Effect of Polyphenols Isolated from Plantago major L. and Plantago lanceolata L. on Mitochondrial Permeability Transition Pore in Rat Liver

Authors

  • Nurali Ergashev Institute of Biophysics and Biochemistry at the National University of Uzbekistan, Tashkent, Republic of Uzbekistan
  • Khamida Sayfieva Alfraganus university, Tashkent, Republic of Uzbekistan
  • Rustam Makhmudov Institute of Bioorganic Chemistry, Academy of Sciences of the Republic of Uzbekistan, Tashkent, Republic of Uzbekistan
  • Muzaffar Asrarov Institute of Biophysics and Biochemistry at the National University of Uzbekistan, Tashkent, Republic of Uzbekistan

DOI:

https://doi.org/10.48048/tis.2024.7661

Keywords:

Mitochondria, Polyphenols, Malondialdehyde, Mitochondrial permeability transition pore

Abstract

It has been shown that the transport of electrons in the respiratory chain of mitochondria, ion-transport processes, the balance of Ca2+ ions and other metabolic processes in the cell are intrinsically connected with lipoperoxidation processes. In particular, in recent years, plant biologically active compounds have been widely used to eliminate oxidative processes developing in the body. Accordingly, we considered it important to study the mechanisms of action of xylopyr-T, glucopyr-T and 2-DVG polyphenols isolated from the plants Plantago major L. and Plantago lanceolata L., belonging to the Plantaginaceae family, which are widely used in folk medicine. Therefore, in vitro experiments, the amount of malondialdehyde and the condition state of mPTP were studied by spectrophotometric method. The obtained results revealed that the studied polyphenols inhibit lipoperoxidation induced by Fe2+/ascorbate the production of malondialdehyde was reduce by xylopyr-T to 81.9 ± 1.2 %, by glucopyr-T to 79.4 ± 1.7 % and by 2-DVG to 75.0 ± 1.8 % at a concentration of 4 µM in rat liver mitochondria. At the same time, mPTP opening in the medium with the substrate succinate (+ rotenone) inhibition 2-DVG polyphenol at a concentration of 100 μM was reduced by 84.5 ± 2.8 %, xylopyr-T polyphenol at a concentration of 200 μM by 67.6 ± 4.8 % and it was shown that glucopyr-T polyphenol at a concentration of 200 µM by 32.5 ± 1.65 % compared to the control. In conclusion, it can be illustrated that the studied polyphenols, along with their high antioxidant properties, show a structure-dependent inhibition of mPTP opening, which is involved in various physiological and pathological processes.

HIGHLIGHTS  

  • In this study, hydrolysable tannins, which have strong antioxidant properties isolated from Plantago plants, were investigated and confirmed by MDA analysis in vitro
  • These hydrolyzable tannins exhibited substrate-dependent inhibition of rat liver mitochondrial PTP in vitro
  • It can be assumed from the data obtained that these hydrolyzable tannins act organ-specifically

GRAPHICAL ABSTRACT 

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

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.

C Rogers, B Davis, PD Neufer, MP Murphy, EJ Anderson and J Robidoux. A transient increase in lipid peroxidation primes preadipocytes for delayed mitochondrial inner membrane permeabilization and ATP depletion during prolonged exposure to fatty acids. Free Radic. Biol. Med. 2014; 67, 330-41.

C Mammucari, A Raffaello, DV Reane, G Gherardi, AD Mario and R Rizzuto. Mitochondrial calcium uptake in organ physiology: From molecular mechanism to animal models. Pflügers Arch. 2018; 470, 1165-79.

L Modesti, A Danese, VAM Vitto, D Ramaccini, G Aguiari, R Gafà, G Lanza, C Giorgi and P Pinton. Mitochondrial Ca2+ signaling in health, disease and therapy. Cells 2021; 10, 1317.

M Bonora, C Giorgi and P Pinton. Molecular mechanisms and consequences of mitochondrial permeability transition. Nat. Rev. Mol. Cell Biol. 2022; 23, 266-85.

P Bernardi, C Gerle, AP Halestrap, EA Jonas, J Karch, N Mnatsakanyan, E Pavlov, SS Sheu and AA Soukas. Identity, structure, and function of the mitochondrial permeability transition pore: Controversies, consensus, recent advances, and future directions. Cell Death Differ. 2023; 30, 1869-85.

MA Neginskaya, ME Solesio, EV Berezhnaya, GF Amodeo, N Mnatsakanyan, EA Jonas and EV Pavlov. ATP synthase C-subunit-deficient mitochondria have a small cyclosporine a-sensitive channel, but lack the permeability transition pore. Cell Rep. 2019; 26, 11-17.e2.

T Umegaki, Y Okimura, H Fujita, H Yano, J Akiyama, M Inoue, K Utsumi and J Sasaki. Flow cytometric analysis of ca-induced membrane permeability transition of isolated rat liver mitochondria. J. Clin. Biochem. Nutr. 2008; 42, 35-44.

T Briston, DL Selwood, G Szabadkai and MR Duchen. Mitochondrial permeability transition: A molecular lesion with multiple drug targets. Trends Pharmacol. Sci. 2019; 40, 50-70.

RR Makhmudov, NG Abdulladzhanova and FG Kamaev. Phenolic compounds from Plantago major and P. Lanceolata. Chem. Nat. Comp. 2011; 47, 288-9.

WC Schneider and GH Hogeboom. Cytochemical studies of mammalian tissues: The isolation of cell components by differential centrifugation. Canc. Res. 1951; 11, 1-22.

C Watters. A one-step biuret assay for protein in the presence of detergent. Anal. Biochem. 1978; 88, 695-8.

ID Stalnaya and TG Garishvili. Method of evaluation of malondialdehyde with thiobarbituric acid. In: VN Orekhovich (Ed.). Modern methods in biochemistry. Medicine, Moscow, Russia, 1977, p. 66-8.

L He and JJ Lemasters. Regulated and unregulated mitochondrial permeability transition pores: A new paradigm of pore structure and function. FEBS Lett. 2002; 512, 1-7.

R Abeti, MH Parkinson, IP Hargreaves, PR Angelova, C Sandi, MA Pook, P Giunti and AY Abramov. Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich’s ataxia. Cell Death Dis. 2016; 7, e2237.

F Basit, LMV Oppen, L Schöckel, HM Bossenbroek, SEVED Vries, JC Hermeling, S Grefte, C Kopitz, M Heroult, PH Willems and WJ Koopman. Mitochondrial complex I inhibition triggers a mitophagy-dependent ROS increase leading to necroptosis and ferroptosis in melanoma cells. Cell Death Dis. 2017; 8, e2716.

MI Asrarov, EJ Komilov, NA Ergashev, MK Pozilov, KA Eshbakova, ZA Toshmatov and MX Tashbekova. The mechanism of action of flavone luteolin on the function of rat liver mitochondria. Problem Biol. Med. Pharm. Chem. 2015; 12, 38-43.

W Bors and C Michel. Chemistry of the antioxidant effect of polyphenols. Ann. New York Acad. Sci. 2002; 957, 57-69.

UG Gayibov, EJ Komilov, RN Rakhimov, NA Ergashev, NG Abdullajanova, MI Asrorov and TF Aripov. Influence of new polyphenol compound from Euphorbia plant on mitochondrial function. J. Microbiol. Biotechnol. Food Sci. 2019; 8, 1021-5.

T Briston, M Roberts, S Lewis, B Powney, JM Staddon, G Szabadkai and MR Duchen. Mitochondrial permeability transition pore: Sensitivity to opening and mechanistic dependence on substrate availability. Sci. Rep. 2017; 7, 10492.

KJ Sayfieva, NA Ergashev, B Yuldoshev, EJ Komilov, RR Makhmudov and MI Asrarov. The effect of some tannins on the rat liver mitochondrial megapore. Univ. Chem. Biol. 2021; 5, 54-7.

KJ Sayfieva, NA Ergashev, EJ Komilov, RR Makhmudov and MI Asrarov. Regulation of the rat liver mitochondrial megapore by some polyphenolic compounds. Uzbek Biol. J. 2021; 2, 3-6.

KW Kinnally, PM Peixoto, SY Ryu and LM Dejean. Is mPTP the gatekeeper for necrosis, apoptosis, or both? Biochim. Biophys. Acta 2011; 1813, 616-22.

JN Weiss, P Korge, HM Honda and P Ping. Role of the mitochondrial permeability transition in myocardial disease. Circ. Res. 2003; 93, 292-301.

K Aoki, K Nishimura, H Abe, H Maruta, H Sakagami, T Hatano, T Okuda, T Yoshida, YJ Tsai, F Uchiumi and S Tanuma. Novel inhibitors of poly(ADP-ribose) glycohydrolase. Biochim. Biophys. Acta 1993; 1158, 251-6.

Downloads

Published

2024-04-20

How to Cite

Ergashev, N., Sayfieva, K., Makhmudov, R., & Asrarov, M. (2024). Effect of Polyphenols Isolated from Plantago major L. and Plantago lanceolata L. on Mitochondrial Permeability Transition Pore in Rat Liver. Trends in Sciences, 21(7), 7661. https://doi.org/10.48048/tis.2024.7661