نتایج جستجو برای: SCO2

تعداد نتایج: 217  

2015
Cheng Ni Ting Xu Nan Li Yang Tian Yongzheng Han Qingsheng Xue Min Li Xiangyang Guo

BACKGROUND Postoperative cognitive dysfunction (POCD) is a frequent complication in elderly patients undergoing major non-cardiac surgery, but its etiology is still unclear. Cerebral oxygen saturation (ScO2) represents the balance of cerebral oxygen supply and demand. The aim of present study was to evaluate the relationship between perioperative ScO2 and POCD, and to verify the hypothesis that...

2017
Hiroshi Mukaida Masakazu Hayashida Satoshi Matsushita Makiko Yamamoto Atsushi Nakamura Atsushi Amano

PURPOSE A previous study reported that low baseline cerebral oxygen saturation (ScO2) (≤50%) measured with near-infrared spectroscopy was predictive of poor clinical outcomes after cardiac surgery. However, such findings have not been reconfirmed by others. We conducted the current study to evaluate whether the previous findings would be reproducible, and to explore mechanisms underlying the Sc...

Journal: :Anesthesiology 2012
Henrik Sørensen Niels H Secher Christoph Siebenmann Henning B Nielsen Matthias Kohl-Bareis Carsten Lundby Peter Rasmussen

BACKGROUND Perioperative optimization of spatially resolved near-infrared spectroscopy determined cerebral frontal lobe oxygenation (scO2) may reduce postoperative morbidity. Norepinephrine is routinely administered to maintain cerebral perfusion pressure and, thereby, cerebral blood flow, but norepinephrine reduces the scO2. We hypothesized that norepinephrine-induced reduction in scO2 is infl...

Journal: :Archives of neurology 2004
Stacey K H Tay Sara Shanske Paige Kaplan Salvatore DiMauro

BACKGROUND SCO2 is a cytochrome c oxidase (COX) assembly gene that encodes a mitochondrial inner membrane protein that probably functions as a copper transporter. Mutations in SCO2 have been associated with severe COX deficiency and early-onset fatal infantile hypertrophic cardiomyopathy, encephalopathy, and neurogenic muscle atrophy. Fetal wastage has not been described in association with mut...

Journal: :Circulation. Heart failure 2012
Hideo Nakamura Satoaki Matoba Eri Iwai-Kanai Masaki Kimata Atsushi Hoshino Mikihiko Nakaoka Maki Katamura Yoshifumi Okawa Makoto Ariyoshi Yuichiro Mita Koji Ikeda Mitsuhiko Okigaki Souichi Adachi Hideo Tanaka Tetsuro Takamatsu Hiroaki Matsubara

BACKGROUND Diabetic cardiomyopathy is characterized by energetic dysregulation caused by glucotoxicity, lipotoxicity, and mitochondrial alterations. p53 and its downstream mitochondrial assembly protein, synthesis of cytochrome c oxidase 2 (SCO2), are important regulators of mitochondrial respiration, whereas the involvement in diabetic cardiomyopathy remains to be determined. METHODS AND RES...

Journal: :The Biochemical journal 2005
Lukas Stiburek Katerina Vesela Hana Hansikova Petr Pecina Marketa Tesarova Leona Cerna Josef Houstek Jiri Zeman

The biogenesis of eukaryotic COX (cytochrome c oxidase) requires several accessory proteins in addition to structural subunits and prosthetic groups. We have analysed the assembly state of COX and SCO2 protein levels in various tissues of six patients with mutations in SCO2 and SURF1. SCO2 is a copper-binding protein presumably involved in formation of the Cu(A) centre of the COX2 subunit. The ...

2014
Henrik Sørensen Hilary P. Grocott Mads Niemann Allan Rasmussen Jens G. Hillingsø Hans J. Frederiksen Niels H. Secher

BACKGROUND As measured by near infrared spectroscopy (NIRS), cerebral oxygenation (ScO2) may be reduced by hyperventilation in the anhepatic phase of liver transplantation surgery (LTx). Conversely, the brain may be subjected to hyperperfusion during reperfusion of the grafted liver. We investigated the relationship between ScO2 and end-tidal CO2 tension (EtCO2) during the various phases of LTx...

Journal: :Human molecular genetics 2009
Scot C Leary Florin Sasarman Tamiko Nishimura Eric A Shoubridge

Human SCO1 and SCO2 code for essential metallochaperones with ill-defined functions in the biogenesis of the CuA site of cytochrome c oxidase subunit II (CO II). Here, we have used patient cell lines to investigate the specific roles of each SCO protein in this pathway. By pulse-labeling mitochondrial translation products, we demonstrate that the synthesis of CO II is reduced in SCO2, but not i...

Journal: :Human molecular genetics 2001
M Jaksch C Paret R Stucka N Horn J Müller-Höcker R Horvath N Trepesch G Stecker P Freisinger C Thirion J Müller R Lunkwitz G Rödel E A Shoubridge H Lochmüller

Mutations in SCO2, a cytochrome c oxidase (COX) assembly gene, have been reported in nine infants with early onset fatal cardioencephalomyopathy and a severe COX deficiency in striated muscle. Studies on a yeast homolog have suggested that human Sco2 acts as a copper chaperone, transporting copper to the Cu(A) site on the Cox II subunit, but the mechanism of action remains unclear. To investiga...

2018
Tova Hallas Binyamin Eisen Yuval Shemer Ronen Ben Jehuda Lucy N Mekies Shulamit Naor Revital Schick Sivan Eliyahu Irina Reiter Eugene Vlodavsky Yeshayahu Shai Katz Katrin Õunap Avraham Lorber Richard Rodenburg Hanna Mandel Mihaela Gherghiceanu Ofer Binah

Mutations in SCO2 are among the most common causes of COX deficiency, resulting in reduced mitochondrial oxidative ATP production capacity, often leading to hypertrophic cardiomyopathy (HCM). To date, none of the recent pertaining reports provide deep understanding of the SCO2 disease pathophysiology. To investigate the cardiac pathology of the disease, we were the first to generate induced plu...

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