نتایج جستجو برای: 4 hydroxy 2 nonenal

تعداد نتایج: 3126698  

Journal: :American journal of physiology. Lung cellular and molecular physiology 2006
Sabah N A Hussain Ghassan Matar Esther Barreiro Maria Florian Maziar Divangahi Theodoros Vassilakopoulos

Although 4-hydroxy-2-nonenal (HNE, a product of lipid peroxidation) is a major cause of oxidative damage inside skeletal muscles, the exact proteins modified by HNE are unknown. We used two-dimensional electrophoresis, immunoblotting, and mass spectrometry to identify selective proteins targeted by HNE inside the diaphragm of rats under two conditions: severe sepsis [induced by E. coli lipopoly...

Journal: :Free radical biology & medicine 2007
Takaaki Hayashi Naomi Shishido Kenji Nakayama Akihiko Nunomura Mark A Smith George Perry Masao Nakamura

The lipid peroxidation product 4-hydroxy-2-nonenal (HNE) is proposed to be a toxic factor in the pathogenesis of Alzheimer disease. The primary products of lipid peroxidation are phospholipid hydroperoxides, and degraded reactive aldehydes, such as HNE, are considered secondary peroxidation products. In this study, we investigated the role of amyloid-beta peptide (A beta) in the formation of ph...

2014
Taro Yamaguchi Reiko Nagashima Masanori Yoneyama Tatsuo Shiba Kiyokazu Ogita

Noise-induced hearing loss is at least in part due to disruption of endocochlear potential, which is maintained by various K(+) transport apparatuses including Na(+), K(+)-ATPase and gap junction-mediated intercellular communication in the lateral wall structures. In this study, we examined the changes in the ion-trafficking-related proteins in the spiral ligament fibrocytes (SLFs) following in...

Journal: :Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 2013

Journal: :Cancer research 1986
C K Winter H J Segall W F Haddon

trans-4-Hydroxy-2-hexenal (t-4HH), a reactive metabolite isolated from the pyrrolizidine alkaloid senecionine, and trans-4-hydroxy-2-nonenal (t-4HN), a product of lipid peroxidation, reacted nonenzymatically with deoxyguanosine at pH 7.4 at 37 degrees C in vitro with each compound yielding two pairs of diastereomeric adducts. Adducts were isolated using reverse phase high-performance liquid chr...

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