In current scientific article, rat liver mitochondria respond to the flavonoids dihydroquercetin (20–100 µM), 1-(2´-bromo-4´,5´-dimethoxyphenyl)-6,7-dimethoxy-1,2,3,4 for respiratory and processes of oxidative phosphorylation - tetrahydroisoquinolines F-18 (20-100 μM) and synthesized on the basis of followings 2-(3,4-dihydroxyphenyl)-6-[1-(2'-bromo-4',5'-dimethoxyphenyl)-6,7- The effect of dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl]methyl-3,5,7-trihydroxychroman-4-on the concentrations of the DHQ-11 conjugate (20-100 μM) was investigated in in vitro experiments. Experiments were conducted within 180-200 gram infertile white male rats. Mitochondrias from rat liver were isolated by the way of differential centrifugation. Concentrations of dihydroquercetin flavonoid 20, 60, 100 μM in FAD-dependent succinate oxidation in rat liver mitochondria were identified to be reliable respiratory control parameters and partially increased ADF/O value, the respiratory control coefficient as Chans demonstrated an increase in respiratory rate under the influence of the alkaloid F-18 isoquinoline 20, 60, 100 μM. Moreover, the ADP/O coefficients also boosted under the influence of the isoquinoline alkaloid F-18. It was observed that ADP/O ratio coefficients was expanded within the bonding by the effect of the DHQ-11 conjugate concentration. The concentration of 100 μM dihydroquercetin for FAD-dependent succinate oxidation in rat liver mitochondria surged Chance's respiratory rate by 15% compared to the control. Concentrations of isoquinoline alkaloid F-18 100 μM enlarged the respiratory rate by 13% compared to the control. It was defined that concentrations of 100 μM DHQ-11 conjugate rose the respiratory rate by 20%. The oxidation of FAD-dependent substrates in mitochondria was more actively effected by the DHQ-11 conjugate than dihydroquercetin and F-18 isoquinoline alkaloids.
Published in | American Journal of Biomedical and Life Sciences (Volume 10, Issue 3) |
DOI | 10.11648/j.ajbls.20221003.12 |
Page(s) | 65-69 |
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2022. Published by Science Publishing Group |
Liver, Mitochondria, FAD, ROS, Succinate, Dihydroquercetin, F-18 Isoquinoline Alkaloid, DHQ-11 Conjugate
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APA Style
Ernazarov Zafarjon Mamurovich, Pozilov Mamurjon Komiljonovich, Toshmatova Shoiraxon Ruziyevna, Zhurakulov Sherzod Niyatkobulovich. (2022). Influence of Dihydroquercetin, 1-Aryltetrahydroisoquinoline (F-18) and Their Conjugate (DHQ-11) on Mitochondrial Respiration and Oxidative Phosphorylation. American Journal of Biomedical and Life Sciences, 10(3), 65-69. https://doi.org/10.11648/j.ajbls.20221003.12
ACS Style
Ernazarov Zafarjon Mamurovich; Pozilov Mamurjon Komiljonovich; Toshmatova Shoiraxon Ruziyevna; Zhurakulov Sherzod Niyatkobulovich. Influence of Dihydroquercetin, 1-Aryltetrahydroisoquinoline (F-18) and Their Conjugate (DHQ-11) on Mitochondrial Respiration and Oxidative Phosphorylation. Am. J. Biomed. Life Sci. 2022, 10(3), 65-69. doi: 10.11648/j.ajbls.20221003.12
AMA Style
Ernazarov Zafarjon Mamurovich, Pozilov Mamurjon Komiljonovich, Toshmatova Shoiraxon Ruziyevna, Zhurakulov Sherzod Niyatkobulovich. Influence of Dihydroquercetin, 1-Aryltetrahydroisoquinoline (F-18) and Their Conjugate (DHQ-11) on Mitochondrial Respiration and Oxidative Phosphorylation. Am J Biomed Life Sci. 2022;10(3):65-69. doi: 10.11648/j.ajbls.20221003.12
@article{10.11648/j.ajbls.20221003.12, author = {Ernazarov Zafarjon Mamurovich and Pozilov Mamurjon Komiljonovich and Toshmatova Shoiraxon Ruziyevna and Zhurakulov Sherzod Niyatkobulovich}, title = {Influence of Dihydroquercetin, 1-Aryltetrahydroisoquinoline (F-18) and Their Conjugate (DHQ-11) on Mitochondrial Respiration and Oxidative Phosphorylation}, journal = {American Journal of Biomedical and Life Sciences}, volume = {10}, number = {3}, pages = {65-69}, doi = {10.11648/j.ajbls.20221003.12}, url = {https://doi.org/10.11648/j.ajbls.20221003.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajbls.20221003.12}, abstract = {In current scientific article, rat liver mitochondria respond to the flavonoids dihydroquercetin (20–100 µM), 1-(2´-bromo-4´,5´-dimethoxyphenyl)-6,7-dimethoxy-1,2,3,4 for respiratory and processes of oxidative phosphorylation - tetrahydroisoquinolines F-18 (20-100 μM) and synthesized on the basis of followings 2-(3,4-dihydroxyphenyl)-6-[1-(2'-bromo-4',5'-dimethoxyphenyl)-6,7- The effect of dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl]methyl-3,5,7-trihydroxychroman-4-on the concentrations of the DHQ-11 conjugate (20-100 μM) was investigated in in vitro experiments. Experiments were conducted within 180-200 gram infertile white male rats. Mitochondrias from rat liver were isolated by the way of differential centrifugation. Concentrations of dihydroquercetin flavonoid 20, 60, 100 μM in FAD-dependent succinate oxidation in rat liver mitochondria were identified to be reliable respiratory control parameters and partially increased ADF/O value, the respiratory control coefficient as Chans demonstrated an increase in respiratory rate under the influence of the alkaloid F-18 isoquinoline 20, 60, 100 μM. Moreover, the ADP/O coefficients also boosted under the influence of the isoquinoline alkaloid F-18. It was observed that ADP/O ratio coefficients was expanded within the bonding by the effect of the DHQ-11 conjugate concentration. The concentration of 100 μM dihydroquercetin for FAD-dependent succinate oxidation in rat liver mitochondria surged Chance's respiratory rate by 15% compared to the control. Concentrations of isoquinoline alkaloid F-18 100 μM enlarged the respiratory rate by 13% compared to the control. It was defined that concentrations of 100 μM DHQ-11 conjugate rose the respiratory rate by 20%. The oxidation of FAD-dependent substrates in mitochondria was more actively effected by the DHQ-11 conjugate than dihydroquercetin and F-18 isoquinoline alkaloids.}, year = {2022} }
TY - JOUR T1 - Influence of Dihydroquercetin, 1-Aryltetrahydroisoquinoline (F-18) and Their Conjugate (DHQ-11) on Mitochondrial Respiration and Oxidative Phosphorylation AU - Ernazarov Zafarjon Mamurovich AU - Pozilov Mamurjon Komiljonovich AU - Toshmatova Shoiraxon Ruziyevna AU - Zhurakulov Sherzod Niyatkobulovich Y1 - 2022/05/24 PY - 2022 N1 - https://doi.org/10.11648/j.ajbls.20221003.12 DO - 10.11648/j.ajbls.20221003.12 T2 - American Journal of Biomedical and Life Sciences JF - American Journal of Biomedical and Life Sciences JO - American Journal of Biomedical and Life Sciences SP - 65 EP - 69 PB - Science Publishing Group SN - 2330-880X UR - https://doi.org/10.11648/j.ajbls.20221003.12 AB - In current scientific article, rat liver mitochondria respond to the flavonoids dihydroquercetin (20–100 µM), 1-(2´-bromo-4´,5´-dimethoxyphenyl)-6,7-dimethoxy-1,2,3,4 for respiratory and processes of oxidative phosphorylation - tetrahydroisoquinolines F-18 (20-100 μM) and synthesized on the basis of followings 2-(3,4-dihydroxyphenyl)-6-[1-(2'-bromo-4',5'-dimethoxyphenyl)-6,7- The effect of dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl]methyl-3,5,7-trihydroxychroman-4-on the concentrations of the DHQ-11 conjugate (20-100 μM) was investigated in in vitro experiments. Experiments were conducted within 180-200 gram infertile white male rats. Mitochondrias from rat liver were isolated by the way of differential centrifugation. Concentrations of dihydroquercetin flavonoid 20, 60, 100 μM in FAD-dependent succinate oxidation in rat liver mitochondria were identified to be reliable respiratory control parameters and partially increased ADF/O value, the respiratory control coefficient as Chans demonstrated an increase in respiratory rate under the influence of the alkaloid F-18 isoquinoline 20, 60, 100 μM. Moreover, the ADP/O coefficients also boosted under the influence of the isoquinoline alkaloid F-18. It was observed that ADP/O ratio coefficients was expanded within the bonding by the effect of the DHQ-11 conjugate concentration. The concentration of 100 μM dihydroquercetin for FAD-dependent succinate oxidation in rat liver mitochondria surged Chance's respiratory rate by 15% compared to the control. Concentrations of isoquinoline alkaloid F-18 100 μM enlarged the respiratory rate by 13% compared to the control. It was defined that concentrations of 100 μM DHQ-11 conjugate rose the respiratory rate by 20%. The oxidation of FAD-dependent substrates in mitochondria was more actively effected by the DHQ-11 conjugate than dihydroquercetin and F-18 isoquinoline alkaloids. VL - 10 IS - 3 ER -