Document Information


PMID 9675268  (  )
Title Effects of mitochondrial respiratory stimulation on membrane lipids and proteins: an electron paramagnetic resonance investigation.
Abstract Previous studies have implicated mitochondria-derived reactive oxygen species (ROS) in both the aging process and age-related diseases such as Alzheimer's disease, amyotrophic lateral sclerosis, Parkinson's disease etc. The current study, utilizing electron paramagnetic resonance (EPR) spectrometry, was designed to determine if mitochondrial respiratory stimulation, under state 4 conditions, caused extensive oxidative modifications to membrane cytoskeletal proteins and lipids in the brain. A mixed population of cortical synaptosomes and mitochondria, prepared by centrifugation techniques using rat brain cortex from adult (4-6 months) female Brown Norway rat brains, were labeled with the lipid-specific spin probe, 5-nitroxyl stearate (5-NS). Stimulation of the mitochondrial electron transport chain was accomplished using 20 mM succinate at 25 degrees C for 3 h. Mitochondrially derived free radicals, when reacted with the paramagnetic center of the spin probe, result in a loss of paramagnetism resulting in loss of intensity. A significant lowering (23%, P<0.0001) in the signal amplitude (B0) of 5-NS, indicative of generation of oxyradicals, was found. The order parameter, an inverse EPR-measure of membrane fluidity of the 5-NS spin labeled mitochondrial and synaptosomal membranes, also decreased following mitochondrial respiratory stimulation (P<0.005). Changes in the physical state of cytoskeletal and transmembrane proteins due to succinate oxidation were measured using MAL-6 (2,2,6, 6,-tetramethyl-4 maleimidopiperdin-1-oxyl), a thiol-specific nitroxide spin label. The ratio of the amplitudes of the weakly to strongly immobilized spin label reaction sites (W/S ratio) in the low-field region of the spectrum was used to determine any alteration in protein conformation. Previous studies in our laboratory have established that increased protein oxidation is associated with a decreased W/S ratio. In the current study, our results indicated significant lowering of the W/S ratio in cortex (30%, P<0.0001) upon stimulation of the mitochondria with 20 mM succinate. Thus, we conclude that respiratory stimulation of mitochondria, due to a hypermetabolic stress with succinate, caused significant oxidative modifications of cortical membrane lipids and proteins. USA.

NOTE: Color highlight is limited to the abstract and SciMiner text-mining mode. If you see much more identified targets below from "Targets by SciMiner Summary" and "Targets by SciMiner Full list", they may have been identified from the full text.



Targets by SciMiner Summary

HUGO ID Symbol Target Name #Occur ActualStr
6817MALmal, T-cell differentiation protein3MAL-6-labeled | MAL-6-linked | MAL-6-spin |
620APPamyloid beta (A4) precursor protein (peptidase nexin-II, Alzheimer disease)1amyloid |
7873NOS2Anitric oxide synthase 2A (inducible, hepatocytes)1nitric oxide synthase |
12805XDHxanthine dehydrogenase1xanthine oxidase |

 


Targets by SciMiner Full list

HUGO ID Symbol Name ActualStr Score FlankingText
6817MALmal, T-cell differentiation proteinMAL-6-linked0.6in our laboratory of the W / S ratio of MAL-6-linked synaptosomal membrane following 4-HNE treatment have shown that this toxic
6817MALmal, T-cell differentiation proteinMAL-6-spin0.6as monitored by a reduced W / S ratio of MAL-6-spin labeled synaptosomal membranes 36
6817MALmal, T-cell differentiation proteinMAL-6-labeled0.6generation 21 in which the W / S ratio of MAL-6-labeled neocortical or erythrocyte membranes was reduced 21 30 31 32
620APPamyloid beta (A4) precursor protein (peptidase nexin-II, Alzheimer disease)amyloid1.0and peptides (e.g e.g nitric oxide synthase xanthine oxidase _amp_#x3b2 -amyloid etc. present in the brain
7873NOS2Anitric oxide synthase 2A (inducible, hepatocytes)nitric oxide synthase1.0oxidative insult to normal neurons also results from catalytically active redox metal ions i.e iron and copper and particular ros generating enzymes and peptides e.g nitric oxide synthase xanthine oxidase _amp_#x3b2; amyloid etc. present in the brain.
12805XDHxanthine dehydrogenasexanthine oxidase1.0oxidative insult to normal neurons also results from catalytically active redox metal ions i.e iron and copper and particular ros generating enzymes and peptides e.g nitric oxide synthase xanthine oxidase _amp_#x3b2; amyloid etc. present in the brain.