-
Something wrong with this record ?
RhoA distribution in renal caveolar fractions in experimental type 1 diabetes
Demová H, Černá M.
Language English Country Czech Republic
Document type Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
ProQuest Central
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
- MeSH
- Angiotensin Receptor Antagonists therapeutic use MeSH
- Diabetes Mellitus, Type 1 drug therapy metabolism MeSH
- Diabetes Mellitus, Experimental drug therapy metabolism MeSH
- Immunoprecipitation MeSH
- Caveolin 1 metabolism MeSH
- Caveolae metabolism MeSH
- Rats MeSH
- Losartan therapeutic use MeSH
- Random Allocation MeSH
- Rats, Wistar MeSH
- rhoA GTP-Binding Protein metabolism MeSH
- Blotting, Western MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
Caveolae act as signalling platforms serving as concentrating points for numerous signalling molecules, as well as regulating flux through many distinct signalling cascades. RhoA proteins have been identified as potential actors in the pathophysiology of the cardiovascular system. We used sucrose gradient fractionation and immunoblotting to determine caveolin-1 and RhoA presence in the kidney cortex of streptozotocin-induced T1 diabetes rats (4-week duration), and of diabetic rats treated with angiotensin receptor blocker losartan (4 weeks, 20 mg/kg/day) to retard renal hypertension. Positive RhoA/caveolin-1 co-immunoprecipitation result was detected in the caveolar fraction that corresponded to the light-scattering band obtained from diabetic rats, compared to negative co-immunoprecipitation result in the caveolar fraction obtained from control rats. The detection of RhoA protein in the caveolar fractions and the prospective RhoA/caveolin-1 association can be used to examine the role of these signalling reactions in the pathophysiology of microvascular complications in type 1 diabetes
Literatura
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12000298
- 003
- CZ-PrNML
- 005
- 20120619145413.0
- 007
- ta
- 008
- 120112s2011 xr d f 000 0eng||
- 009
- AR
- 035 __
- $a (PubMed)21978755
- 040 __
- $a ABA008 $d ABA008 $e AACR2 $b cze
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Demová, Hana $7 xx0115679 $u Diabetes Center, Institute for Clinical and Experimental Medicine, Prague
- 245 10
- $a RhoA distribution in renal caveolar fractions in experimental type 1 diabetes / $c Demová H, Černá M.
- 504 __
- $a Literatura $b 33
- 520 9_
- $a Caveolae act as signalling platforms serving as concentrating points for numerous signalling molecules, as well as regulating flux through many distinct signalling cascades. RhoA proteins have been identified as potential actors in the pathophysiology of the cardiovascular system. We used sucrose gradient fractionation and immunoblotting to determine caveolin-1 and RhoA presence in the kidney cortex of streptozotocin-induced T1 diabetes rats (4-week duration), and of diabetic rats treated with angiotensin receptor blocker losartan (4 weeks, 20 mg/kg/day) to retard renal hypertension. Positive RhoA/caveolin-1 co-immunoprecipitation result was detected in the caveolar fraction that corresponded to the light-scattering band obtained from diabetic rats, compared to negative co-immunoprecipitation result in the caveolar fraction obtained from control rats. The detection of RhoA protein in the caveolar fractions and the prospective RhoA/caveolin-1 association can be used to examine the role of these signalling reactions in the pathophysiology of microvascular complications in type 1 diabetes
- 650 _2
- $a antagonisté receptorů pro angiotenzin $x terapeutické užití $7 D057911
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a western blotting $7 D015153
- 650 _2
- $a kaveoly $x metabolismus $7 D021941
- 650 _2
- $a kaveolin 1 $x metabolismus $7 D051242
- 650 _2
- $a experimentální diabetes mellitus $x farmakoterapie $x metabolismus $7 D003921
- 650 _2
- $a diabetes mellitus 1. typu $x farmakoterapie $x metabolismus $7 D003922
- 650 _2
- $a imunoprecipitace $7 D047468
- 650 _2
- $a losartan $x terapeutické užití $7 D019808
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a náhodné rozdělení $7 D011897
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a rhoA protein vázající GTP $x metabolismus $7 D020742
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Černá, Marie, $d 1964- $7 mzk2004258459 $u Institute of General Biology and Genetics, Third Faculty of Medicine, Charles University in Prague, Prague, Czech Republic
- 773 0_
- $t Folia biologica $x 0015-5500 $g Roč. 57, č. 4 (2011), s. 139-144 $w MED00011004
- 856 41
- $u https://fb.cuni.cz/file/5592/FB2011A0021.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 970 $c 89 $y 2
- 990 __
- $a 20120112101500 $b ABA008
- 991 __
- $a 20120619145336 $b ABA008
- 999 __
- $a ok $b bmc $g 892979 $s 756973
- BAS __
- $a 3
- BMC __
- $a 2011 $b 57 $c 4 $d 139-144 $i 0015-5500 $m Folia biologica (Praha) $n Folia biol. (Praha) $x MED00011004
- LZP __
- $a 2012-01/mkme