Correction of the Mitochondrial NADH Oxidase Activity, Peroxidation and Phospholipid Metabolism by Haplogenin-7-Glucoside in Hypoxia and Ischemia

Authors

  • Yusupova Umidakhon Department of Human and Animal Physiology, National University of Uzbekistan named after Mirzo Ulugbek, Tashkent, Uzbekistan
  • Botirov Erkin Head of Chemistry Department, Surgut State University, Okrug, Russia
  • Gayibov Ulugbek Institute of Bioorganic Chemistry of the Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan
  • Niyazmetov Bahadir Department of Human and Animal Physiology, National University of Uzbekistan named after Mirzo Ulugbek, Tashkent, Uzbekistan
  • Almatov Karim Department of Human and Animal Physiology, National University of Uzbekistan named after Mirzo Ulugbek, Tashkent, Uzbekistan

DOI:

https://doi.org/10.48048/tis.2022.6260

Keywords:

Rotenone, NADH oxidase, Apoptosis, Hypoxia, Ischemia, Haplogenin-7-glucoside, Peroxidation of lipids (LPO), Phospholipids

Abstract

In this study, it was used haplogenin-7-glucoside flavonol (C16H12O8) isolated from the plant Haplophyllum perforatum. It was studied the effect of haplogenin-7-glycoside on NADH oxidase activity, peroxidation, and phospholipid metabolism in rat liver mitochondria under in vitro conditions. Incubation of mitochondria at 37 ℃ leads to disruption of the integrity of mitochondrial membranes, as a result, in cytochrome с desorption from the inner membrane into the intermembrane space, which leads to a decrease in the activity of rotenone-sensitive NADH oxidase and an increase in the activity of rotenone-insensitive NADH oxidase. Haplogenin-7-glucoside exhibits membrane stabilization by reducing these alterations. Under ischemia conditions, the effect of haplogenin-7-glucoside on the LPO process in mitochondria decreases LPO in mitochondria. Quantitative changes in phosphatidylserine in mitochondrial membranes under LPO conditions during incubation of mitochondria at 37 ℃ were observed to accelerate controlled (auto-oxidation) LPO over time (0 - 90 min). Peroxidation of phosphatidylserine in mitochondria when the addition of haplogenin-7-glucoside to the incubation medium at 30, 60 and 90 min, LPO was found to be reduced. The increasing amount of phosphatidylinositol has not happened depend on time. However, a slight increase was found under the influence of haplogenin-7-glucoside.

HIGHLIGHTS

  • Cytochrome c desorption from the inner membrane into the interstitial space leads to a decrease in the activity of rotenone-sensitive NADH-oxidase and an increase in the activity of non-rotenone-sensitive NADH-oxidase
  • Haplogenin-7-glycoside showed membrane-stabilizing properties by significantly reducing these changes; the addition of haplogenin-7-glucoside to mitochondria leads to a decrease for MDA, a decrease in the LPO process
  • At incubation of mitochondria at 37℃, the amount of phosphatidic acid and lysophosphatidic acid in mitochondria under LPO conditions was also found to be less than control under the influence of haplogenin-7-glucoside. Thus, haplogenin-7-glucoside reduces the rate of peroxidation of phospholipids in liver mitochondria and has a corrective effect

GRAPHICAL ABSTRACT

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

KT Almatov, UR Yusupova, GR Abdullayev, MM Mamajanov, SO Mirzakulov and BA Niyazmetov. Determining the body’s respiration and energy production. Tashkent, 2013, p. 103.

JJ Neher, JV Emmrich, M Fricker, PK Mander, C Théry and GC Brown. Phagocytosis executes delayed neuronal death after focal brain ischemia. Proc. Nat. Acad. 2013; 110, E4098-E4107.

A Pakiet, J Kobiela, P Stepnowski, T Sledzinski and A Mika. Changes in lipids composition and metabolism in colorectal cancer: A review. Lipids Health Dis. 2019; 18, 29.

YA Vladimirov. Biological membranes and unprogrammed cell death. Soros Educ. J. 2000; 6, 2-9.

YA Vladimirov and AM Archakov. Lipid peroxidation in biological membranes. Science, Moscow, Russia, 1972, p. 214.

LFS Silva, MD Brito, JMC Yuzawa and TR Rosenstock. Mitochondrial dysfunction and changes in high-energy compounds in different cellular models associated to hypoxia: Implication to schizophrenia. Sci. Rep. 2019; 9, 18049.

R Pluta, M Ułamek-Kozioł, S Januszewski and JS Czuczwar. Tau protein dysfunction after brain ischemia. J. Alzheimers Dis. 2018; 66, 429-37.

C Giorgi, S Marchi, ICM Simoes, Z Ren, G Morciano, M Perrone, P Patalas-Krawczyk, S Borchard, P Jędrak, K Pierzynowska, J Szymański, DQ Wang, P Portincasa, G Węgrzyn, H Zischka, P Dobrzyn, M Bonora, J Duszynski, A Rimessi, …, MR Wieckowski. Mitochondria and reactive oxygen species in aging and age-related diseases. Int. Rev. Cell Mol. Biol. 2018; 340, 209-344.

KN Belosludtsev, EY Talanov, VS Starinets, AV Agafonov, MV Dubinin and NV Belosludtseva. Transport of Ca2+ and Ca2+-dependent permeability transition in rat liver mitochondria under the streptozotocin-induced type I diabetes. Cells 2019; 8, 1014.

P Wójcik, A Gęgotek, N Žarković and E Skrzydlewska. Oxidative stress and lipid mediators modulate immune cell functions in autoimmune diseases. Int. J. Mol. Sci. 2021; 22, 723.

S Matsuzaki, PA Szweda, LI Szweda and KM Humphries. Regulated production of free radicals by the mitochondrial electron transport chain: Cardiac ischemic preconditioning. Adv. Drug Deliv. Rev. 2009; 61, 1324-31.

F Li, J Li, S Li, S Guo and P Li. Modulatory effects of Chinese herbal medicines on energy metabolism in ischemic heart diseases. Front. Pharmacol. 2020; 11, 995.

DC Fuhrmann and B Brüne. Mitochondrial composition and function under the control of hypoxia. Redox Biol. 2017; 12, 208-15.

J Šrámek, V Němcová-Fürstová and J Kovář. Molecular mechanisms of apoptosis induction and its regulation by fatty acids in pancreatic β-cells. Int. J. Mol. Sci. 2021; 22, 4285.

X Fan, J Du, MH Wang, JM Li, B Yang, Y Chen, JC Dai, C Zhang and J Zhou. Irisin contributes to the hepatoprotection of dexmedetomidine during intestinal ischemia/reperfusion. Oxid. Med. Cell. Longevity 2019; 2019, 7857082.

M Hendriks and SK Ramasamy. Blood vessels and vascular niches in bone development and physiological remodeling. Front. Cell Dev. Biol. 2020; 8, 602278.

RP Rustamova and KT Almatov. Regulation of the activity of lipolytic enzymes of mitochondria by apigenin. Vestnik NUUz 2011; 3, 22-4.

ML Contreras-Zentella and R Hernández-Muñoz. Is liver enzyme release really associated with cell necrosis induced by oxidant stress? Oxid. Med. Cell. Longevity 2016; 2016, 3529149.

J Kamarauskaite, R Baniene, D Trumbeckas, A Strazdauskas and S Trumbeckaite. Increased succinate accumulation induces ROS generation in in vivo ischemia/reperfusion-affected rat kidney mitochondria. Biomed. Res. Int. 2020; 2020: 8855585.

BK Chacko, A Srivastava, MS Johnson, GA Benavides, MJ Chang, Y Ye, N Jhala, MP Murphy, B Kalyanaraman and VM Darley-Usmar. The mitochondria-targeted ubiquinone MitoQ decreases ethanol-dependent micro and macro hepatosteatosis. Hepatology 2011; 54, 153-63.

MZ Noman, M Hasmim, Y Messai, S Terry, C Kieda, B Janji and S Chouaib. Hypoxia: A key player in antitumor immune response. A review in the theme: cellular responses to hypoxia. Am. J. Physiol. Cell Physiol. 2015; 309, C569-C579.

GM Otto, CL Franklin and CB Clifford. Chapter 4 - biology and diseases of rats. Lab. Anim. Med. 2015, DOI: 10.1016/B978-0-12-409527-4.00004-3.

AM Almeida, CRA Bertoncini, J Borecky, NC Souza-Pinto and AE Vercesi. Mitochondrial DNA damage associated with lipid peroxidation of the mitochondrial membrane induced by Fe2+-citrate. An. Acad. Bras. Ciênc. 2006; 78, 505-14.

EJ Anderson, LA Katunga and MS Willis. Mitochondria as a source and target of lipid peroxidation products in healthy and diseased heart. Clin. Exp. Pharmacol. Physiol. 2012; 39, 179-93.

VA Bohr, T Stevnsner and NC de Souza-Pinto. Mitochondrial DNA repair of oxidative damage in mammalian cells. Gene 2002; 286, 127-34.

EG Bligh and WJ Dyer. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 1959; 37, 911-7.

MK Chahar, N Sharma, MP Dobhal and YC Joshi. Flavonoids: A versatile source of anticancer drugs. Pharmacogn. Rev. 2011; 5, 1-12.

CK Petito, RP Kraig and WA Pulsinelli. Light and electron microscopic evaluation of hydrogen ion-induced brain necrosis. J. Cerebr. Blood Flow Metabol. 1987; 7, 625-32.

G Bozzuto and A Molinari. Liposomes as nanomedical devices. Int. J. Nanomedicine 2015; 10, 975-99.

J Dudek. Role of cardiolipin in mitochondrial signaling pathways. Front. Cell Dev. Biol. 2017; 5, 90.

MA Graziewicz, BJ Day and WC Copeland. The mitochondrial DNA polymerase as a target of oxidative damage. Nucleic Acids Res. 2002; 30, 2817-24.

J Mierziak, K Kostyn and A Kulma. Flavonoids as important molecules of plant interactions with the environment. Molecules 2014; 19, 16240-65.

Y He, J Liu, D Grossman, D Durrant, T Sweatman, L Lothstein, RF Epand, RM Epand and RM Lee. Phosphorylation of mitochondrial phospholipid scramblase 3 by protein kinase C-delta induces its activation and facilitates mitochondrial targeting of tBid. J. Cell. Biochem. 2007; 101, 1210-21.

CM Hebling, CR Morgan, DW Stafford, JW Jorgenson, KD Rand and JR Engen. Comformational analysis of membrane proteins in phospholipid bilayer nanodiscs by hydrogen exchange mass spectrometry. Anal. Chem. 2010; 82, 5415-9.

M Jannesar, MS Shoushtari, A Majd and Z Pourpak. Bee pollen flavonoids as a therapeutic agent in allergic and immunological disorders. Iranian J. Allergy Asthma Immunol. 2017; 16, 171-82.

RA Kikland, RM Adiphatla, JF Hatcher and JL Franklin. Loss of cardiolipin and mitochondria during programmed neuronal death: evidence of a role for lipid per oxidation and autophagy. Neuroscience 2002; 115, 587-602.

EB Kurutas. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: Current state. Nutr. J. 2015; 15, 71.

J Li, X Wang, T Zhang, C Wang, Z Huang, X Luo and Y Deng. A review on phospholipids and their main applications in drug delivery systems. Asian J. Pharmaceut. Sci. 2015; 10, 81-98.

G Huang, C Chu, T Huang, X Kong, Y Zhang, N Zhang and YD Cai. Exploring mouse protein function via multiple approaches. PLoS One 2016; 11, e0166580.

NA Brazhe, AB Evlyukhin, EA Goodilin, AA Semenova, SM Novikov, SI Bozhevolnyi, BN Chichkov, AS Sarycheva, AA Baizhumanov, EI Nikelshparg, LI Deev, EG Maksimov, GV Maksimov and O Sosnovtseva. Probing cytochrome c in living mitochondria with surface-enhanced Raman spectroscopy. Sci. Rep. 2015; 5, 13793.

LI Mennen, D Sapinho, H Ito, P Galan, S Hercberg and A Scalbert. Urinary excretion of 13 dietary flavonoids and phenolic acids in free-living healthy subjects - variability and possible use as biomarkers of polyphenol intake. Eur. J. Clin. Nutr. 2008; 62, 519-25

EJ Middleton, C Kandaswami and TC Theoharides. The effects of plant flavonoids on mammalian cells: Implications for inflammation, heart disase, and cancer. Pharmacol. Rev. 2000; 52, 673-751.

TA Leonard and JH Hurley. Regulation of protein kinases by lipids. Curr. Opin. Struct. Biol. 2011; 21, 785-91.

M Ott, JD Robertson, V Gogvadze, B Zhivotovsky and S Orrenius. Cytochrome c release from mitochondria proceeds by a two-step process. Proc. Nat. Acad. Sci. 2002; 99, 1259-63.

P Putta, J Rankenberg, RA Korver, R van Wijk, T Munnik, C Testerink and EE Kooijman. Phosphatidic acid binding proteins display differential binding as a function of membrane curvature stress and chemical properties. Biochim. Biophys. Acta Biomembr. 2016; 1858, 2709-16.

D Xu, MJ Hu, YQ Wang and YL Cui. Antioxidant activities of quercetin and its complexes for medicinal application. Molecules 2019; 24, 1123.

E Rosivatz and R Woscholski. Removal or masking of phosphatidylinositol(4,5)bisphosphate from the outer mitochondrial membrane causes mitochondrial fragmentation. Cell. Signal. 2011; 23, 478-86.

A Salaritabar, B Darvishi, F Hadjiakhoondi, A Manayi, A Sureda, SF Nabavi, LR Fitzpatrick, SM Nabavi and A Bishayee. Therapeutic potential of flavonoids in inflammatory bowel disease: A comprehensive review. World J. Gastroenterol. 2017; 23, 5097-114.

M Serafini, I Peluso and A Raguzzini. Flavonoids as anti-inflammatory agents. Proc. Nutr. Soc. 2010; 9, 273-8.

PC Liao , C Bergamini, R Fato, LA Pon and F Pallotti. Isolation of mitochondria from cells and tissues. Meth. Cell Biol. 2020; 155, 3-31.

F Ververidis, E Trantas, C Douglas, G Vollmer, G Kretzschmar and N Panopoulos. Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part I: Chemical diversity, impacts on plant biology and human health. Biotechnol. J. 2007; 2, 1214-34.

Downloads

Published

2022-10-17

How to Cite

Umidakhon, Y. ., Erkin, B. ., Ulugbek, G. ., Bahadir, N. ., & Karim, A. . (2022). Correction of the Mitochondrial NADH Oxidase Activity, Peroxidation and Phospholipid Metabolism by Haplogenin-7-Glucoside in Hypoxia and Ischemia. Trends in Sciences, 19(21), 6260. https://doi.org/10.48048/tis.2022.6260