Literature DB >> 508951

Adult microvascular disturbances as a result of juvenile onset diabetes in Db/Db mice.

H G Bohlen, B A Niggl.   

Abstract

The arterioles in the cremaster muscle of 8 to 10-week-old Ob/Ob, Db/Db and stroptozotocin diabetic mice are characterized by a decreased number of arterioles, loss of vascular tone and a reduced cross-sectional area of the vessel walls. The present study was designed to determine if these abnormalities persist to adult life or if additional abnormalities develop to cause vascular dysfunction. The diameters, wall thickness to lumen ratios and vessel wall areas of comparable types of innervated arterioles in 24- to 28-week-old normal and Db/Db mice are equivalent, except that the smallest arterioles of Db/Db have thin vessel walls. However, blood flow at rest is only 3.0 +/- 0.9 ml/min/100 g of cremasteric muscle tissue in Db/Db mice as compared to 5.5 +/- 1.3 ml/min/100 g in normal mice. After all vascular control is abolished, the arterioles of Db/Db dilated, but significantly (p less than 0.05) less than in normal animals. The minimum distance between adjacent capillaries (wall to wall) during the passive state was 28 +/- 1.7 micron in Db/Db mice and 21.8 +/- 0.6 micron in normal mice; this indicates a major decrease of vascularity in the adult Db/Db mouse. The results obtained indicate that the reduction in numbers of arterioles and loss of vascular tone in juvenile diabetic mice persists to adult life but arteriolar wall characteristics become normal in adult life.

Entities:  

Mesh:

Year:  1979        PMID: 508951     DOI: 10.1159/000158215

Source DB:  PubMed          Journal:  Blood Vessels        ISSN: 0303-6847


  13 in total

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2.  Renal vessel changes in diabetic KK-mice.

Authors:  H P Volkmann; H Wehner
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Review 3.  Fibrinogen-Related Proteins in Tissue Repair: How a Unique Domain with a Common Structure Controls Diverse Aspects of Wound Healing.

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4.  Adeno-associated viral vector-mediated human vascular endothelial growth factor gene transfer stimulates angiogenesis and wound healing in the genetically diabetic mouse.

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5.  Early arteriolar and capillary changes in streptozotocin-induced diabetic rats and intraperitoneal hyperglycaemic rats.

Authors:  H G Bohlen; K D Hankins
Journal:  Diabetologia       Date:  1982-05       Impact factor: 10.122

6.  Transgenic overexpression of keratinocyte-specific VEGF and Ang1 in combination promotes wound healing under nondiabetic but not diabetic conditions.

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7.  Terminal arteriolar network structure/function and plasma cytokine levels in db/db and ob/ob mouse skeletal muscle.

Authors:  Melissa K Georgi; Jacqueline Vigilance; Anthony M Dewar; Mary D Frame
Journal:  Microcirculation       Date:  2011-04       Impact factor: 2.628

8.  Inhibition of inflammasome activation improves the impaired pattern of healing in genetically diabetic mice.

Authors:  Alessandra Bitto; Domenica Altavilla; Gabriele Pizzino; Natasha Irrera; Giovanni Pallio; Michele R Colonna; Francesco Squadrito
Journal:  Br J Pharmacol       Date:  2014-05       Impact factor: 8.739

9.  Morphometric investigations on intrarenal vessels of streptozotocin-diabetic rats.

Authors:  H Wehner; G Nelischer
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

10.  Decreased macrophage number and activation lead to reduced lymphatic vessel formation and contribute to impaired diabetic wound healing.

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Journal:  Am J Pathol       Date:  2007-04       Impact factor: 4.307

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