Literature DB >> 499075

Phylogenetic and anatomical distribution of somatostatin in vertebrates.

J A King, R P Millar.   

Abstract

Immunoreactive GH release-inhibiting factor [somatostatin (SRIF)] was detected in hypothalamus, extrahypothalamic brain, pancreas, and stomach extracts of the rat, pigeon, tortoise, frog, teleost (cichlid), and elasmobranch (dogfish) and in the whole brain of the cyclostome (hagfish). The SRIF concentration was higher in the pancreas and gastrointestinal tract than in the hypothalamus and extrahypothalamic brain in most species. Extracts of the various tissues from the different species assayed in serial dilutions gave displacement curves parallel to those of synthetic mammalian SRIF. Cation exchange chromatography of hypothalamic extracts from the various species revealed two major immunoreactive peaks, one of which correpsonds to synthetic SRIF in elution volume, the other being less basic. Affinity chromatography-purified immunoreactive SRIF from frog brain, pancreas, and stomach extracts coeluted with synthetic SRIF in high pressure liquid chromatography. The results indicate that immunoreactive SRIF in various tissues and in different vertebrates is indistinguishable and suggest that there has been no change in the molecule during at least 400 million yr of evolution.

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Year:  1979        PMID: 499075     DOI: 10.1210/endo-105-6-1322

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  9 in total

1.  Immunocytochemical and ultrastructural characterization of endocrine cells in chicken proventriculus.

Authors:  A Martínez; J López; M A Barrenechea; P Sesma
Journal:  Cell Tissue Res       Date:  1991-03       Impact factor: 5.249

2.  Ultrastructural studies of endocrine-like cells in the fundic gastric mucosa of the bullfrog, Rana catesbeiana.

Authors:  F Michelangeli; D M Sulcas; M C Ruiz
Journal:  Cell Tissue Res       Date:  1987-11       Impact factor: 5.249

3.  Somatostatin in the brain and the pituitary of some teleosts. Immunocytochemical identification and the effect of starvation.

Authors:  M Olivereau; F Ollevier; F Vandesande; J Olivereau
Journal:  Cell Tissue Res       Date:  1984       Impact factor: 5.249

4.  Immunocytochemical evidence for the presence of somatostatin-like immunoreactivity in scattered cells of the duct system of the submandibular glands in the monkey, Macaca irus.

Authors:  C Girod; M P Dubois; N Durand
Journal:  Histochemistry       Date:  1980

5.  Relationship between urotensin II- and somatostatin-immunoreactive spinal cord neurons of Catostomus commersoni and Oncorhynchus kisutch (Teleostei).

Authors:  C R Yulis; K Lederis
Journal:  Cell Tissue Res       Date:  1988       Impact factor: 5.249

6.  Hypothalamic lesions stimulating growth hormone cell activity in the goldfish.

Authors:  J N Fryer
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

7.  Antisomatostatin-induced growth acceleration in chinook salmon (Oncorhynchus tshawytscha).

Authors:  I Mayer; E McLean; T J Kieffer; L M Souza; E M Donaldson
Journal:  Fish Physiol Biochem       Date:  1994-10       Impact factor: 2.794

8.  Immunocytochemical localization of somatostatin and vasotocin in the brain of the Pacific hagfish, Eptatretus stouti.

Authors:  M Nozaki; A Gorbman
Journal:  Cell Tissue Res       Date:  1983       Impact factor: 5.249

9.  Ontogeny of somatostatin-immunoreactive systems in the brain of the brown trout (Teleostei).

Authors:  M Becerra; M J Manso; I Rodríguez-Moldes; R Anadón
Journal:  Anat Embryol (Berl)       Date:  1995-02
  9 in total

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