Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice
The objective of the present study was to assess the effects of the immunosuppressant rapamycin (Rapamune®, Sirolimus) on both resistance vessel responsiveness and atherosclerosis in apolipoprotein E-deficient 8-week-old male mice fed a normal rodent diet. Norepinephrine (NE)-induced vasoconstrictio...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Associação Brasileira de Divulgação Científica
2009-12-01
|
Series: | Brazilian Journal of Medical and Biological Research |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009001200012 |
id |
doaj-a5467e83f1324993afb783a3d3ccd16b |
---|---|
record_format |
Article |
spelling |
doaj-a5467e83f1324993afb783a3d3ccd16b2020-11-25T00:15:35ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2009-12-01421211911195Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient miceA.L.N. GadioliB.V. NogueiraR.M.P. ArrudaR.B. PereiraS.S. MeyrellesJ.A. ArrudaE.C. VasquezThe objective of the present study was to assess the effects of the immunosuppressant rapamycin (Rapamune®, Sirolimus) on both resistance vessel responsiveness and atherosclerosis in apolipoprotein E-deficient 8-week-old male mice fed a normal rodent diet. Norepinephrine (NE)-induced vasoconstriction, acetylcholine (ACh)- and sodium nitroprusside (SNP)-induced vasorelaxation of isolated mesenteric bed, and atherosclerotic lesions were evaluated. After 12 weeks of orally administered rapamycin (5 mg·kg-1·day-1, N = 9) and compared with untreated (control, N = 9) animals, rapamycin treatment did not modify either NE-induced vasoconstriction (maximal response: 114 ± 4 vs 124 ± 10 mmHg, respectively) or ACh- (maximal response: 51 ± 8 vs 53 ± 5%, respectively) and SNP-induced vasorelaxation (maximal response: 73 ± 6 vs 74 ± 6%, respectively) of the isolated vascular mesenteric bed. Despite increased total cholesterol in treated mice (982 ± 59 vs 722 ± 49 mg/dL, P < 0.01), lipid deposition on the aorta wall vessel was significantly less in rapamycin-treated animals (37 ± 12 vs 68 ± 8 µm² x 10³). These results indicate that orally administered rapamycin is effective in attenuating the progression of atherosclerotic plaque without affecting the responsiveness of resistance vessels, supporting the idea that this immunosuppressant agent might be of potential benefit against atherosclerosis in patients undergoing therapy.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009001200012RapamycinSirolimusAtherosclerosisVascular responsivenessApolipoprotein EMice |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
A.L.N. Gadioli B.V. Nogueira R.M.P. Arruda R.B. Pereira S.S. Meyrelles J.A. Arruda E.C. Vasquez |
spellingShingle |
A.L.N. Gadioli B.V. Nogueira R.M.P. Arruda R.B. Pereira S.S. Meyrelles J.A. Arruda E.C. Vasquez Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice Brazilian Journal of Medical and Biological Research Rapamycin Sirolimus Atherosclerosis Vascular responsiveness Apolipoprotein E Mice |
author_facet |
A.L.N. Gadioli B.V. Nogueira R.M.P. Arruda R.B. Pereira S.S. Meyrelles J.A. Arruda E.C. Vasquez |
author_sort |
A.L.N. Gadioli |
title |
Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice |
title_short |
Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice |
title_full |
Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice |
title_fullStr |
Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice |
title_full_unstemmed |
Oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein E-deficient mice |
title_sort |
oral rapamycin attenuates atherosclerosis without affecting the arterial responsiveness of resistance vessels in apolipoprotein e-deficient mice |
publisher |
Associação Brasileira de Divulgação Científica |
series |
Brazilian Journal of Medical and Biological Research |
issn |
0100-879X 1414-431X |
publishDate |
2009-12-01 |
description |
The objective of the present study was to assess the effects of the immunosuppressant rapamycin (Rapamune®, Sirolimus) on both resistance vessel responsiveness and atherosclerosis in apolipoprotein E-deficient 8-week-old male mice fed a normal rodent diet. Norepinephrine (NE)-induced vasoconstriction, acetylcholine (ACh)- and sodium nitroprusside (SNP)-induced vasorelaxation of isolated mesenteric bed, and atherosclerotic lesions were evaluated. After 12 weeks of orally administered rapamycin (5 mg·kg-1·day-1, N = 9) and compared with untreated (control, N = 9) animals, rapamycin treatment did not modify either NE-induced vasoconstriction (maximal response: 114 ± 4 vs 124 ± 10 mmHg, respectively) or ACh- (maximal response: 51 ± 8 vs 53 ± 5%, respectively) and SNP-induced vasorelaxation (maximal response: 73 ± 6 vs 74 ± 6%, respectively) of the isolated vascular mesenteric bed. Despite increased total cholesterol in treated mice (982 ± 59 vs 722 ± 49 mg/dL, P < 0.01), lipid deposition on the aorta wall vessel was significantly less in rapamycin-treated animals (37 ± 12 vs 68 ± 8 µm² x 10³). These results indicate that orally administered rapamycin is effective in attenuating the progression of atherosclerotic plaque without affecting the responsiveness of resistance vessels, supporting the idea that this immunosuppressant agent might be of potential benefit against atherosclerosis in patients undergoing therapy. |
topic |
Rapamycin Sirolimus Atherosclerosis Vascular responsiveness Apolipoprotein E Mice |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009001200012 |
work_keys_str_mv |
AT alngadioli oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice AT bvnogueira oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice AT rmparruda oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice AT rbpereira oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice AT ssmeyrelles oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice AT jaarruda oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice AT ecvasquez oralrapamycinattenuatesatherosclerosiswithoutaffectingthearterialresponsivenessofresistancevesselsinapolipoproteinedeficientmice |
_version_ |
1725386060883558400 |