Effects of Hyperoxia on Mitochondrial Multienzyme Complex Ⅲ and Ⅴ in Premature Newborn Rat Lung
To investigate the effects of hyperoxia on mitochondrial multienzyme complex Ⅲ (cytochrome, Cytb) and Ⅴ (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group, The rats in hyperoxia group were continuously exposed to 85% oxyg...
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Published in | Journal of Huazhong University of Science and Technology. Medical sciences Vol. 28; no. 2; pp. 207 - 210 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Huazhong University of Science and Technology
01.04.2008
Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China |
Subjects | |
Online Access | Get full text |
ISSN | 1672-0733 1993-1352 |
DOI | 10.1007/s11596-008-0224-4 |
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Abstract | To investigate the effects of hyperoxia on mitochondrial multienzyme complex Ⅲ (cytochrome, Cytb) and Ⅴ (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group, The rats in hyperoxia group were continuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased (P〉0,05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant (P〉0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure (P〈0.05) and did not show any significant change 4, 7, 10 days after the exposure (P〉0.05). At the 14th day, ATPase6 mRNA expression was significantly increased (P〈0.05), ATPase8 mRNA expression did not show any significant change 1, 4, 10 day(s) after the exposure (P〉0.05), At the 7th and 14th day, ATPase8 mRNA expression was significantly increased (P〈0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant (P〉0.05). The general tendency was decreased after 7 days, and its expression became weak but difference was not significant 7, 10 days after the exposure (P〉0.05). At day 14 its expression became significantly weak (P〈0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury. |
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AbstractList | To investigate the effects of hyperoxia on mitochondrial multienzyme complex III (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group. The rats in hyperoxia group were continuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased (P>0.05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant (P>0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure (P<0.05) and did not show any significant change 4, 7, 10 days after the exposure (P>0.05). At the 14th day, ATPase6 mRNA expression was significantly increased (P<0.05). ATPase8 mRNA expression did not show any significant change 1, 4, 10 day(s) after the exposure (P>0.05). At the 7th and 14th day, ATPase8 mRNA expression was significantly increased (P<0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant (P>0.05). The general tendency was decreased after 7 days, and its expression became weak but difference was not significant 7, 10 days after the exposure (P>0.05). At day 14 its expression became significantly weak (P<0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury.To investigate the effects of hyperoxia on mitochondrial multienzyme complex III (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group. The rats in hyperoxia group were continuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased (P>0.05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant (P>0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure (P<0.05) and did not show any significant change 4, 7, 10 days after the exposure (P>0.05). At the 14th day, ATPase6 mRNA expression was significantly increased (P<0.05). ATPase8 mRNA expression did not show any significant change 1, 4, 10 day(s) after the exposure (P>0.05). At the 7th and 14th day, ATPase8 mRNA expression was significantly increased (P<0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant (P>0.05). The general tendency was decreased after 7 days, and its expression became weak but difference was not significant 7, 10 days after the exposure (P>0.05). At day 14 its expression became significantly weak (P<0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury. Summary To investigate the effects of hyperoxia on mitochondrial multienzyme complex III (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group. The rats in hyperoxia group were continuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased ( P >0.05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant ( P >0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure ( P <0.05) and did not show any significant change 4, 7, 10 days after the exposure ( P >0.05). At the 14th day, ATPase6 mRNA expression was significantly increased ( P <0.05). ATPase8 mRNA expression did not show any significant change 1, 4, 10 day(s) after the exposure ( P >0.05). At the 7th and 14th day, ATPase8 mRNA expression was significantly increased ( P <0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant ( P >0.05). The general tendency was decreased after 7 days, and its expression became weak but difference was not significant 7, 10 days after the exposure ( P >0.05). At day 14 its expression became significantly weak ( P <0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury. R3; To investigate the effects of hyperoxia on mitochondrial multienzyme complex Ⅲ (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the l-day-old preterrn SD rats were randomly assigned to hyperoxia group and air group. The rats in hyperoxia group were con- tinuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased (P>0.05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant (P>0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure (P<0.05) and did not show any significant change 4, 7, 10 days after the exposure (P>0.05). At the 14th day, ATPase6 mRNA expression was significantly increased (P<0.05). ATPase8 mRNA expression did not show any significant change 1, 4, l0 day(s) after the exposure (P>0.05). At the 7th and 14th day, ATPase8 mRNA expression was significantly increased (P<0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant (P>0.05). The gen- eral tendency was decreased after 7 days, and its expression became weak but difference was not sig- nificant 7, 10 days after the exposure (P>0.05). At day 14 its expression became significantly weak (P<0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury. To investigate the effects of hyperoxia on mitochondrial multienzyme complex Ⅲ (cytochrome, Cytb) and Ⅴ (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group, The rats in hyperoxia group were continuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased (P〉0,05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant (P〉0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure (P〈0.05) and did not show any significant change 4, 7, 10 days after the exposure (P〉0.05). At the 14th day, ATPase6 mRNA expression was significantly increased (P〈0.05), ATPase8 mRNA expression did not show any significant change 1, 4, 10 day(s) after the exposure (P〉0.05), At the 7th and 14th day, ATPase8 mRNA expression was significantly increased (P〈0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant (P〉0.05). The general tendency was decreased after 7 days, and its expression became weak but difference was not significant 7, 10 days after the exposure (P〉0.05). At day 14 its expression became significantly weak (P〈0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury. To investigate the effects of hyperoxia on mitochondrial multienzyme complex III (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the 1-day-old preterm SD rats were randomly assigned to hyperoxia group and air group. The rats in hyperoxia group were continuously exposed to 85% oxygen and those in air group to room air. After 1, 4, 7, 10, 14 day(s) of exposure, these rats were killed, total lung RNA was extracted and Cytb, ATPase6, 8 mRNA were detected by reverse transcription polymerase chain reaction (RT-PCR). Western blotting was used to detect the expression of Cytb protein in lung tissue. The results showed that compared with air group, Cytb mRNA expression was significantly increased (P>0.05) after 1, 4 day(s) of exposure. The general tendency decreased after 7 days, and its expression became weak but difference in mRNA expression between the two groups was not significant (P>0.05). ATPase6 mRNA expression was significantly increased 1 day after the exposure (P<0.05) and did not show any significant change 4, 7, 10 days after the exposure (P>0.05). At the 14th day, ATPase6 mRNA expression was significantly increased (P<0.05). ATPase8 mRNA expression did not show any significant change 1, 4, 10 day(s) after the exposure (P>0.05). At the 7th and 14th day, ATPase8 mRNA expression was significantly increased (P<0.05). Western blotting showed that Cytb protein expression was increased 1,4 day(s) after the exposure, but the difference between the two groups was not significant (P>0.05). The general tendency was decreased after 7 days, and its expression became weak but difference was not significant 7, 10 days after the exposure (P>0.05). At day 14 its expression became significantly weak (P<0.05). We are led to conclude that exposure to high concentrations of oxygen can significantly change the expression of Cytb and ATPase6, 8, which results in uncoupling of oxidative phosphorylation in mitochondrial respiration chain, and plays an important role in the mechanism of hyperoxia-induced lung injury. |
Author | 蔡成 常立文 李文斌 刘伟 |
AuthorAffiliation | Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology; Wuhan 430030, China |
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Cites_doi | 10.1007/s10541-005-0106-3 10.1074/jbc.M404993200 10.1371/journal.pcbi.0010036 10.1371/journal.pbio.0050259 10.1073/pnas.0601149103 10.1128/EC.4.2.346-355.2005 10.1016/j.neuint.2007.02.003 10.1016/S0006-3495(04)74205-8 10.1186/1465-9921-8-41 10.1186/1471-2466-6-8 10.1165/ajrcmb.25.2.4362 10.1007/BF02873565 |
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References | Esser, Gong, Yang (CR10) 2006; 103 Rea, Ventura, Johnson (CR6) 2007; 5 Beard (CR11) 2005; 1 Chang (CR4) 2007; 22 Valerie, Cory, Brigid (CR7) 2005; 4 Anantharam, Lehrmann, Kanthasamy (CR14) 2007; 50 Ballard, Anstead, Shook (CR13) 2007; 8 Li, Lu, Liu (CR9) 2004; 14 Aksimentiev, Balabin, Fillingame (CR8) 2004; 86 Ono, Sone, Yoshida (CR12) 2004; 279 Ter Horst, Fijlstra, Sengupta (CR2) 2006; 6 Chernyak, Pletjushkina, Izyumov (CR5) 2005; 70 Wang, Chang, Li (CR3) 2005; 25 McGratn-Morrow, Stah (CR1) 2001; 25 B. V. Chernyak (224_CR5) 2005; 70 S. Ono (224_CR12) 2004; 279 V. Anantharam (224_CR14) 2007; 50 D.A. Beard (224_CR11) 2005; 1 S. A. McGratn-Morrow (224_CR1) 2001; 25 A. Aksimentiev (224_CR8) 2004; 86 E. G. Valerie (224_CR7) 2005; 4 L. Esser (224_CR10) 2006; 103 H. Wang (224_CR3) 2005; 25 L. W. Chang (224_CR4) 2007; 22 S. L. Rea (224_CR6) 2007; 5 H. O. Ballard (224_CR13) 2007; 8 W. W. Li (224_CR9) 2004; 14 S. A. Horst Ter (224_CR2) 2006; 6 16116961 - J Huazhong Univ Sci Technolog Med Sci. 2005;25(2):159-61, 165 16163394 - PLoS Comput Biol. 2005 Sep;1(4):e36 14990464 - Biophys J. 2004 Mar;86(3):1332-44 17914900 - PLoS Biol. 2007 Oct 2;5(10):e259 17397968 - Neurochem Int. 2007 May;50(6):834-47 15807664 - Biochemistry (Mosc). 2005 Feb;70(2):240-5 16924113 - Proc Natl Acad Sci U S A. 2006 Aug 29;103(35):13045-50 17550598 - Respir Res. 2007 Jun 05;8:41 16620381 - BMC Pulm Med. 2006 Apr 18;6:8 15701797 - Eukaryot Cell. 2005 Feb;4(2):346-55 11509323 - Am J Respir Cell Mol Biol. 2001 Aug;25(2):150-5 15175330 - J Biol Chem. 2004 Aug 6;279(32):33409-12 |
References_xml | – volume: 25 start-page: 159 issue: 2 year: 2005 end-page: 161 ident: CR3 article-title: Temporal expression of Notch in preterm rat lungs exposed to hyperoxia publication-title: J Huazhong. Univ Sci Technol [Med Sci] – volume: 70 start-page: 240 issue: 2 year: 2005 end-page: 245 ident: CR5 article-title: Bioenergetics and death publication-title: Biochemistry (Moscow) doi: 10.1007/s10541-005-0106-3 – volume: 279 start-page: 33409 year: 2004 end-page: 33412 ident: CR12 article-title: ATP synthase that lacks F a-subunit publication-title: J Biol Chem doi: 10.1074/jbc.M404993200 – volume: 1 start-page: 02 issue: 4 year: 2005 end-page: 13 ident: CR11 article-title: A biophysical model of the mitochondrial respiratory system and oxidative phosphorylation publication-title: Plos Comput Biol doi: 10.1371/journal.pcbi.0010036 – volume: 5 start-page: 427 issue: 10 year: 2007 end-page: 429 ident: CR6 article-title: Relationship between mitochondrial electron transport chain dysfunction, development, and life extension in Caenorhabditis elegans publication-title: Plos Biol doi: 10.1371/journal.pbio.0050259 – volume: 22 start-page: 241 issue: 4 year: 2007 end-page: 243 ident: CR4 article-title: Diagnosis and treatment of neonatal bronchopulmonary dysplasia publication-title: Chin J Pract Pediatr (Chinese) – volume: 103 start-page: 13045 issue: 35 year: 2006 end-page: 13050 ident: CR10 article-title: Surface-modulated motion switch: capture and release of iron-sulfur protein in the cytochrome bc1 complex publication-title: Proc Natl Acacl Sci doi: 10.1073/pnas.0601149103 – volume: 4 start-page: 346 issue: 2 year: 2005 end-page: 355 ident: CR7 article-title: Functional Analysis of subunit e of the F F -ATPase of the yeast saccharomyces cerevisiave: Importance of the N-Terminal membrane anchor region publication-title: Eukaryot Cell doi: 10.1128/EC.4.2.346-355.2005 – volume: 50 start-page: 834 issue: 6 year: 2007 end-page: 847 ident: CR14 article-title: Microarray analysis of oxidative stress regulated genes mesencephalic dopaminergic neuronal cells: Relevance oxidative damage in Parkinson’ s disease publication-title: Neurochem Int doi: 10.1016/j.neuint.2007.02.003 – volume: 86 start-page: 1332 issue: 3 year: 2004 end-page: 13344 ident: CR8 article-title: Insights into the molecular mechanism of rotation in the F sector of ATP synthase publication-title: Biophys J doi: 10.1016/S0006-3495(04)74205-8 – volume: 8 start-page: 1 issue: 1 year: 2007 end-page: 9 ident: CR13 article-title: Azithromycin in the extremely low birth weight infant for the prevention of Bronchopulmonary Dysplasia: a pilot study publication-title: Respir Res doi: 10.1186/1465-9921-8-41 – volume: 25 start-page: 150 issue: 2 year: 2001 end-page: 155 ident: CR1 article-title: Apoptosis in neonatal murine lung exposed to hyperoia publication-title: Am J Respir Cell Mol Biol – volume: 6 start-page: 8 year: 2006 ident: CR2 article-title: Spatial and temporal expression of surfactant proteins in hyperoxia-induced neonatal rat lung injury publication-title: BMC Pulm Med doi: 10.1186/1471-2466-6-8 – volume: 14 start-page: 23 issue: 20 year: 2004 end-page: 27 ident: CR9 article-title: Study on changes of mitochondrial DNA ATPase6, 8 genes of small intestine epithelial cells in ischemia-reperfusion rats publication-title: Chin J Mod Med – volume: 8 start-page: 1 issue: 1 year: 2007 ident: 224_CR13 publication-title: Respir Res doi: 10.1186/1465-9921-8-41 – volume: 86 start-page: 1332 issue: 3 year: 2004 ident: 224_CR8 publication-title: Biophys J doi: 10.1016/S0006-3495(04)74205-8 – volume: 5 start-page: 427 issue: 10 year: 2007 ident: 224_CR6 publication-title: Plos Biol – volume: 22 start-page: 241 issue: 4 year: 2007 ident: 224_CR4 publication-title: Chin J Pract Pediatr (Chinese) – volume: 6 start-page: 8 year: 2006 ident: 224_CR2 publication-title: BMC Pulm Med doi: 10.1186/1471-2466-6-8 – volume: 279 start-page: 33409 year: 2004 ident: 224_CR12 publication-title: J Biol Chem doi: 10.1074/jbc.M404993200 – volume: 50 start-page: 834 issue: 6 year: 2007 ident: 224_CR14 publication-title: Neurochem Int doi: 10.1016/j.neuint.2007.02.003 – volume: 25 start-page: 150 issue: 2 year: 2001 ident: 224_CR1 publication-title: Am J Respir Cell Mol Biol doi: 10.1165/ajrcmb.25.2.4362 – volume: 4 start-page: 346 issue: 2 year: 2005 ident: 224_CR7 publication-title: Eukaryot Cell doi: 10.1128/EC.4.2.346-355.2005 – volume: 103 start-page: 13045 issue: 35 year: 2006 ident: 224_CR10 publication-title: Proc Natl Acacl Sci doi: 10.1073/pnas.0601149103 – volume: 70 start-page: 240 issue: 2 year: 2005 ident: 224_CR5 publication-title: Biochemistry (Moscow) doi: 10.1007/s10541-005-0106-3 – volume: 25 start-page: 159 issue: 2 year: 2005 ident: 224_CR3 publication-title: J Huazhong. Univ Sci Technol [Med Sci] doi: 10.1007/BF02873565 – volume: 14 start-page: 23 issue: 20 year: 2004 ident: 224_CR9 publication-title: Chin J Mod Med – volume: 1 start-page: 02 issue: 4 year: 2005 ident: 224_CR11 publication-title: Plos Comput Biol doi: 10.1371/journal.pcbi.0010036 – reference: 16924113 - Proc Natl Acad Sci U S A. 2006 Aug 29;103(35):13045-50 – reference: 17397968 - Neurochem Int. 2007 May;50(6):834-47 – reference: 17914900 - PLoS Biol. 2007 Oct 2;5(10):e259 – reference: 11509323 - Am J Respir Cell Mol Biol. 2001 Aug;25(2):150-5 – reference: 16116961 - J Huazhong Univ Sci Technolog Med Sci. 2005;25(2):159-61, 165 – reference: 14990464 - Biophys J. 2004 Mar;86(3):1332-44 – reference: 15701797 - Eukaryot Cell. 2005 Feb;4(2):346-55 – reference: 15175330 - J Biol Chem. 2004 Aug 6;279(32):33409-12 – reference: 16620381 - BMC Pulm Med. 2006 Apr 18;6:8 – reference: 15807664 - Biochemistry (Mosc). 2005 Feb;70(2):240-5 – reference: 17550598 - Respir Res. 2007 Jun 05;8:41 – reference: 16163394 - PLoS Comput Biol. 2005 Sep;1(4):e36 |
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Snippet | To investigate the effects of hyperoxia on mitochondrial multienzyme complex Ⅲ (cytochrome, Cytb) and Ⅴ (ATPase6, 8) in premature newborn rat lung, the... Summary To investigate the effects of hyperoxia on mitochondrial multienzyme complex III (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung,... To investigate the effects of hyperoxia on mitochondrial multienzyme complex III (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the... R3; To investigate the effects of hyperoxia on mitochondrial multienzyme complex Ⅲ (cytochrome, Cytb) and V (ATPase6, 8) in premature newborn rat lung, the... |
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SubjectTerms | Animals Animals, Newborn Cytochromes b - metabolism Electron Transport Complex III - metabolism Electron Transport Complex IV - metabolism Female Hyperoxia - metabolism Lung - metabolism Lung - pathology Male Medicine Medicine & Public Health Mitochondria - metabolism Models, Biological Multienzyme Complexes - metabolism Oxygen - metabolism Rats Rats, Sprague-Dawley 呼吸系统 多酶复合物 |
Title | Effects of Hyperoxia on Mitochondrial Multienzyme Complex Ⅲ and Ⅴ in Premature Newborn Rat Lung |
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