Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Aug 28;9(10):5755-5764.
doi: 10.1002/fsn3.2544. eCollection 2021 Oct.

Onosma mutabilis: Phytochemical composition, antioxidant, cytotoxicity, and acute oral toxicity

Affiliations

Onosma mutabilis: Phytochemical composition, antioxidant, cytotoxicity, and acute oral toxicity

Ahmed Aj Jabbar. Food Sci Nutr. .

Abstract

The traditional use of Onosma L. species as a remedy motivated scientists to discover great biological/pharmacological potentials in this plant. In the current study, in addition to the phytochemical composition of methanol (MeOH), water, and ethyl acetate extract of aerial parts of Onosma mutabilis Boiss., an endemic plant species in the flora of Kurdistan, Iraq, in vitro antioxidant, cytotoxicity, and oral toxicity activity were investigated. Results of total phenolic and total flavonoid tests show the MeOH extract superiority, and the results of Gas chromatography-mass spectrophotometer(GS/GS-MS) show 18 chemical compounds in the MeOH extract, and the majority of the detected compounds were alkaloids (78.77%) and steroids (11.48%), namely as 5,8-dihydroxy-2-(4-methylpent-3-enyl) naphthalene-1,4-dione (48.60%), 3-O-Methyl-d-glucose (27.49%), β-Sitosterol (6.81%), Phenol, 2,4-bis (1,1-dimethyl ethyl)-, phosphite (3.46%), and 24,25-Dihydroxycholecalciferol (3.14%). Results of the antioxidant tests show the MeOH extract superiority in the phosphomolybdenum assay, radical scavenging [on 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS)] assays, and reducing power [cupric reducing antioxidant capacity (CUPRAC) and ferric reducing antioxidant power (FRAP)] assays (1.45, 3.54, 2.33, 1.12, 1.62, mg/ml, respectively). The cytotoxicity results of the plant extract are presented as IC50 (inhibitory concentration at 50%) on the prostate cancer cells (DU-145), mammary cancer cells (MCF-7), and human cervix carcinoma (Hep2c), at which values ranged from 28.79 to 41.83 μg/ml. Results of the acute toxicity in the dose-dependent trail (100, 200, 300, 600 mg/kg of MeOH) show the absence of the behavior and appearance changes of female Wister rats. Overall, O. mutabilis extract exhibited significant natural potentials probably because of its polar phytochemicals, which could be an alternative source for remedial, nutrient, and cosmetic manufacture.

Keywords: Onosma mutabilis; antioxidant; cytotoxicity; oral toxicity; phytochemistry.

PubMed Disclaimer

Conflict of interest statement

The author declares no conflict of interest.

Figures

FIGURE 1
FIGURE 1
The general appearance of Onosma Mutabilis in the nature
FIGURE 2
FIGURE 2
Chromatogram of methanolic extract Of O. Mutabilis. 1‐18 represent chromatogram of 2‐(5‐Acetyl‐2‐Furyl)‐1,4‐Naphthoquinone, Dodecane, 3‐Methyl‐, Pentacosane, Cyclopentane, 1,2‐Dimethyl‐3‐(1‐Methylethenyl)‐, 2‐Octyne, 5,8‐dihydroxy‐2‐4‐methylpent‐3‐enyl,naphthalene‐1,4‐dione (Deoxy shikonon), Octadecane, N‐Dodecyl Glycidyl Ether, Diisooctyl Phthalate, 3‐O‐Methyl‐D‐Glucose, 1‐Nonadecene, Eicosane, 2,4,6‐Trimethylmorpholine, 24,25‐Dihydroxycholecalciferol, Delta.5‐Ergostenol, Β‐Sitosterol, 1‐Heptatriacotanol, Phenol, 2,4‐bis(1,1‐dimethylethyl)‐, phosphite

Similar articles

Cited by

References

    1. Ahmad, V. U. , Kousar, F. , Khan, A. , Zubair, M. , Iqbal, S. , & Tareen, R. B. (2005). A new ketone and a known anticancer triterpenoid from the leaves of Onosma limitaneum . Helvetica Chimica Acta, 88(2), 309–311. 10.1002/hlca.200590013 - DOI
    1. Attar, F. , & Joharchi, M. R. (2006). Onosma khorassanica, a new species from northeast of Iran. Rostaniha, 7(Supplement. 2), 111–114.
    1. Aung, T. N. , Qu, Z. , Kortschak, R. D. , & Adelson, D. L. (2017). Understanding the effectiveness of natural compound mixtures in cancer through their molecular mode of action. International Journal of Molecular Sciences, 18(3), 656. 10.3390/ijms18030656 - DOI - PMC - PubMed
    1. Autian, J. (1973). Toxicity and health threats of phthalate esters: Review of the literature. Environmental Health Perspectives, 4, 3–26. 10.1289/ehp.73043 - DOI - PMC - PubMed
    1. Awad, A. B. , Fink, C. S. , Williams, H. , & Kim, U. (2001). In vitro and in vivo (SCID mice) effects of phytosterols on the growth and dissemination of human prostate cancer PC‐3 cells. European Journal of Cancer Prevention, 10(6), 507–513. 10.1097/00008469-200112000-00005 - DOI - PubMed

LinkOut - more resources