Literature DB >> 15447686

A stereological evaluation of secretin and gastric inhibitory peptide-containing mucosal cells of the perinatal small intestine of the pig.

C Van Ginneken1, A Weyns.   

Abstract

Stereological methods were used to quantify secretin and gastric inhibitory peptide (GIP)-immunoreactivity (GIP-IR) in paraffin sections of the duodenum, jejunum and ileum of fetal and neonatal piglets. In addition, sections were processed for GLP-1-immunohistochemistry. The volume density of the tunica mucosa increased after birth, giving rise to a decreased volume density of the tela submucosa and tunica muscularis. Generally known region-specific morphological distinctions were reflected in differing volume densities of the various layers. The highest volume density of GIP-IR epithelial cells was observed in the jejunum of the neonate. In contrast, the volume density of secretin-IR epithelial cells was highest in the duodenum of both fetal and neonatal piglets. The volume occupied by GIP-IR and secretin-IR epithelial cells increased in the jejunum after birth. Additionally, ileal secretin-IR epithelial cells were more numerous in the neonatal piglet. In conclusion, the quantitative and qualitative presence of GIP-IR and secretin-IR epithelial cells agree with earlier reports of their presence and co-localization between GIP-IR and GLP-1-IR, in the pig small intestine. Furthermore, the differences suggest that age- and region-related functional demands are temporally and probably causally related with the morphological diversification of the intestine and its endocrine cells.

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Year:  2004        PMID: 15447686      PMCID: PMC1571350          DOI: 10.1111/j.0021-8782.2004.00338.x

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  38 in total

1.  Colocalization of GLP-1 and GIP in human and porcine intestine.

Authors:  K Mortensen; L L Petersen; C Ørskov
Journal:  Ann N Y Acad Sci       Date:  2000       Impact factor: 5.691

Review 2.  The metabolic role of GIP: physiology and pathology.

Authors:  L M Morgan
Journal:  Biochem Soc Trans       Date:  1996-05       Impact factor: 5.407

3.  Plasma and intestinal concentrations of GIP and GLP-1 (7-36) amide during suckling and after weaning in pigs.

Authors:  J M Knapper; L M Morgan; J M Fletcher; V Marks
Journal:  Horm Metab Res       Date:  1995-11       Impact factor: 2.936

4.  Complex co-localization of chromogranins and neurohormones in the human gastrointestinal tract.

Authors:  G M Portela-Gomes; M Stridsberg; H Johansson; L Grimelius
Journal:  J Histochem Cytochem       Date:  1997-06       Impact factor: 2.479

Review 5.  Key nutrients and growth factors for the neonatal gastrointestinal tract.

Authors:  Douglas G Burrin; Barbara Stoll
Journal:  Clin Perinatol       Date:  2002-03       Impact factor: 3.430

6.  Postnatal development of intestinal endocrine cell populations in the water buffalo.

Authors:  C Lucini; P De Girolamo; L Coppola; G Paino; L Castaldo
Journal:  J Anat       Date:  1999-10       Impact factor: 2.610

7.  Small intestinal disaccharidase activity and ileal villus height are increased in piglets consuming formula containing recombinant human insulin-like growth factor-I.

Authors:  V M Houle; E A Schroeder; J Odle; S M Donovan
Journal:  Pediatr Res       Date:  1997-07       Impact factor: 3.756

8.  Stereologic characteristics of pig small intestine during normal development.

Authors:  C Van Ginneken; F Van Meir; A Weyns
Journal:  Dig Dis Sci       Date:  2002-04       Impact factor: 3.199

9.  Stereologic evaluation of the pig gastric wall and of somatostatinergic and serotoninergic immunoreactive mucosal cells during perinatal development.

Authors:  C van Ginneken; A Weyns; E van Meir
Journal:  Eur J Morphol       Date:  2001-04

10.  How age changes the content of neuroendocrine peptides in the murine gastrointestinal tract.

Authors:  M El-Salhy; O Sandström
Journal:  Gerontology       Date:  1999 Jan-Feb       Impact factor: 5.140

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  1 in total

1.  Pancreatic glucose-dependent insulinotropic polypeptide (GIP) (1-30) expression is upregulated in diabetes and PEGylated GIP(1-30) can suppress the progression of low-dose-STZ-induced hyperglycaemia in mice.

Authors:  Tsuyoshi Yanagimachi; Yukihiro Fujita; Yasutaka Takeda; Jun Honjo; Kuralay K Atageldiyeva; Yumi Takiyama; Atsuko Abiko; Yuichi Makino; Timothy J Kieffer; Masakazu Haneda
Journal:  Diabetologia       Date:  2015-12-22       Impact factor: 10.122

  1 in total

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