Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Iriny Ayoub
  • Marawan A. Elbaset
  • Mai M. Elghonemy
  • samir bashandy
  • Fatma A. A. Ibrahim
  • Omar Ahmed-Farid
  • Abdel Nasser Elgendy
  • Sherif M. Afifi
  • Tuba Esatbeyoglu
  • Abdel Razik H. Farrag
  • mohamed farag
  • Abdelsamed Elshamy

Externe Organisationen

  • Ain Shams University
  • National Research Center, Cairo
  • National Research Centre (NRC)
  • National Organization for Drug Control and Research, Cairo
  • University of Sadat City
  • Cairo University
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Aufsatznummer6470
FachzeitschriftMolecules
Jahrgang27
Ausgabenummer19
PublikationsstatusVeröffentlicht - Okt. 2022

Abstract

Cyperus species represent a group of cosmopolitan plants used in folk medicine to treat several diseases. In the current study, the phytochemical profile of Cyperus laevigatus ethanolic extract (CLEE) was assessed using UPLC-QTOF–MS/MS. The protective effect of CLEE at 50 and 100 mg /kg body weight (b.w.) was evaluated on hepatorenal injuries induced by thioacetamide (100 mg/kg) via investigation of the extract’s effects on oxidative stress, inflammatory markers and histopathological changes in the liver and kidney. UPLC-QTOF–MS/MS analysis of CLEE resulted in the identification of 94 compounds, including organic and phenolic acids, flavones, aurones, and fatty acids. CLEE improved the antioxidant status in the liver and kidney, as manifested by enhancement of reduced glutathione (GSH) and coenzyme Q10 (CoQ10), in addition to the reduction in malondialdehyde (MDA), nitric oxide (NO), and 8-hydroxy-2′-deoxyguanosine (8OHdG). Moreover, CLEE positively affected oxidative stress parameters in plasma and thwarted the depletion of hepatorenal ATP content by thioacetamide (TAA). Furthermore, treatment of rats with CLEE alleviated the significant increase in plasma liver enzymes, kidney function parameters, and inflammatory markers. The protective effect of CLEE was confirmed by a histopathological study of the liver and kidney. Our results proposed that CLEE may reduce TAA-hepatorenal toxicity via its antioxidant and anti-inflammatory properties suppressing oxidative stress.

ASJC Scopus Sachgebiete

Zitieren

Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats. / Ayoub, Iriny; Elbaset, Marawan A.; Elghonemy, Mai M. et al.
in: Molecules, Jahrgang 27, Nr. 19, 6470, 10.2022.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Ayoub, I, Elbaset, MA, Elghonemy, MM, bashandy, S, Ibrahim, FAA, Ahmed-Farid, O, Elgendy, AN, Afifi, SM, Esatbeyoglu, T, Farrag, ARH, farag, M & Elshamy, A 2022, 'Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats', Molecules, Jg. 27, Nr. 19, 6470. https://doi.org/10.3390/molecules27196470
Ayoub, I., Elbaset, M. A., Elghonemy, M. M., bashandy, S., Ibrahim, F. A. A., Ahmed-Farid, O., Elgendy, A. N., Afifi, S. M., Esatbeyoglu, T., Farrag, A. R. H., farag, M., & Elshamy, A. (2022). Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats. Molecules, 27(19), Artikel 6470. https://doi.org/10.3390/molecules27196470
Ayoub I, Elbaset MA, Elghonemy MM, bashandy S, Ibrahim FAA, Ahmed-Farid O et al. Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats. Molecules. 2022 Okt;27(19):6470. doi: 10.3390/molecules27196470
Ayoub, Iriny ; Elbaset, Marawan A. ; Elghonemy, Mai M. et al. / Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats. in: Molecules. 2022 ; Jahrgang 27, Nr. 19.
Download
@article{ae33c57adf8a41309b58b18638e3156c,
title = "Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats",
abstract = "Cyperus species represent a group of cosmopolitan plants used in folk medicine to treat several diseases. In the current study, the phytochemical profile of Cyperus laevigatus ethanolic extract (CLEE) was assessed using UPLC-QTOF–MS/MS. The protective effect of CLEE at 50 and 100 mg /kg body weight (b.w.) was evaluated on hepatorenal injuries induced by thioacetamide (100 mg/kg) via investigation of the extract{\textquoteright}s effects on oxidative stress, inflammatory markers and histopathological changes in the liver and kidney. UPLC-QTOF–MS/MS analysis of CLEE resulted in the identification of 94 compounds, including organic and phenolic acids, flavones, aurones, and fatty acids. CLEE improved the antioxidant status in the liver and kidney, as manifested by enhancement of reduced glutathione (GSH) and coenzyme Q10 (CoQ10), in addition to the reduction in malondialdehyde (MDA), nitric oxide (NO), and 8-hydroxy-2′-deoxyguanosine (8OHdG). Moreover, CLEE positively affected oxidative stress parameters in plasma and thwarted the depletion of hepatorenal ATP content by thioacetamide (TAA). Furthermore, treatment of rats with CLEE alleviated the significant increase in plasma liver enzymes, kidney function parameters, and inflammatory markers. The protective effect of CLEE was confirmed by a histopathological study of the liver and kidney. Our results proposed that CLEE may reduce TAA-hepatorenal toxicity via its antioxidant and anti-inflammatory properties suppressing oxidative stress.",
keywords = "aurones, flavonoids, hepatorenal injuries, histopathology, inflammation markers, oxidative stress, smooth flatsedge",
author = "Iriny Ayoub and Elbaset, {Marawan A.} and Elghonemy, {Mai M.} and samir bashandy and Ibrahim, {Fatma A. A.} and Omar Ahmed-Farid and Elgendy, {Abdel Nasser} and Afifi, {Sherif M.} and Tuba Esatbeyoglu and Farrag, {Abdel Razik H.} and mohamed farag and Abdelsamed Elshamy",
note = "Funding Information: The publication of this article was funded by the Open Access Fund of Leibniz Universit{\"a}t Hannover.",
year = "2022",
month = oct,
doi = "10.3390/molecules27196470",
language = "English",
volume = "27",
journal = "Molecules",
issn = "1420-3049",
publisher = "Multidisciplinary Digital Publishing Institute",
number = "19",

}

Download

TY - JOUR

T1 - Chemical Profile of Cyperus laevigatus and Its Protective Effects against Thioacetamide-Induced Hepatorenal Toxicity in Rats

AU - Ayoub, Iriny

AU - Elbaset, Marawan A.

AU - Elghonemy, Mai M.

AU - bashandy, samir

AU - Ibrahim, Fatma A. A.

AU - Ahmed-Farid, Omar

AU - Elgendy, Abdel Nasser

AU - Afifi, Sherif M.

AU - Esatbeyoglu, Tuba

AU - Farrag, Abdel Razik H.

AU - farag, mohamed

AU - Elshamy, Abdelsamed

N1 - Funding Information: The publication of this article was funded by the Open Access Fund of Leibniz Universität Hannover.

PY - 2022/10

Y1 - 2022/10

N2 - Cyperus species represent a group of cosmopolitan plants used in folk medicine to treat several diseases. In the current study, the phytochemical profile of Cyperus laevigatus ethanolic extract (CLEE) was assessed using UPLC-QTOF–MS/MS. The protective effect of CLEE at 50 and 100 mg /kg body weight (b.w.) was evaluated on hepatorenal injuries induced by thioacetamide (100 mg/kg) via investigation of the extract’s effects on oxidative stress, inflammatory markers and histopathological changes in the liver and kidney. UPLC-QTOF–MS/MS analysis of CLEE resulted in the identification of 94 compounds, including organic and phenolic acids, flavones, aurones, and fatty acids. CLEE improved the antioxidant status in the liver and kidney, as manifested by enhancement of reduced glutathione (GSH) and coenzyme Q10 (CoQ10), in addition to the reduction in malondialdehyde (MDA), nitric oxide (NO), and 8-hydroxy-2′-deoxyguanosine (8OHdG). Moreover, CLEE positively affected oxidative stress parameters in plasma and thwarted the depletion of hepatorenal ATP content by thioacetamide (TAA). Furthermore, treatment of rats with CLEE alleviated the significant increase in plasma liver enzymes, kidney function parameters, and inflammatory markers. The protective effect of CLEE was confirmed by a histopathological study of the liver and kidney. Our results proposed that CLEE may reduce TAA-hepatorenal toxicity via its antioxidant and anti-inflammatory properties suppressing oxidative stress.

AB - Cyperus species represent a group of cosmopolitan plants used in folk medicine to treat several diseases. In the current study, the phytochemical profile of Cyperus laevigatus ethanolic extract (CLEE) was assessed using UPLC-QTOF–MS/MS. The protective effect of CLEE at 50 and 100 mg /kg body weight (b.w.) was evaluated on hepatorenal injuries induced by thioacetamide (100 mg/kg) via investigation of the extract’s effects on oxidative stress, inflammatory markers and histopathological changes in the liver and kidney. UPLC-QTOF–MS/MS analysis of CLEE resulted in the identification of 94 compounds, including organic and phenolic acids, flavones, aurones, and fatty acids. CLEE improved the antioxidant status in the liver and kidney, as manifested by enhancement of reduced glutathione (GSH) and coenzyme Q10 (CoQ10), in addition to the reduction in malondialdehyde (MDA), nitric oxide (NO), and 8-hydroxy-2′-deoxyguanosine (8OHdG). Moreover, CLEE positively affected oxidative stress parameters in plasma and thwarted the depletion of hepatorenal ATP content by thioacetamide (TAA). Furthermore, treatment of rats with CLEE alleviated the significant increase in plasma liver enzymes, kidney function parameters, and inflammatory markers. The protective effect of CLEE was confirmed by a histopathological study of the liver and kidney. Our results proposed that CLEE may reduce TAA-hepatorenal toxicity via its antioxidant and anti-inflammatory properties suppressing oxidative stress.

KW - aurones

KW - flavonoids

KW - hepatorenal injuries

KW - histopathology

KW - inflammation markers

KW - oxidative stress

KW - smooth flatsedge

UR - http://www.scopus.com/inward/record.url?scp=85139813049&partnerID=8YFLogxK

U2 - 10.3390/molecules27196470

DO - 10.3390/molecules27196470

M3 - Article

VL - 27

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 19

M1 - 6470

ER -