Antitumor and hepatoprotective effect of Cuscuta reflexa Roxb. in a murine model of colon cancer.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
10 Jan 2022
Historique:
received: 22 05 2021
revised: 16 08 2021
accepted: 01 09 2021
pubmed: 8 9 2021
medline: 29 1 2022
entrez: 7 9 2021
Statut: ppublish

Résumé

Cuscuta reflexa Roxb. (C. reflexa) is a well-known traditional herbal plant, with numerous inherent therapeutic potentials including anticancer, antitumor, antibacterial, analgesic, anthelmintic, laxative and others. Moreover, the anticancer and antitumor potentials of this herb are ongoing with several trails, thus an attempt was made to assess the anticancer and hepatoprotective potentials of traditional C. reflexa herbs. The dried ethanolic extract of C. reflexa was tested for acute oral toxicity in the treated animals subsequently their behavioral, neurological, and autonomic profiles changes were observed. The preliminary anti-cancer effects of extracts against 1, 2- Dimethyl hydrazine (DMH) induced animals were assessed through barium enema X-ray, colonoscopy, and Aberrant crypt foci (ACF) studies. The blood samples of the animals (treated and untreated) were collected and their in-vitro histological parameters were evaluated by the experienced technician. It was observed that C. reflexa significantly reduced Disease activity indexing (DAI) level and ACF counting, as well as demonstrated similar activity as of the standard drug 5-Fluorouracil (5-FU). Histopathological results revealed that the apoptotic bodies decreased in the DMH-induced group (group II) during cancer progression while in 5-FU treated (group III) and C. reflexa treated (group IV and V) animals the apoptotic bodies were increased. Inversely, the mitotic bodies increased in group II animals and reduced in group III, IV, and V animals. In the colonic section, DMH-induced cancer assay exhibited significant effects on the levels of hemoglobin, Packed cell volume (PCV), Red blood cell (RBC) counts, Mean corpuscular hemoglobin concentration (MCHC), Mean corpuscular volume (MCV), and Mean cell hemoglobin (MCH), and was found to be less in group II animals whereas administration of C. reflexa efficiently recovered back the loss probably by healing the colon damage/depletion of cancer progression. Moreover, compared to the group II animals, the neutrophil count was within the normal range in C. reflexa administered group. In the present study, the major hematological parameters significantly increased within DMH treated animals and exhibited extensive damage in the hepatic regions. Moreover, the histopathological findings demonstrated that the C. reflexa extracts potentially reduced the cell proliferation, with no toxicity. The C. reflexa extracts exhibited impending anti-cancer activity as well as protected the hepatic cells and thus could be potentially used in the management of colon or colorectal cancer and hepatic impairments.

Identifiants

pubmed: 34492318
pii: S0378-8741(21)00826-6
doi: 10.1016/j.jep.2021.114597
pii:
doi:

Substances chimiques

Antineoplastic Agents, Phytogenic 0
Drugs, Chinese Herbal 0
Plant Extracts 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114597

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Shobhit Mishra (S)

Amity Institute of Pharmacy, Amity University, Noida, U.P., India. Electronic address: shobhitpharmacist@gmail.com.

Fahad Saad Alhodieb (FS)

Department of Clinical Nutrition, College of Applied Health Sciences in Arrass, Qassim University, P.O. BOX:6666, Buraidah, 51452, Saudi Arabia. Electronic address: f.alhodieb@qu.edu.sa.

Md Abul Barkat (MA)

Department of Pharmaceutics, College of Pharmacy, University of Hafr Al-Batin, Al Jamiah, Hafr Al Batin, 39524, Saudi Arabia. Electronic address: abulbarkat05@gmail.com.

Mohd Zaheen Hassan (MZ)

Department of Pharmaceutical Chemistry, College of Pharmacy, King Khalid University, Abha, Saudi Arabia. Electronic address: mzhapharma@gmail.com.

Harshita Abul Barkat (HA)

Department of Pharmaceutics, College of Pharmacy, University of Hafr Al-Batin, Al Jamiah, Hafr Al Batin, 39524, Saudi Arabia. Electronic address: harshiab001@gmail.com.

Raisuddin Ali (R)

Department of Pharmaceutics & Research Center, College of Pharmacy, King Saud University, Saudi Arabia. Electronic address: aliraisuddin786@gmail.com.

Perwaiz Alam (P)

Department of Pharmaceutical Chemistry, School of Pharmaceutical Education & Research, Jamia Hamdard, New Delhi, India. Electronic address: perwaizalam786@gmail.com.

Ozair Alam (O)

Department of Pharmaceutical Chemistry, School of Pharmaceutical Education & Research, Jamia Hamdard, New Delhi, India. Electronic address: dr.ozairalam@gmail.com.

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Classifications MeSH