This is an outdated version published on 28-06-2023. Read the most recent version.
Forthcoming

Effect of heavy metals on germination, biochemical, antioxidant and withanolide content in Withania somnifera (L.) Dunal

Authors

DOI:

https://doi.org/10.14719/pst.2366

Keywords:

Withania somnifera, Withanolide A, Withaferin A, Antioxidant activity, LD50

Abstract

Withania somnifera (L.) Dunal., commonly referred to as Ashwagandha, is a medicinal plant from the solanaceae family with a wide range of pharmacological properties. W. somnifera is a rich source of withanolides, such as withanolide A, withanolide B, withanolide D, withaferin A, etc. and these molecules are attributed for large number of pharmacological activities. In the present study, the impact of heavy metals such as cadmium (Cd), mercury (Hg), and lead (Pb) has been assessed on the growth, biochemical parameters, antioxidant activity and withanolide A and withaferin A content of W. somnifera. The seeds of W. somnifera were germinated in cocopeat treated with different concentrations of Cd (0–200 ppm), Hg (10–100 ppm), and Pb (0–2000 ppm) for 21 days. There have been substantial differences between the heavy metal-treated plants and the control plants with the lowest germination of 20% has been observed in the plants treated with 2000 ppm Pb. The selected metals inhibited vegetative growth with lowest length of 3.07 cm and lowest biomass of 0.74 g in 180 ppm Cd and 200 ppm Cd treated plants respectively. With the addition of heavy metals, biochemical parameters like protein, carbohydrate, chlorophyll, total phenol, flavonoid, and proline content varied significantly and showed metal tolerance by exhibiting antioxidant activity at lower concentrations. The metal accumulation occurred in a dose-dependent manner with highest Cd accumulation of 14.30 mg kg?1, Hg accumulation of 42.45 mg kg?1, and Pb accumulation of 217.46 mg kg?1 of dry biomass of the plants. The withanolide content increased up to a specific metal concentration and decreased with a further increase in heavy metal concentration. The seeds treated with 1200 ppm of Pb showed the highest withanolide A content of 1.7 mg g?1 DW, and the seeds treated with 80 ppm of Cd showed the highest withaferin A content of 3.2 mg g?1 DW.

Downloads

Download data is not yet available.

References

Afewerky HK, Ayodeji AE, Tiamiyu BB, Orege JI, Okeke ES, Oyejobi AO, et al. Critical review of the Withania somnifera (L.) Dunal: ethnobotany, pharmacological efficacy, and commercialization significance in Africa. Bull Natl Salmon Resour Cent. 2021;45(1):176.

Kulkarni SK, Dhir A. Withania somnifera: an Indian ginseng. Prog Neuropsychopharmacol Biol Psychiatry. 2008;32(5):1093–105.

Balkrishna A, Sinha S, Srivastava J, Varshney A. Withania somnifera (L.) Dunal whole-plant extract demonstrates acceptable non-clinical safety in rat 28-day subacute toxicity evaluation under GLP-compliance. Sci Rep. 2022;12(1):11047.

Saggam A, Limgaokar K, Borse S, Chavan-Gautam P, Dixit S, Tillu G, et al. Withania somnifera (L.) Dunal: Opportunity for clinical repurposing in COVID-19 management. Front Pharmacol. 2021;12:623795.

Mukherjee PK, Banerjee S, Biswas S, Das B, Kar A, Katiyar CK. Withania somnifera (L.) Dunal - Modern perspectives of an ancient Rasayana from Ayurveda. J Ethnopharmacol. 2021;264:113157.

Kalra R, Kaushik N. Withania somnifera (Linn.) Dunal: a review of chemical and pharmacological diversity. Phytochem Rev. 2017;16(5):953–87.

Newswire CDN, Sandle T. Ashwagandha market future demand, business strategies, industry growth, regional outlook, challenges and forecast by 2029 [Internet]. Digital Journal. Digital Journal Inc; 2022 [cited 2023 Jan 12]. Available from: https://www.digitaljournal.com/pr/ashwagandha-market-future-demand-business-strategies-industry-growth-regional-outlook-challenges-and-forecast-by-2029

Ahlawat S, Saxena P, Ali A, Khan S, Abdin MZ. Comparative study of withanolide production and the related transcriptional responses of biosynthetic genes in fungi elicited cell suspension culture of Withania somnifera in shake flask and bioreactor. Plant Physiol Biochem. 2017; 114:19–28.

Kalaivanan D, Ganeshamurthy AN. Mechanisms of heavy metal toxicity in plants. In: Rao NKS, Shivashankara KS, Laxman RH, editors. Abiotic stress physiology of horticultural crops. New Delhi: Springer India; 2016. p. 85–102.

Briffa J, Sinagra E, Blundell R. Heavy metal pollution in the environment and their toxicological effects on humans. Heliyon. 2020;6(9):e04691.

Haider FU, Liqun C, Coulter JA, Cheema SA, Wu J, Zhang R, et al. Cadmium toxicity in plants: Impacts and remediation strategies. Ecotoxicol Environ Saf. 2021;211:111887.

Gworek B, Dmuchowski W, Baczewska-D?browska AH. Mercury in the terrestrial environment: a review. Environmental Sciences Europe. 2020;32(1):1–19.

Pourrut B, Shahid M, Dumat C, Winterton P, Pinelli E. Lead uptake, toxicity, and detoxification in plants. Rev Environ Contam Toxicol. 2011;213:113–36.

Mehes-Smith M, Nkongolo K, Cholew E. Coping mechanisms of plants to metal contaminated soil. In: Silvern S and Young S, editors. Environmental Change and Sustainability.London: InTechOpen; 2013. p. 314

Behera B, Bhattacharya S. The importance of assessing heavy metals in medicinal herbs: a quantitative study. Cell Med. 2016;6(1):3.1–3.4.

Asgari Lajayer B, Ghorbanpour M, Nikabadi S. Heavy metals in contaminated environment: Destiny of secondary metabolite biosynthesis, oxidative status and phytoextraction in medicinal plants. Ecotoxicol Environ Saf. 2017;145:377–90.

Nasim SA, Dhir B. Heavy metals alter the potency of medicinal plants. Rev Environ Contam Toxicol. 2010;203:139–49.

Saidulu C, Venkateshwar C, Rao SG. HPLC analysis of withanolides in heavy metal treated plant drug parts (leaves and roots) of Withania somnifera (L) Dunal. World Journal of [Internet]. 2014; Available from: https://www.cabdirect.org/cabdirect/abstract/20143335628

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–75.

DuBois M, Gilles KA, Hamilton JK, Rebers PA, Smith F. Colorimetric method for determination of sugars and related substances. Anal Chem. 1956;28(3):350–6.

Arnon DI. Copper enzymes in isolated chloroplasts. polyphenoloxidase in Beta vulgaris. Plant Physiol. 1949;24(1):1–15.

Bates LS, Waldren RP, Teare ID. Rapid determination of free proline for water-stress studies. Plant Soil. 1973;39(1):205–7.

Sembiring EN, Elya B, Sauriasari R. Phytochemical screening, total flavonoid and total phenolic content and antioxidant activity of different parts of Caesalpinia bonduc (L.) roxb. Pharmacogn J. 2017;10(1):123–7.

Chandana C. Heavy metal accumulation and the biochemical responses in selected medicinal plants. School of Bio Sciences [thesis]. Athirampuzha: Mahatma Gandhi University; 2018.

Blois MS. antioxidant determinations by the use of a stable free radical. Nature. 1958;181(4617):1199–200.

Chew YL, Goh JK, Lim YY. Assessment of in vitro antioxidant capacity and polyphenolic composition of selected medicinal herbs from Leguminosae family in Peninsular Malaysia. Food Chem. 2009 Sep 1;116(1):13–8.

Chung IM, Ali M, Praveen N, Yu BR, Kim SH, Ahmad A. New polyglucopyranosyl and polyarabinopyranosyl of fatty acid derivatives from the fruits of Lycium chinense and its antioxidant activity. Food Chem. 2014;151:435–43.

Uarrota VG, Moresco R, Schmidt EC, Bouzon ZL, Nunes E da C, Neubert E de O, et al. The role of ascorbate peroxidase, guaiacol peroxidase, and polysaccharides in cassava (Manihot esculenta Crantz) roots under postharvest physiological deterioration. Food Chem. 2016;197(Pt A):737–46.

Varshney DS. Effect of some heavy metals on the growth and development of some medicinally important Plants. Botany [thesis]. Aligarh: Aligarh Muslim University; 2014.

Turek A, Wieczorek K, Wolf WM. digestion procedure and determination of heavy metals in sewage sludge—an Analytical problem. Sustain Sci Pract Policy. 2019 Mar 22;11(6):1753.

Praveen N, Murthy HN. Production of withanolide-A from adventitious root cultures of Withania somnifera. Acta Physiol Plant. 2010 Sep 1;32(5):1017–22.

Zhang H, Zhang G, Lü X, Zhou D, Han X. Salt tolerance during seed germination and early seedling stages of 12 halophytes. Plant Soil. 2015;388(1):229–41.

Sethy SK, Ghosh S. Effect of heavy metals on germination of seeds. J Nat Sci Biol Med. 2013;4(2):272–5.

Liu JG, Zhang YX, Shi PL, Chai TY. Effect of cadmium on seed germination and antioxidative enzymes activities in cotyledon of Solanum nigrum L. Sci China Life Sci.2012 Sep;55(9):793-9.

Seneviratne M, Rajakaruna N, Rizwan M, Madawala HMSP, Ok YS, Vithanage M. Heavy metal-induced oxidative stress on seed germination and seedling development: a critical review. Environ Geochem Health.;41(4):1813–31.

Singh S, Parihar P, Singh R, Singh VP, Prasad SM. Heavy metal tolerance in plants: Role of transcriptomics, proteomics, metabolomics, and ionomics. Front Plant Sci. 2015;6:1143.

Parmar, Dave, Sudhir, Panchal. Physiological, biochemical and molecular response of plants against heavy metals stress. Afr J Curr Med Res. 2013;5(1):80–9.

Prasad TK. Mechanisms of chilling-induced oxidative stress injury and tolerance in developing maize seedlings: changes in antioxidant system, oxidation of proteins and lipids, and protease activities. Plant J. 1996;10(6):1017–26.

Choudhary M, Jetley UK, Abash Khan M, Zutshi S, Fatma T. Effect of heavy metal stress on proline, malondialdehyde, and superoxide dismutase activity in the cyanobacterium Spirulina platensis-S5. Ecotoxicol Environ Saf. 2007 Feb;66(2):204–9.

Palma JM, Sandalio LM, Javier Corpas F, Romero-Puertas MC, McCarthy I, del Río LA. Plant proteases, protein degradation, and oxidative stress: role of peroxisomes. Plant Physiol Biochem. 2002;40(6):521–30.

Lin YC, Kao CH. Proline accumulation induced by excess nickel in detached rice leaves. Biol Plant. 2007;51(2):351–4.

Küpper, Küpper, Spiller. Environmental relevance of heavy metal-substituted chlorophylls using the example of water plants. J Exp Bot. 1996;47(2):259–66.

Trivedi LD. A study on interactive effects of heavy metal on growth and biochemical changes in medicinal plants. Botany [thesis]. Ahmedabad: Gujarat University; 2005.

Michalak A. Phenolic compounds and their antioxidant activity in plants growing under heavy metal stress. Pol J Environ Stud [Internet]. 2006;15(4):523-530

Parry AD, Tiller SA, Edwards R. The Effects of Heavy Metals and Root Immersion on Isoflavonoid Metabolism in Alfalfa (Medicago sativa L.). Plant Physiol. 1994 Sep;106(1):195–202.

Dursun K, Kayir O, Sa?lam N, ?ahin S. Lokman O, Mahfuz E. Changes of phenolic compounds in tomato associated with the heavy metal stress. J Nat Agents Mol Ther. 2019; 2 (1):35–43.

Nadgórska-Socha A, Kafel A, Kandziora-Ciupa M, Gospodarek J, Zawisza-Raszka A. Accumulation of heavy metals and antioxidant responses in Vicia faba plants grown on monometallic contaminated soil. Environ Sci Pollut Res Int. 2013;20(2):1124–34.

Schreck E, Foucault Y, Sarret G, Sobanska S, Cécillon L, Castrec-Rouelle M, et al. Metal and metalloid foliar uptake by various plant species exposed to atmospheric industrial fallout: mechanisms involved for lead. Sci Total Environ. 2012;427-428:253–62.

Antony A, Nagella P. Effect of heavy metals on the andrographolide content, phytochemicals and antioxidant activity of Andrographis paniculata. Asian J Chem. 2020;32(11):2748–52.

Li X, Wang S, Guo L, Huang L. Effect of cadmium in the soil on growth, secondary metabolites and metal uptake in Salvia miltiorrhiza. Toxicol Environ Chem. 2013;95(9):1525–38.

Published

28-06-2023

Versions

How to Cite

1.
Banadka A, Nagella P. Effect of heavy metals on germination, biochemical, antioxidant and withanolide content in Withania somnifera (L.) Dunal. Plant Sci. Today [Internet]. 2023 Jun. 28 [cited 2024 Dec. 22];. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/2366

Issue

Section

Research Articles

Similar Articles

You may also start an advanced similarity search for this article.