2.822

10.  Pancreatic and thyroid hormones in rainbow trout (Salmo gairdneri): what concentration does the liver see?

Authors:  E M Plisetskaya; C V Sullivan
Journal:  Gen Comp Endocrinol       Date:  1989-08       Impact factor: 2.822

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  6 in total

1.  Dietary carbohydrate utilization in cod (Gadus morhua): metabolic responses to feeding and fasting.

Authors:  G I Hemre; O Lie; A Sundby
Journal:  Fish Physiol Biochem       Date:  1993-04       Impact factor: 2.794

Review 2.  Glucose metabolism in fish: a review.

Authors:  Sergio Polakof; Stéphane Panserat; José L Soengas; Thomas W Moon
Journal:  J Comp Physiol B       Date:  2012-04-05       Impact factor: 2.200

3.  Histological changes in insulin-immunoreactive pancreatic β-cells, and suppression of insulin secretion and somatotrope activity in brook trout (Salvelinus fontinalis) maintained on reduced food intake or exposed to acidic environment.

Authors:  D B Mackett; W H Tam; J N Fryer
Journal:  Fish Physiol Biochem       Date:  1992-10       Impact factor: 2.794

4.  Utilization of dietary starch and glucose tolerance in juvenile chinook salmon (Oncorhynchus tshawytscha) of different strains in seawater.

Authors:  C N Mazur; D A Higgs; E Plisetskaya; B E March
Journal:  Fish Physiol Biochem       Date:  1992-12       Impact factor: 2.794

Review 5.  Pesticide Pollution: Detrimental Outcomes and Possible Mechanisms of Fish Exposure to Common Organophosphates and Triazines.

Authors:  Ihab Khatib; Piotr Rychter; Halina Falfushynska
Journal:  J Xenobiot       Date:  2022-09-02

Review 6.  MicroRNA in teleost fish.

Authors:  Teshome Tilahun Bizuayehu; Igor Babiak
Journal:  Genome Biol Evol       Date:  2014-07-22       Impact factor: 3.416

  6 in total

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