Literature DB >> 8155905

Morphological effects of diabetes on the granular ducts and acini of the rat submandibular gland.

L C Anderson1, A H Suleiman, J R Garrett.   

Abstract

Effects of experimental diabetes on rat submandibular glands have been documented, but earlier reports suggested that diabetes caused an extensive cellular degeneration and a replacement of the parenchymal cells by fibrous connective tissue. Such observations, however, are difficult to reconcile with the relatively normal physiological responsiveness of the gland (Anderson and Suleiman, 1989). This study, therefore, reexamined the histological, histochemical and ultrastructural effects of streptozotocin-induced diabetes on rat submandibular glands. The tissues were examined at 3 weeks, and 3 and 6 months after the induction of diabetes, and compared with glands from age-matched controls by both light and electron microscopy. Light microscopically, the proportional volumes of the acini and granular ducts remained constant in control rats at about 48% and 38% respectively. In diabetic animals the volume density of the acini increased progressively to 62%, whereas that of the granular ducts decreased to 20%. The diameter and number of granular ducts were reduced in diabetic animals, but acinar cell profile area was only affected 6 months after the induction of diabetes. Ultrastructurally, there was an accumulation of lipid in the acinar cells and, with increasing duration of diabetes, the number of autophagic structures in both the acini and the granular ducts increased. Although there was evidence of some cellular degeneration it was never excessive. Morphometry showed that the volume density of secretory granules within the acinar cells was unaffected, but there was a significant reduction in the volume density of secretory granules within the granular ducts. Thus, in the rat submandibular gland the greatest effect of streptozotocin-induced diabetes was to cause hypotrophic changes in the cells of the granular ducts. The relative contributions of a direct effect of insulin insufficiency and the hypogonadal effects of diabetes, however, are not known.

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Year:  1994        PMID: 8155905     DOI: 10.1002/jemt.1070270105

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  7 in total

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2.  Influence of streptozotocin-induced diabetes on hexokinase activity of rat salivary glands.

Authors:  F N Nogueira; M F dos Santos; J Nicolau
Journal:  J Physiol Biochem       Date:  2005-09       Impact factor: 4.158

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Journal:  Eurasian J Med       Date:  2015-10

4.  Insulin Resistance and Obesity Affect Lipid Profile in the Salivary Glands.

Authors:  Jan Matczuk; Anna Zalewska; Bartłomiej Łukaszuk; Małgorzata Knaś; Mateusz Maciejczyk; Marta Garbowska; Dominika M Ziembicka; Danuta Waszkiel; Adrian Chabowski; Małgorzata Żendzian-Piotrowska; Krzysztof Kurek
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Journal:  J Cell Physiol       Date:  2017-04-27       Impact factor: 6.384

6.  Larrea divaricata Cav. aqueous extract and nordihydroguariaretic acid modulate oxidative stress in submandibular glands of diabetic rats: a buccal protective in diabetes.

Authors:  Ignacio Peralta; Carla Marrassini; María Laura Barreiro Arcos; Graciela Cremaschi; María Rosario Alonso; Claudia Anesini
Journal:  BMC Complement Altern Med       Date:  2019-08-22       Impact factor: 3.659

7.  Disruption of tight junctions contributes to hyposalivation of salivary glands in a mouse model of type 2 diabetes.

Authors:  Yan Huang; Qian-Ying Mao; Xi-Jin Shi; Xin Cong; Yan Zhang; Li-Ling Wu; Guang-Yan Yu; Ruo-Lan Xiang
Journal:  J Anat       Date:  2020-05-06       Impact factor: 2.921

  7 in total

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