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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1994-9-8
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pubmed:abstractText |
Rat bladder hypertrophy, induced by a partial ligation of the urethra, was used to study the accompanying changes of microvascular smooth muscle mechanics, pharmacology and morphology. A segment of a microarterial vessel to the bladder was taken from a defined anatomical location and studied in a wire myograph in vitro at the length for maximal isometric force development (Lmax). After 10 days of ligation, bladder hypertrophy resulted in a microvascular growth response compared to non-operated controls which was characterized by (i) an increase of the calculated diameter at Lmax from 134 +/- 5 microns to 222 +/- 19 microns; (ii) an increase of the media thickness from 22.4 +/- 1.9 microns to 32.2 +2- 3.0 microns; (iii) an increase of the active tension from 1.42 +/- 0.28 mN/mm to 3.06 +/- 0.33 mN/mm; (iv) no change of the wall/lumen ratio (from 0.83 +/- 0.10 to 0.79 +/- 0.15). Normalized length/force relations (active, passive and total) did not differ significantly between microarteries from control and hypertrophic bladders. Microvascular smooth muscle growth was also associated with a decreased sensitivity to K(+)-induced depolarization and an increased sensitivity to alpha 1-adrenergic stimulation. No differences were noted regarding the Ca2+ sensitivity of force during K(+)-induced depolarization. The results suggest that microvascular growth (1) is immediately and positively influenced by the organ growth; (2) results in a functional resetting of the microvascular segments towards larger diameters without gross morphological or mechanical alterations; and (3) is accompanied by pharmacological alterations of the smooth muscle reactivity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0031-6768
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
426
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
506-15
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8052520-Animals,
pubmed-meshheading:8052520-Arterioles,
pubmed-meshheading:8052520-Carbachol,
pubmed-meshheading:8052520-Female,
pubmed-meshheading:8052520-Histocytochemistry,
pubmed-meshheading:8052520-Hypertrophy,
pubmed-meshheading:8052520-Microscopy, Electron,
pubmed-meshheading:8052520-Muscle, Smooth, Vascular,
pubmed-meshheading:8052520-Muscle Contraction,
pubmed-meshheading:8052520-Muscle Development,
pubmed-meshheading:8052520-Phenylephrine,
pubmed-meshheading:8052520-Potassium,
pubmed-meshheading:8052520-Rats,
pubmed-meshheading:8052520-Rats, Sprague-Dawley,
pubmed-meshheading:8052520-Regional Blood Flow,
pubmed-meshheading:8052520-Urinary Bladder,
pubmed-meshheading:8052520-Urinary Bladder Diseases
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pubmed:year |
1994
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pubmed:articleTitle |
Structure and mechanics of growing arterial microvessels from hypertrophied urinary bladder in the rat.
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pubmed:affiliation |
Department of Physiology and Biophysics, Lund University, Sweden.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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