Matches in SemOpenAlex for { <https://semopenalex.org/work/W1987017017> ?p ?o ?g. }
- W1987017017 endingPage "616" @default.
- W1987017017 startingPage "607" @default.
- W1987017017 abstract "Low protein diet mediated renoprotection in remnant kidneys: Renal autoregulatory versus hypertrophic mechanisms.BackgroundThe mechanism of low protein diet conferred renoprotection in the ablation model remains controversial. Blockade of glomerular hypertrophy, reduced preglomerular vasodilation, and preserved autoregulation have all been postulated. The potential differential impact of calcium channel blockers on these mechanisms and glomerulosclerosis was examined.MethodsRats with 5/6 renal ablation received either a 25% standard protein diet, an 8% low protein diet and a low protein diet with either verapamil or amlodipine. Renal autoregulatory and morphometric studies were performed at 3 weeks before the development of significant injury, and the assessment of glomerulosclerosis after 7 weeks of continuous blood pressure radiotelemetry in additional rats.ResultsThe preserved renal autoregulation in low protein rats was abolished by both calcium channel blockers, with the impairment being either comparable to (low protein + verapamil) or greater than the standard protein rats (low protein + amlodipine). Neither calcium channel blocker blocked the inhibitory effects of low protein diet on renal blood flow, kidney weight, and glomerular volume. Results (mean ± SE) for glomerular volume (μm-3× 10-6): low protein (N = 11), 1.6 ± 0.1; low protein + verapamil (N = 10), 1.7 ± 0.1; low protein + amlodipine (N = 12), 1.7 ± 0.2; versus standard protein (N = 10), 2.2 ± 0.1; P < 0.05. Only amlodipine, but not verapamil, reduced average systolic blood pressure (143 ± 2 mm Hg versus low protein rats, 168 ± 5 mm Hg, and standard rats, 170 ± 6 mm Hg; P < 0.01). Nevertheless, the glomeruloprotection seen in low protein (N = 15) as compared to standard protein (N = 14) rats (9%± 3% versus 28%± 6% glomerulosclerosis; P < 0.01) was abolished in both low protein + verapamil (N = 14, 32%± 7%) and low protein + amlodipine rats (N = 16, 27%± 7%).ConclusionsPreservation of renal autoregulation and not inhibition of hypertrophy is the critical component in low protein diet-conferred glomeruloprotection. Low protein diet mediated renoprotection in remnant kidneys: Renal autoregulatory versus hypertrophic mechanisms. The mechanism of low protein diet conferred renoprotection in the ablation model remains controversial. Blockade of glomerular hypertrophy, reduced preglomerular vasodilation, and preserved autoregulation have all been postulated. The potential differential impact of calcium channel blockers on these mechanisms and glomerulosclerosis was examined. Rats with 5/6 renal ablation received either a 25% standard protein diet, an 8% low protein diet and a low protein diet with either verapamil or amlodipine. Renal autoregulatory and morphometric studies were performed at 3 weeks before the development of significant injury, and the assessment of glomerulosclerosis after 7 weeks of continuous blood pressure radiotelemetry in additional rats. The preserved renal autoregulation in low protein rats was abolished by both calcium channel blockers, with the impairment being either comparable to (low protein + verapamil) or greater than the standard protein rats (low protein + amlodipine). Neither calcium channel blocker blocked the inhibitory effects of low protein diet on renal blood flow, kidney weight, and glomerular volume. Results (mean ± SE) for glomerular volume (μm-3× 10-6): low protein (N = 11), 1.6 ± 0.1; low protein + verapamil (N = 10), 1.7 ± 0.1; low protein + amlodipine (N = 12), 1.7 ± 0.2; versus standard protein (N = 10), 2.2 ± 0.1; P < 0.05. Only amlodipine, but not verapamil, reduced average systolic blood pressure (143 ± 2 mm Hg versus low protein rats, 168 ± 5 mm Hg, and standard rats, 170 ± 6 mm Hg; P < 0.01). Nevertheless, the glomeruloprotection seen in low protein (N = 15) as compared to standard protein (N = 14) rats (9%± 3% versus 28%± 6% glomerulosclerosis; P < 0.01) was abolished in both low protein + verapamil (N = 14, 32%± 7%) and low protein + amlodipine rats (N = 16, 27%± 7%). Preservation of renal autoregulation and not inhibition of hypertrophy is the critical component in low protein diet-conferred glomeruloprotection." @default.
- W1987017017 created "2016-06-24" @default.
- W1987017017 creator A5009121656 @default.
- W1987017017 creator A5015269108 @default.
- W1987017017 creator A5071788399 @default.
- W1987017017 creator A5090125195 @default.
- W1987017017 date "2003-02-01" @default.
- W1987017017 modified "2023-09-23" @default.
- W1987017017 title "Low protein diet mediated renoprotection in remnant kidneys: Renal autoregulatory versus hypertrophic mechanisms" @default.
- W1987017017 cites W1964830572 @default.
- W1987017017 cites W1975755598 @default.
- W1987017017 cites W1985133368 @default.
- W1987017017 cites W1989996614 @default.
- W1987017017 cites W1995286167 @default.
- W1987017017 cites W1998509977 @default.
- W1987017017 cites W2006900591 @default.
- W1987017017 cites W2011497717 @default.
- W1987017017 cites W2015725644 @default.
- W1987017017 cites W2016400390 @default.
- W1987017017 cites W2025763306 @default.
- W1987017017 cites W2027785852 @default.
- W1987017017 cites W2036393060 @default.
- W1987017017 cites W2051195819 @default.
- W1987017017 cites W2055296168 @default.
- W1987017017 cites W2057353595 @default.
- W1987017017 cites W2084473470 @default.
- W1987017017 cites W2090276658 @default.
- W1987017017 cites W2094052501 @default.
- W1987017017 cites W2094698265 @default.
- W1987017017 cites W2096816041 @default.
- W1987017017 cites W2107442450 @default.
- W1987017017 cites W2116012941 @default.
- W1987017017 cites W2129823783 @default.
- W1987017017 cites W2138443098 @default.
- W1987017017 cites W2144403565 @default.
- W1987017017 cites W2147350752 @default.
- W1987017017 cites W2147804563 @default.
- W1987017017 cites W2168234252 @default.
- W1987017017 cites W2173448119 @default.
- W1987017017 cites W2231812784 @default.
- W1987017017 cites W2243393341 @default.
- W1987017017 cites W3023346164 @default.
- W1987017017 cites W3030237074 @default.
- W1987017017 doi "https://doi.org/10.1046/j.1523-1755.2003.00759.x" @default.
- W1987017017 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12631125" @default.
- W1987017017 hasPublicationYear "2003" @default.
- W1987017017 type Work @default.
- W1987017017 sameAs 1987017017 @default.
- W1987017017 citedByCount "20" @default.
- W1987017017 countsByYear W19870170172015 @default.
- W1987017017 countsByYear W19870170172016 @default.
- W1987017017 countsByYear W19870170172017 @default.
- W1987017017 countsByYear W19870170172018 @default.
- W1987017017 countsByYear W19870170172022 @default.
- W1987017017 crossrefType "journal-article" @default.
- W1987017017 hasAuthorship W1987017017A5009121656 @default.
- W1987017017 hasAuthorship W1987017017A5015269108 @default.
- W1987017017 hasAuthorship W1987017017A5071788399 @default.
- W1987017017 hasAuthorship W1987017017A5090125195 @default.
- W1987017017 hasBestOaLocation W19870170171 @default.
- W1987017017 hasConcept C126322002 @default.
- W1987017017 hasConcept C134018914 @default.
- W1987017017 hasConcept C142225936 @default.
- W1987017017 hasConcept C2777022698 @default.
- W1987017017 hasConcept C2777661713 @default.
- W1987017017 hasConcept C2779646130 @default.
- W1987017017 hasConcept C2780091579 @default.
- W1987017017 hasConcept C2780356492 @default.
- W1987017017 hasConcept C519063684 @default.
- W1987017017 hasConcept C71924100 @default.
- W1987017017 hasConcept C84393581 @default.
- W1987017017 hasConceptScore W1987017017C126322002 @default.
- W1987017017 hasConceptScore W1987017017C134018914 @default.
- W1987017017 hasConceptScore W1987017017C142225936 @default.
- W1987017017 hasConceptScore W1987017017C2777022698 @default.
- W1987017017 hasConceptScore W1987017017C2777661713 @default.
- W1987017017 hasConceptScore W1987017017C2779646130 @default.
- W1987017017 hasConceptScore W1987017017C2780091579 @default.
- W1987017017 hasConceptScore W1987017017C2780356492 @default.
- W1987017017 hasConceptScore W1987017017C519063684 @default.
- W1987017017 hasConceptScore W1987017017C71924100 @default.
- W1987017017 hasConceptScore W1987017017C84393581 @default.
- W1987017017 hasIssue "2" @default.
- W1987017017 hasLocation W19870170171 @default.
- W1987017017 hasLocation W19870170172 @default.
- W1987017017 hasOpenAccess W1987017017 @default.
- W1987017017 hasPrimaryLocation W19870170171 @default.
- W1987017017 hasRelatedWork W1978618357 @default.
- W1987017017 hasRelatedWork W2021486511 @default.
- W1987017017 hasRelatedWork W2037982983 @default.
- W1987017017 hasRelatedWork W2039411940 @default.
- W1987017017 hasRelatedWork W2042033030 @default.
- W1987017017 hasRelatedWork W2052759325 @default.
- W1987017017 hasRelatedWork W2076192765 @default.
- W1987017017 hasRelatedWork W2127085070 @default.
- W1987017017 hasRelatedWork W2400445066 @default.
- W1987017017 hasRelatedWork W4244936725 @default.
- W1987017017 hasVolume "63" @default.