اخبار و اعلانات

 آمار

تعداد نشریات282
تعداد نشریات سازمان80
تعداد شماره‌ها3,208
تعداد مقالات35,560
تعداد مشاهده مقاله53,001,568
تعداد دریافت فایل اصل مقاله92,287,538
Labbafi, Mohammad Reza, Qavami, Nassrin, Zarinpanjeh, Nassim. (1403). The Impact of Elicitor (Chemical and Physical) and Explant Source on the Synthesis of Silymarin Through Suspension Culture of Silybum marianum: A Meta-Analysis. سامانه مدیریت نشریات علمی, 13(4), 1055-1061. doi: 10.22034/jmpb.2023.363988.1624
Mohammad Reza Labbafi; Nassrin Qavami; Nassim Zarinpanjeh. "The Impact of Elicitor (Chemical and Physical) and Explant Source on the Synthesis of Silymarin Through Suspension Culture of Silybum marianum: A Meta-Analysis". سامانه مدیریت نشریات علمی, 13, 4, 1403, 1055-1061. doi: 10.22034/jmpb.2023.363988.1624
Labbafi, Mohammad Reza, Qavami, Nassrin, Zarinpanjeh, Nassim. (1403). 'The Impact of Elicitor (Chemical and Physical) and Explant Source on the Synthesis of Silymarin Through Suspension Culture of Silybum marianum: A Meta-Analysis', سامانه مدیریت نشریات علمی, 13(4), pp. 1055-1061. doi: 10.22034/jmpb.2023.363988.1624
Labbafi, Mohammad Reza, Qavami, Nassrin, Zarinpanjeh, Nassim. The Impact of Elicitor (Chemical and Physical) and Explant Source on the Synthesis of Silymarin Through Suspension Culture of Silybum marianum: A Meta-Analysis. سامانه مدیریت نشریات علمی, 1403; 13(4): 1055-1061. doi: 10.22034/jmpb.2023.363988.1624

The Impact of Elicitor (Chemical and Physical) and Explant Source on the Synthesis of Silymarin Through Suspension Culture of Silybum marianum: A Meta-Analysis

Journal of Medicinal plants and By-products
مقاله 15، دوره 13، شماره 4، اسفند 2024، صفحه 1055-1061    اصل مقاله (826.41 K)
نوع مقاله: Research Paper
شناسه دیجیتال (DOI): 10.22034/jmpb.2023.363988.1624
نویسندگان
Mohammad Reza Labbafi؛ Nassrin Qavami؛ Nassim Zarinpanjeh*
Medicinal Plants Research Center, Institute of Medicinal Plants, ACECR, Karaj, Iran
چکیده
Silybum marianum (L.) Gaertn., commonly known as milk thistle, is renowned for its bioactive compounds, particularly silymarin, which holds significant potential for its neuro-protective, antioxidant, anticancer, antidiabetic, antiviral, antihypertensive, anti-inflammatory, photoprotective, and hepatoprotective properties. The investigation of these factors and their interplay within the context of silymarin biosynthesis is anticipated to provide valuable insights into optimizing production processes for pharmaceutical and nutraceutical applications. In the present context, a compilation of data has been undertaken, followed by a meta-analysis, aimed at investigating the influence of elicitor (chemical and physical) and explant source (cotyledon, hypocotyl, and leaf) on silymarin production within the suspension cultures of S. marianum. Data was gathered on treatment means and sample sizes (n) concerning the production of silymarin under both control and elicited conditions. The effect size was computed using the natural logarithm of the response ratio (lnRR) as a metric to gauge the influence of elicitor treatments on silymarin production when compared to the control.
کلیدواژه‌ها
Cell culture؛ Meta-analysis؛ Milk thistle؛ Secondary metabolites
مراجع
  1. Li F., Yang L., Zhao T., Zhao J., Zou Y., Zou Y., Wu X. Optimization of enzymatic pre-treatment for n-hexaneextraction of oil from Silybum marianum seeds using response surface methodology. Food and Bioprod Process. 2012; 90: 87-94.
  2. Wadhwa K., Pahwa R., Kumar M., Kumar S., Sharma P.C., Singh G., Verma R., Mittal V., Singh I., Kaushik D., Jeandet P. Mechanistic Insights into the Pharmacological Significance of Silymarin. Molecules. 2022; 27:5327.
  3. Fraschini F., Demartini G., Esposti D. Pharmacology of Silymarin. Clin Drug Invest. 2002; 22: 51-65.
  4. Gillessen A., Schmidt H.H.J. Silymarin as Supportive Treatment in Liver Diseases: A Narrative Review. Adv Ther. 2020; 37:1279-1301.
  5. Singh M., Kadhim M.M., Turki Jalil A., Oudah S.K., Aminov Z., Alsaikhan F., Jawha Z.H., Ramirez‑Coronel A.A., Farhood B. A systematic review of the protective effects of silymarin/silibinin against doxorubicin‑induced cardiotoxicity. Cancer Cell Int. 2023; 23:1-16.
  6. Elateeq A.A., Sun Y., Nxumalo W., Gabr A.M.M. Biotechnological production of silymarin in Silybum marianum L.: A review. Biocatal Agric Biotechnol. 2020:29.
  7. Nikalje G.C., Zimare S.B., Shelke D.B. Effect of elicitors on plant cell suspension culture for the enhancement of secondary metabolite production. Nat J. Pharm Sci. 2021; 1:50-57.
  8. Singh A., Dwivedi P. Methyl-jasmonate and salicylic acid as potent elicitors for secondary metabolite production in medicinal plants: A review. J Pharmacogn Phytochem. 2018; 7:750-757.
  9. Chandran H., Meena M., Barupal T., Sharma K. Plant tissue culture as a perpetual source for production of industrially important bioactive compounds. Biotechnol Rep. 2020; 26:e00450.
  10. Radman R., Saez T., Bucke C., Keshavarz T. Elicitation of plants and microbial cell systems. Biotechnol Appl Biochem. 2003; 37:91-102.
  11. Wang J.W., Wu J.Y. Effective elicitors and process strategies for enhancement of secondary metabolite production in hairy root cultures, in: Doran, P.M. (Ed.), Biotechnology of Hairy Root Systems. Advances in Biochemical Engineering/Biotechnology, Springer, Berlin, Heidelberg. 2013, pp. 55-89.
  12. Halder M., Sarkar S., Jha S. Elicitation: A biotechnological tool for enhanced production of secondary metabolites in hairy root cultures. Eng Life Sci. 2019; 880-895.
  13. Asghari F., Hossieni B., Hassani A., Shirzad H. Effect of explants source and different hormonal combinations on direct regeneration of basil plants (Ocimum basilicum L.). Aust J. Agri Engin. 2012; 3:12-17.
  14. Lau J., Rothstein H.R., Stewart G.B. History and progress of meta-analysis. Handbook of Meta-Analysis in Ecology and Evolution (eds J. Koricheva,J. Gurevitch & K. Mengersen), Princeton University Press, Princeton and Oxford. 2013, pp. 407-419.
  15. Koricheva J., Gurevitch J. Uses and misuses of meta-analysis in plant ecology. J. Ecol. 2014; 102:828-844.
  16. Davoodi A., Khoshvishkaie E., Azadbakht M. Plant cells technology as an effective biotechnological approach for high scale production of pharmaceutical natural compounds; A meta-analysis study. Pharm Biomed. Res. 2019; 5:1-9.
  17. Zhang X., Shabala S., Koutoulis A., Shabala L., Zhou M. Meta-analysis of major QTL for abiotic stress tolerance in barley and implications for barley breeding. Planta. 2017; 245:283-295.
  18. Draga S., Gabelli G., Palumbo F., Barcaccia G. Genome-Wide Datasets of Chicories (Cichorium intybus L.) for Marker-Assisted Crop Breeding Applications: A Systematic Review and Meta-Analysis. Int J. Mol Sci. 2023; 24:11663.
  19. Pellegrino E., Bedini S., Nuti M., Ercoli L. Impact of genetically engineered maize on agronomic, environmental and toxicological traits: a meta-analysis of 21 years of field data. Sci Rep. 2018; 8:3113.
  20. Li M., Xu J., Gao Z., Tian H., Gao Y., Kariman K. Genetically modified crops are superior in their nitrogen use efficiency-A meta-analysis of three major cereals. Sci Rep. 2020; 10:8568.
  21. Windley H.R., Starrs D., Stalenberg E., Rothman J.M., Ganzhorn J.U., Foley, W.J. Plant secondary metabolites and primate food choices: A meta‐analysis and future directions. Am J. Primatol. 2020; 84:e23397.
  22. Gaynor M.L., Lim-Hing S., Mason C.M. Impact of genome duplication on secondary metabolite composition in non-cultivated species: a systematic meta-analysis. Ann Bot. 2020; 126:363-376.
  23. Augé R.M., Toler H.D., Saxton A.M. Mycorrhizal stimulation of leaf gas exchange in relation to root colonization, shoot size, leaf phosphorus and nitrogen: A quantitative analysis of the literature using meta-regression. Front Plant Sci. 2016; 7:1084.
  24. Rezapour A., Labbafi M.R., Oja T. The impact of soil warming on fine root trait responses of trees, deciduous vs. coniferous: a meta-analysis. Forestry Studies. 2023; 77:67-75
  25. Higgins J.P., Thompson S.G. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002; 21:1539-58.
  26. Cai Z., Kastell A., Knorr D., Smetanska I. Exudation: an expanding technique for continuous production and release of secondary metabolites from plant cell suspension and hairy root cultures. Plant Cell Rep. 2012; 31:461-477.
  27. Patel H., Krishnamurthy R. Elicitors in plant tissue culture. J. Pharmacogn Phytochem. 2013; 2:60-65.
  28. Gaume A., Komarnytsky S., Borisjuk N., Raskin I. Rhizosecretion of recombinant proteins from plant hairy roots. Plant Cell Rep. 2003; 21:1188-1193.
  29. Karadi R.V., Kavatagimath S.A., Gaviraj E.N., Sastry D.N., Chandrashekhara S., Rajarajeshwari N. Evaluation of Plumbago indica callus for its plumbagin content and antimicrobial activity. J. Cell Tiss Res. 2007; 7:1131-1136.
  30. Tumova L., Gallova K., Rimakova J., Dolezal M., Tuma J. The effect of substituted amides of pyrazine-2-carboxylic acids on flavonolignan production in Silybum marianum culture in vitro. Acta Physiol Plant. 2005; 27:257-262.
  31. Sánchez-Sampedro M.A., Fernandez-Tarrago J., Corchete P. Elicitation of silymarin in cell cultures of Silybum marianum: effect of subculture and repeated addition of methyl jasmonate. Biotechol Lett. 2009; 3:1633-1637.
  32. Madrid E., Corchete P. Silymarin secretion and its elicitation by methyl jasmonate in cell cultures of Silybum marianum is mediated by phospholipase Dphosphatidic acid. J. Exp Bot. 2010; 61:747-754.
  33. Tumova L., Tuma J., Dolezal M. Pyrazinecarboxamides as potential elicitors of flavonolignan and flavonoid production in Silybum marianum and Ononis arvensis cultures in vitro. Molecules. 2011; 16:9142-9152.
  34. El Sherif F., Khattab S., Ibrahim A.K., Ahmed S.A. Improved silymarin content in elicited multiple shoot cultures of Silybum marianum L. Physiol Mol Biol Plants. 2013; 19:127-136.
  35. Firouzi A., Mohammadi S.A., Khosrowchahli M., Movafeghi A., Hasanloo T. Enhancement of silymarin production in cell culture of Silybum marianum (L) Gaertn by elicitation and precursor feeding. J. Herbs Spices Med Plants. 2013; 19:262-274.
  36. Roustakhiz J., Saboki E. Plant tissue culture of Silybum marianum L. and check out elicitor effect on the amount of silymarin. J. Nov Appl Sci. 2016; 5:161-168.
  37. Elsharnouby M.E., Hassan F.A.S. Improvement of silymarin content in cell cultures of Silybum marianum by copper sulphate elicitor. Acta Sci Pol Hortorum Cultus. 2018; 17:105-114.
  38. Ho T.T., Murthy H.N., Park S.Y. Methyl Jasmonate Induced Oxidative Stress and Accumulation of Secondary Metabolites in Plant Cell and Organ Cultures. Int J. Mol Sci. 2020; 21:716.
  39. Sanchez-Sampedro M.A., Fernandez-Tarrago J., Corchete P. Yeast extract and methyl jasmonate-induced silymarin production in cell cultures of Silybum marianum (L.) Gaertn. J. Biotechnol. 2005; 119:60-69.
  40. Gabr A.M.M., Ghareeb H., El Shabrawi H.M., Smetanska I., Bekheet S.A. Enhancement of silymarin and phenolic compound accumulation in tissue culture of Milk thistle using elicitor feeding and hairy root cultures. J. Genet Engin Biotech. 2016; 14:327-333.
  41. Elwekeel A., AbouZid S., Sokkar N., Elfishway A. Studies on flavanolignans from cultured cells of Silybum marianum. Acta Physiol Plant. 2012; 34:1445-1449
  42. Pourjabar A., Azimi M.R., Mostafaie A., Kahrizi D., Cheghamirza K. Proteome analysis of Milk thistle (Silybum marianum L.) cell suspension cultures in response to methyl jasmonate and yeast extract elicitors. Appl. Ecol. Environ Res. 2018; 17:547-560.
  43. Shah J., Klessig D.F. Salicylic acid: signal perception and transduction. In: Libbenga K, Hall M, Hooykaas PJJ (eds) Biochemistry and molecular biology of plant hormones. Elsevier, Oxford. 1999; 513-541.
  44. Hirano S., Nagao N. Effects of chitosan, pectic acid, lysozyme, and chitinase on the growth of several phytopathogens. Agric. Biological Chem. 1989; 53:3065-3066.
  45. Cuero R.G., Duffus E., Osuji G., Pettit R. Aflatoxin control in preharvest maize: Effects of chitosan and two microbial agents. J. Agric Sci. 1991; 117:165-169.
  46. Benhamou N., Lafontaine P.J., Nicole M. Induction of systemic resistance to Fusarium crown and root rot in tomato plants by seed treatment with chitosan. Phytopathology. 1994; 84:1432-1444.
  47. Shah M., Jan H., Drouet S., Tungmunnithum D., Shirazi J.H., Hano C., Abbasi BH. Antioxidant and Anti-Inflammatory Activities of Cell Extracts. Molecules. 2021; 26:791.
  48. Zhao J., Davis L.C., Verpoorte R. Elicitor signal transduction leading to production of plant secondary metabolites. Biotechnol Adv. 2005; 23:283-333.
  49. Khalili M., Hasanloo T., Kazemi Tabar S.K. Ag+ enhanced silymarin production in hairy root cultures of Silybum marianum (L.) Gaertn. Plant Omics. 2010; 3:109-114.
  50. Vildová A., Hendrychová H., Kubeš J., Tůmová L. Influence of AgNO3 treatment on the flavonolignan production in cell suspension culture of Silybum marianum (L.) Gaertn. Int Schol Sci Res Innov. 2014; 8:959-962.
  51. Twaij B.M., Hasan M.N. Bioactive Secondary Metabolites from Plant Sources: Types, Synthesis, and Their Therapeutic Uses. Int J. Plant Biol. 2022; 13:4-14.
  52. Taghizadeha M., Nasibia F., Manouchehri Kalantaria K., Benakashanib F. Callogenesis optimization and cell suspension culture establishment of Dracocephalum polychaetum Bornm. and Dracocephalum kotschyi Boiss.: An in vitro approach for secondary metabolite production. S Afr J. Bot. 2020; 132:79-86.
  53. Kriaa D., Naceur M.B., Mereu A.R., Scarpa G.M. Secondary metabolites production from cell suspension culture of Citrus aurantium L. Plant Cell Biotechnol Mol Biol. 2019; 20:140-151.
  54. Mamdouh D., Smetanska I. Optimization of callus and cell suspension cultures of Lycium schweinfurthii for improved production of phenolics, flavonoids, and antioxidant activity. Horticulturae. 2022; 8:394.
  55. Ahmadpoor F., Zare N., Asghari R., Sheikhzadeh-Mosadeg P. The effect of plant growth regulators on the antioxidant enzyme activity and secondary metabolite production in the cell suspension cultures of Melia azedarach L. The J. Horticulture Sci. Biotechnology. 2023; 98:662-677.
  56. Shehzad M.A., Khan M.A., Ali A., Mohammad S., Noureldeen A., Darwish H., Ali A., Ahmad A., Khan T., Khan R.S. Interactive effects of zinc oxide nano particles and different light regimes on growth and silymarin biosynthesis in callus cultures of Silybum marianum L., Artificial Cells, Nanomed Biotech. 2021; 49:523-535.
  57. Eari S., Aghdasi M., Ahmadzadeh E., Mianabadi M. Influence of Plant Growth Regulators on Callus Induction, Silymarin Production and Antioxidant Activity in Milk Thistle (Silybum marianum L. Gaertn.) under Tissue Culture Medium. J. Med Plants and By-products. 2017; 1:59-69.
آمار
تعداد مشاهده مقاله: 531
تعداد دریافت فایل اصل مقاله: 539


counter
سامانه مدیریت نشریات علمی. طراحی و پیاده سازی از سیناوب