Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries
<p>Abstract</p> <p>Background</p> <p>Poor control of blood glucose in diabetes is known to promote vascular dysfunction and hypertension. Diabetes was recently shown to be linked to an increased prevalence of pulmonary hypertension. The aim of this study was to determin...
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| Format: | Article |
| Language: | English |
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BMC
2009-01-01
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| Series: | Cardiovascular Diabetology |
| Online Access: | http://www.cardiab.com/content/8/1/4 |
| _version_ | 1811247081414721536 |
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| author | Howarth Frank C Gurney Alison M |
| author_facet | Howarth Frank C Gurney Alison M |
| author_sort | Howarth Frank C |
| collection | DOAJ |
| description | <p>Abstract</p> <p>Background</p> <p>Poor control of blood glucose in diabetes is known to promote vascular dysfunction and hypertension. Diabetes was recently shown to be linked to an increased prevalence of pulmonary hypertension. The aim of this study was to determine how the pharmacological reactivity of intrapulmonary arteries is altered in a rat model of diabetes.</p> <p>Methods</p> <p>Diabetes was induced in rats by the β-cell toxin, streptozotocin (STZ, 60 mg/kg), and isolated conduit and resistance intrapulmonary arteries studied 3–4 months later. Isometric tension responses to the vasoconstrictors phenylephrine, serotonin and PGF<sub>2α</sub>, and the vasodilators carbachol and glyceryl trinitrate, were compared in STZ-treated rats and age-matched controls.</p> <p>Results</p> <p>STZ-induced diabetes significantly blunted the maximum response of conduit, but not resistance pulmonary arteries to phenylephrine and serotonin, without a change in pEC<sub>50</sub>. Agonist responses were differentially reduced, with serotonin (46% smaller) affected more than phenylephrine (32% smaller) and responses to PGF<sub>2α </sub>unaltered. Vasoconstriction caused by K<sup>+</sup>-induced depolarisation remained normal in diabetic rats. Endothelium-dependent dilation to carbachol and endothelium-independent dilation to glyceryl trinitrate were also unaffected.</p> <p>Conclusion</p> <p>The small resistance pulmonary arteries are relatively resistant to STZ-induced diabetes. The impaired constrictor responsiveness of conduit vessels was agonist dependent, suggesting possible loss of receptor expression or function. The observed effects cannot account for pulmonary hypertension in diabetes, rather the impaired reactivity to vasoconstrictors would counteract the development of pulmonary hypertensive disease.</p> |
| first_indexed | 2024-04-12T15:03:10Z |
| format | Article |
| id | doaj.art-49bc82389291461194d945532af0a5e8 |
| institution | Directory Open Access Journal |
| issn | 1475-2840 |
| language | English |
| last_indexed | 2024-04-12T15:03:10Z |
| publishDate | 2009-01-01 |
| publisher | BMC |
| record_format | Article |
| series | Cardiovascular Diabetology |
| spelling | doaj.art-49bc82389291461194d945532af0a5e82022-12-22T03:28:01ZengBMCCardiovascular Diabetology1475-28402009-01-0181410.1186/1475-2840-8-4Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteriesHowarth Frank CGurney Alison M<p>Abstract</p> <p>Background</p> <p>Poor control of blood glucose in diabetes is known to promote vascular dysfunction and hypertension. Diabetes was recently shown to be linked to an increased prevalence of pulmonary hypertension. The aim of this study was to determine how the pharmacological reactivity of intrapulmonary arteries is altered in a rat model of diabetes.</p> <p>Methods</p> <p>Diabetes was induced in rats by the β-cell toxin, streptozotocin (STZ, 60 mg/kg), and isolated conduit and resistance intrapulmonary arteries studied 3–4 months later. Isometric tension responses to the vasoconstrictors phenylephrine, serotonin and PGF<sub>2α</sub>, and the vasodilators carbachol and glyceryl trinitrate, were compared in STZ-treated rats and age-matched controls.</p> <p>Results</p> <p>STZ-induced diabetes significantly blunted the maximum response of conduit, but not resistance pulmonary arteries to phenylephrine and serotonin, without a change in pEC<sub>50</sub>. Agonist responses were differentially reduced, with serotonin (46% smaller) affected more than phenylephrine (32% smaller) and responses to PGF<sub>2α </sub>unaltered. Vasoconstriction caused by K<sup>+</sup>-induced depolarisation remained normal in diabetic rats. Endothelium-dependent dilation to carbachol and endothelium-independent dilation to glyceryl trinitrate were also unaffected.</p> <p>Conclusion</p> <p>The small resistance pulmonary arteries are relatively resistant to STZ-induced diabetes. The impaired constrictor responsiveness of conduit vessels was agonist dependent, suggesting possible loss of receptor expression or function. The observed effects cannot account for pulmonary hypertension in diabetes, rather the impaired reactivity to vasoconstrictors would counteract the development of pulmonary hypertensive disease.</p>http://www.cardiab.com/content/8/1/4 |
| spellingShingle | Howarth Frank C Gurney Alison M Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries Cardiovascular Diabetology |
| title | Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries |
| title_full | Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries |
| title_fullStr | Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries |
| title_full_unstemmed | Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries |
| title_short | Effects of streptozotocin-induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries |
| title_sort | effects of streptozotocin induced diabetes on the pharmacology of rat conduit and resistance intrapulmonary arteries |
| url | http://www.cardiab.com/content/8/1/4 |
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