Cited by 11Wound Healing and TreatmentsPhytochemistry and Biological ActivitiesPhytochemistry and biological activity of medicinal plants

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Antibacterial and Anti-inflammatory Activity of Extracts and Major Constituents Derived from Stachytarpheta indica Linn. Leaves and Their Potential Implications for Wound Healing

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Agampodi, Vajira Asela, Katavic, Peter, Collet, Christopher, Collet, Trudi·2022·Applied Biochemistry and Biotechnology

Abstract

Wounds of various types continue to have a severe socioeconomic impact on the cost of health care. Globally, there has been increased interest surrounding the identification of bioactive compounds that promote or modulate the wound healing process. Stachytarpheta indica Linn. is traditionally used to heal wounds and relieve inflammation; however, the theorised pharmacological properties have not yet been scientifically validated. In this study, dried and ground plant leaves were extracted with water and methanol, which were then subjected to various analyses. The antimicrobial activity of the plant extracts and isolated compounds was determined using well diffusion assays, while the minimum inhibitory concentrations were determined with a colorimetric assay. Morphological changes of human keratinocytes in response to plant extracts were observed with differential interference contrast microscope imaging. Cell viability, proliferation, and migratory effects post-treatment with the plant extracts were also evaluated via colorimetric cytotoxicity assays and a real-time cell analyser protocol. Anti-inflammatory effects of plant extracts and isolated compounds were evaluated by flow cytometry and cyclooxygenase and lipoxygenase enzyme inhibition assays. Three active compounds, i.e. ipolamiide, verbascoside and iso-verbascoside, were isolated from S. indica leaves. Verbascoside demonstrated broad-range antibacterial activity and imposed strong inhibition at 9.77 μg/mL against Staphylococci spp. S. indica extracts (0.1-0.2 mg/mL) were shown to improve human keratinocyte proliferation up to 60% and induce morphological changes by producing cytoplasmic projections at concentrations higher than 0.4 mg/mL. Plant extracts (6.25-100 μg/mL) and individual compounds (3.125-50 μg/mL) elicited strong anti-inflammatory effects by suppressing the expression of interleukin-8 and inhibiting cyclooxygenase-1 and 5-lipoxygenase enzymes. Collectively, these results indicate that plant extracts and isolated compounds derived from S. indica have the potential to inhibit bacterial growth, promote tissue regeneration and reduce inflammation, hence, potentially providing the basis for a novel therapeutic for the treatment of wounds.

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Research works printed but not linked: 80

  1. Maver, T., Maver, U., Kleinschek, K. S., Smrke, D. M., & Kreft, S. (2015). A review of herbal medicines in wound healing. International Journal of Dermatology, 54, 740–751. · DOI
  2. Öztürk, F., Ermertcan, A. T., & İnanır, I. (2013). Hyperbaric oxygen therapy for the management of chronic wounds. Cutaneous and Ocular Toxicology, 32(1), 72–77. · DOI
  3. Sen, C. K., Gordillo, G. M., Roy, S., Kirsner, R., Lambert, L., Hunt, T. K., Gottrup, F., Gurtner, G. C., & Longaker, M. T. (2009). Human skin wounds: A major and snowballing threat to public health and the economy. Wound Repair and Regeneration, 17(6), 763–771. · DOI · Paper page
  4. Wiegand, C., Schönfelder, U., Abel, M., Ruth, P., Kaatz, M., & Hipler, U.-C. (2010). Protease and pro-inXammatory cytokine concentrations are elevated in chronic compared to acute wounds and can be modulated by collagen type I in vitro. Archives of Dermatological Research, 302, 419–428. · DOI
  5. Choi, J., Park, Y.-G., Yun, M.-S., & Seol, J.-W. (2018). Effect of herbal mixture composed of Alchemilla vulgaris and Mimosa on wound healing process. Biomedicine and Pharmacotherapy, 106, 326–332. · DOI
  6. Leach, M. J. (2004). Making sense of the venous leg ulcer debate: A literature review. Journal of Wound Care, 13, 52–56. · DOI
  7. Mustoe, T. (2004). Understanding chronic wounds: A unifying hypothesis on their pathogenesis and implications for therapy. The American Journal of Surgery, 187, 65S-70S. · DOI
  8. Percival, S. L., Hill, K. E., Williams, D. W., Hooper, S. J., Thomas, D. W., & Costerton, J. W. (2012). A review of the scientific evidence for biofilms in wounds. Wound Repair and Regeneration, 20, 647–657. · DOI
  9. Palombo, E. A., & Semple, S. J. (2001). Antibacterial activity of traditional Australian medicinal plants. Journal of Ethnopharmacology, 77, 151–157. · DOI
  10. Sibanda, T., & Okoh, A. I. (2007). The challenges of overcoming antibiotic resistance: Plant extracts as potential sources of antimicrobial and resistance modifying agents. African Journal of Biotechnology, 6(25), 2886–2896.
  11. Mariod, A. A., Abdelwahab, S. I., Elkheir, S., Ahmed, Y. M., Fauzi, P. N. M., & Chuen, C. S. (2012). Antioxident activity of different parts from Annona squamosa and Catuaregam nilotica methanolic extract. Acta Scientiarum Polonorum, 11(3), 249–257.
  12. Samy, R. P., Gopalakrishnakone, P., Houghton, P., & Ignacimuthu, S. (2006). Purification of antibacterial agents from Tragia involucrata–a popular tribal medicine for wound healing. Journal of Ethnopharmacology, 107, 99–106. · DOI
  13. Buru, A. S., Pichika, M. R., Neela, V., & Mohandas, K. (2014). In vitro antibacterial effects of Cinnamomum extracts on common bacteria found in wound infections with emphasis on methicillin-resistant Staphylococcus aureus. Journal of Ethnopharmacology, 153, 587–595. · DOI
  14. Somashekar, S. B. (2013). Wound healing and indigenous drugs: Role as antioxidants: A review. Journal of Medical and Health Sciences, 2(2), 5–16.
  15. Ghosh, P. K., & Gaba, A. (2013). Phyto-extracts in wound healing. Journal of Pharmacy and Pharmaceutical Science, 16(5), 760–820. · DOI
  16. Biswas, D., Yoganandam, G., Dey, A., & Deb, L. (2013). Evaluation of antimicrobial and wound healing potentials of ethanol extract of wedelia biflora Linn D. C. leaves. Indian Journal of Pharmaceutical Sciences, 75(2), 156–161.
  17. Baker, S. R., Stacey, M. C., Jopp-McKay, A. G., Hoskin, S. E., & Thompson, P. J. (1991). Epidemiology of chronic venous ulcers. British Journal of Surgery, 78, 864–867. · DOI
  18. Krishna Kumar, H. N., Bhavyashree, K. G., & Chauhan, J. B. (2012). Phytochemical screening and antibacterial activity of Stachytarpheta indica. Global Journal of Pharmacology, 6(1), 4–7.
  19. Chandler, G. T., Westaway, J. O., & Conn, B. J. (2014). Taxanomic uncertainty of Stachytarpheta (Verbenaceae) in the Asia-Pacific and implications for invasive weed recognition and management. Journal of Plant Systematics, 16, 83–88.
  20. Rozianoor, M. H. W., Nadia, K. N., & Nurdiana, S. (2014). Stachytarpheta jamaicensis ethanolic leaf extract as wound healer on alloxan-induced diabetic Sprague Dawley rats. Bio technology An Indian Jouirnal, 9(11), 460–466.
  21. Joshi, V. G., Sutar, P. S., Kargar, A. A., Patil, S. A., Gopalakrishna, B., & Sureban, R. R. (2010). Screening of ethanolic extract of Stachytarpheta indica L. (Vahl) leaves for hepatoprotective activity. International Journal of Research in Ayurveda and Pharmacy, 1(1), 174–179.
  22. Sunday, O. O., Uguru, O. M., & Akanbi, B. E. (2008). Anti-diarrhea effect of aqueous extracts of Momordica balsmina and Stachytarpheta indica in rats. Journal of Natural Products, 1, 36–45.
  23. Ezeabara, C. A., Orachu, L. A., & CU, O., Ilodibia, C. V., Emeka, A. N. & KU, E. . (2015). Comparative study of phytochemical, proximate and mineral compositions of Stachytarpheta cayannensis (L.C. Rich) Schau and Stachytarpheta indica (Linn.) Vahl. International Journal of Plant Biology and Research, 3(1), 1027.
  24. Princely, S., Basha, N. S., Kirubakaran, J. J., & Dhanaraju, M. D. (2013). Preliminary phytochemical screening and antimicrobial activity of aerial parts of Stachytarpheta indica L. (Vahl.). Medicinal Plants, 5(2), 96–101.
  25. Hong, C.-E., & Lyu, S.-Y. (2011). Anti-inflammatory and anti-oxidative effects of Korean red ginseng extract in human keratinocytes. Immune Network, 11(1), 42–49. · DOI
  26. Gierse, J. K., & Koboldt, C. M. (2001). Cyclooxygenase assays. Current protocols in pharmacology, 3(1), 1–16.
  27. Baylac, S., & Racine, P. (2003). Inhibition of 5-lipoxygenase by essential oils and other natural fragrant extracts. International Journal of Aromatherapy, 13(2), 138–142. · DOI
  28. Kamatou, G. P. P., Viljoen, A. M., & Steenkamp, P. (2010). Antioxidant, anti-inflammatory activities and HPLC analysis of South African Salvia species. Food Chemistry, 119(2), 684–688. · DOI
  29. Damtoft, S., Jensen, S. R., & Nielsen, B. J. (1984). The identity of the iridoid glucoside tarphetalin with ipolamiide. Phyrochemistry, 23(4), 907–908. · DOI
  30. Javzan, S., & Selenge, D. (2013). Phytochemical study of aerial parts from Phlomis tuberosa L. Mongolian Journal of Chemistry, 14(40), 2–3.
  31. Kırmızıbekmez, H., Piacente, S., Pizza, C., Donmez, A. A., & Calis, I. (2004). Iridoid and Phenylethanoid Glycosides from Phlomis nissolii and P. capitata. Zeitschrift für Naturforschung B, 59(5), 609–613. · DOI
  32. Yal-Aın, F. N., Erscz, T., Avcıc, K., Gotfredsen, C. H., Jensen, S. R., & Calıs, I. (2007). New iridoid glycosides from Lamium eriocephalum subsp. eriocephalum. Helvetica Chimica Acta, 90, 332–336. · DOI
  33. Akdemir, Z. S., Tatli, I. I., Bedir, E., & Khan, I. A. (2004). Iridoid and phenylethanoid glycosides from Verbascum lasianthum. Turkish Journal of Chemistry, 28, 227–234.
  34. Krebs, H. C., & Habermehl, G. G. (1992). Two-dimensional NMR spectroscopy of G1 ycosides. Magnetic Resonance in Chemistry, 30, S56–S59. · DOI
  35. Phakeovilay, C., Disadee, W., Sahakitpichan, P., Sitthimonchai, S., Kittakoop, P., Ruchirawat, S., & Kanchanapoom, T. (2013). Phenylethanoid and flavone glycosides from Ruellia tuberosa L. Journal of Natural Medicines, 67, 228–233. · DOI
  36. Gomez-Aguirre, Y. A., Zamilpa, A., Gonzalez-Cortazar, M., & Trejo-Tapia, G. (2012). Adventitious root cultures of Castilleja tenuiflora Benth. as a source of phenylethanoid glycosides. Industrial Crops and Products, 36, 188–195. · DOI
  37. Guvenalp, Z., Ozbek, H., Unsalar, T., Kazaz, C., & Demirezer, L. O. (2006). Iridoid, flavonoid, and phenylethanoid glycosides from Wiedemannia orientalis. Turkish Journal of Chemistry, 30, 391–400.
  38. Sobeh, M., Mamadalieva, N. Z., Mohamed, T., Krstin, S., Youssef, F. S., Ashour, M. L., Azimova, S. S., & Wink, M. (2016). Chemical profiling of Phlomis thapsoides (Lamiaceae) and in vitro testing of its biological activities. Medicinal Chemistry Research, 25, 2304–2315. · DOI
  39. Dinda, B., Debnath, S., & Harigaya, Y. (2007). Naturally occurring iridoids. A Review, Part 1. Chemical and Pharmaceutical Bulletin Pharmaceutical Society of Japan, 55(2), 159–222. · DOI
  40. Maquiaveli, C. D. C., Sa, A. M. O., Vieira, P. C., Silva, E. R., & d. . (2016). Stachytarpheta cayennensis extract inhibits promastigote and amastigote growth in Leishmania amazonensis via parasitearginase inhibition. Journal of Ethnopharmacology, 192, 108–113. · DOI
  41. Chowdhury, R., Rashid, M. U., Khan, O. F., & Hasan, C. M. (2004). Bioactivity of extractives from Stachytarpheta urticaefolia. Pharmaceutical Biology, 42(3), 262–267. · DOI
  42. Calis, I., Kirmizibekmez, H., Ersoz, T., Saracoglu, I., Donmez, A. A., Mitova, M., Handjieva, N., & Popov, S. (2002). Iridoid, phenylethanoid and flavonoid glycosides from Phlomis sintenisii. Acta Pharmaceutica Turcica, 44(3), 195–203.
  43. Penido, C., Costa, K. A., Futuro, D. O., Paiva, S. R., Kaplan, M. A. C., Figueiredo, M. R., & Henriques, M. G. M. O. (2006). Anti-inflammatory and anti-ulcerogenic properties of Stachytarpheta cayennensis (L.C. Rich) Vahl. Journal of Ethnopharmacology, 104, 225–233. · DOI
  44. Viljoen, A., Mncwangi, N., & Vermaak, I. (2012). Anti-inflammatory iridoids of botanical origin. Current Medicinal Chemistry, 19, 2104–2127. · DOI
  45. Tantisewie, B., & Sticher, O. (1975). Isolation of ipolammide from Stachytarpheta Indica. Phytochemistry, 14, 1462–1463. · DOI
  46. Roengsumran, S., Sookkongwaree, K., Jaiboon, N., Chaichit, N., & Petsom, A. (2002). Crystal structure of ipolamiide monohydrate from Stachytarpheta indica. Analytical Sciences, 18(9), 1063–1064. · DOI
  47. Damtoft, S. (1981). Biosynthesis of lamiide and ipolamiide from 8-epi-deoxyloganin studied by 2H N.M.R. spectroscopy. Journal of the Chemical Society Chemical Communications, 5, 228–229. · DOI
  48. Andary, C., Wylde, R., Laffite, C., Privat, G., & Winternitz, F. (1982). Structures of verbascoside and orobanchoside, caffeic acid sugar esters from Orobanche rapum-genistae. Phytochemistry, 21(5), 1123–1127. · DOI
  49. Li, L., Tsao, R., Liu, Z., Liu, S., Yang, R., Young, J. C., Zhu, H., Deng, Z., Xie, M., & Fu, Z. (2005). Isolation and purification of acteoside and isoacteoside from Plantago psyllium L. by high-speed counter-current chromatography. Journal of Chromatography A, 1063, 161–169. · DOI
  50. Pereira, A. M. S., Hernandes, C., Pereira, S. I. V., Bertoni, B. W., Franca, S. C., Pereira, P. S., & Taleb-Contini, S. H. (2014). Evaluation of anticandidal and antioxidant activities of phenolic compounds from Pyrostegia venusta (Ker Gawl.) Miers. Chemico-Biological Interactions, 224, 136–141. · DOI
  51. Pettit, G. R., Numata, A., Takemura, T., Ode, R. H., Narula, A. S., Schmidt, J. M., Cragg, G. M., & Pase, C. P. (1990). Antineoplastic agents, 107. Isolation of acteoside and isoacteoside from castilleja linariaefolia. Journal of Natural Products, 53(2), 456–458. · DOI
  52. Alipieva, K., Korkina, L., Orhan, I. E., & Georgiev, M. I. (2014). Verbascoside — a review of its occurrence, (bio)synthesis and pharmacological significance. Biotechnology Advances, 32, 1065–1076. · DOI
  53. Shiao, Y.-J., Su, M.-H., Lin, H.-C., & Wu, C.-R. (2017). Acteoside and isoacteoside protect amyloid peptide induced cytotoxicity, cognitive deficit and neurochemical disturbances in vitro and in vivo. International Journal of Molecular Sciences, 18(4), 895. · DOI
  54. Chen, C., Zhao, X.-H., Yue, H.-L., Li, Y.-L., & Chen, T. (2014). Separation of phenylpropanoid glycosides from a Chinese herb by HSCCC. Journal of Chromatographic Science, 52, 395–399. · DOI
  55. Souza, P. A. D., Silva, C. G., Machado, B. R. P., d Lucas, N. C., Leitão, G. G., Eleutherio, E. C. A., Ortiz, G. M. D., & Benchetrit, L. C. (2010). Evaluation of antimicrobial, antioxidant and phototoxic activities of extracts and isolated compounds from Stachytarpheta cayennensis (Rich.) Vahl. Verbenaceae. Brazilian Journal of Pharmacognosy, 20(6), 922–928. · DOI
  56. Sitarek, P., Skała, E., Toma, M., Wielanek, M., Szemraj, J., Nieborowska-Skorska, M., Kolasa, M., Skorski, T., Wysokińska, H., & Śliwiński, T. (2016). A preliminary study of apoptosis induction in glioma cells via alteration of the Bax/Bcl-2-p53 axis by transformed and non-transformed root extracts of Leonurus sibiricus L. Tumor Biology, 37, 8753–8764. · DOI
  57. Vertuani, S., Beghelli, E., Scalambra, E., Malisardi, G., Copetti, S., Toso, R. D., Baldisserotto, A., & Manfredini, S. (2011). Activity and stability studies of verbascoside, a novel antioxidant, in dermo-cosmetic and pharmaceutical topical formulations. Molecules, 16, 7068–7080. · DOI
  58. Tang, K. S. C., Konczak, I., & Zhao, J. (2017). Phenolic compounds of the Australian native herb Prostanthera rotundifolia and their biological activities. Food Chemistry, 233, 530–539. · DOI
  59. Etemad, L., Zafari, R., Vahdati-Mashhadian, N., Moallem, S. A., Shirvan, Z. O., & Hosseinzadeh, H. (2015). Acute, sub-acute and cell toxicity of verbascoside. Research Journal of Medicinal Plant, 9(7), 354–360. · DOI
  60. Basch, H., & Gadebusch, H. H. (1968). In vitro antimicrobial activity of dimethylsulfoxide. Applied Microbiology, 16(12), 1953–1954. · DOI
  61. Cevallos, A. M., Herrera, J., & Hernandez, I.L.-V.R. (2017). Differential effects of two widely used solvents, DMSO and ethanol, on the growth and recovery of Trypanosoma cruzi Epimastigotes in Culture. Korean Journal of Parasitology, 55(1), 81–84. · DOI
  62. Kirkwood, Z. I., Millar, B. C., Downey, D. G., & Moore, J. E. (2018). Antimicrobial effect of dimethyl sulfoxide and N, N-dimethylformamide on Mycobacterium abscessus: Implications for antimicrobial susceptibility testing. International Journal of Mycobacteriology, 7(2), 134–136. · DOI
  63. Tortora, G. G., Funke, B. R. & Case, C. L. (2015) Microbiology: an introduction 12 ed, Pearson Publication.
  64. Willey, J. M., Sherwood, L. & Woolverton, C. (2007) Microbiology, 7 ed, McGraw-Hill Education.
  65. Rigano, D., Formisano, C., Basile, A., Lavitola, A., Senatore, F., Rosselli, S., & Bruno, M. (2007). Antibacterial activity of flavonoids and phenylpropanoids from Marrubium globosum ssp. libanoticum. Phytotherapy Research, 21, 395–397. · DOI
  66. Nazemiyeh, H., Rahman, M. M., Gibbons, S., Nahar, L., Delazar, A., Ghahramani, M.-A., Talebpour, A.-H., & Sarker, S. D. (2008). Assessment of the antibacterial activity of phenylethanoid glycosides from Phlomis lanceolata against multiple-drug-resistant strains of Staphylococcus aureus. Journal of Natural Medicines, 62, 91–95. · DOI
  67. Barnes, E. C., Kavanagh, A. M., Ramu, S., Blaskovich, M. A., Cooper, M. A., & Davis, R. A. (2013). Antibacterial serrulatane diterpenes from the Australian native plant Eremophila microtheca. Phytochemistry, 93, 162–169. · DOI
  68. Avila, J. G., d Liverant, J. G., Martınez, A., Martınez, G., Munoz, J. L., Arciniegas, A., & d Vivar, A. R. (1999). Mode of action of Buddleja cordata verbascoside against Staphylococcus aureus. Journal of Ethnopharmacology, 66(1), 75–78. · DOI
  69. Funes, L., Laporta, O., Cerdan-Calero, M., & Micol, V. (2010). Effects of verbascoside, a phenylpropanoid glycoside from lemon verbena, on phospholipid model membranes. Chemistry and Physics of Lipids, 163, 190–199. · DOI
  70. Han, L., & Yin, Z. (2018). Learning to transfermicroscopy image modalities. Machine Vision and Applications, 29, 1257–1267. · DOI
  71. Kirfel, G., & Herzog, V. (2004). Migration of epidermal keratinocytes: Mechanisms, regulation, and biological significance. Protoplasma, 223, 67–78. · DOI
  72. Kirfel, G., Borm, B., Rigort, A., & Herzog, V. (2002). The secretory β-amyloid precursor protein is a motogen for human epidermal keratinocytes. European Journal of Cell Biology, 81, 664–676. · DOI
  73. Hoffmann, J., Twiesselmann, C., Kummer, M. P., Romagnoli, P., & Herzog, V. (2000). A possible role for the Alzheimer amyloid precursor protien in the regulation of epidermal basal cell proliferation. European Journal of Cell Biology, 79, 905–914. · DOI
  74. Speranza, L., Franceschelli, S., Pesce, M., Reale, M., Menghini, L., Vinciguerra, I., Lutiis, M. A. D., Felaco, M., & Grilli, A. (2010). Antiinflammatory effects in THP-1 cells treated with verbascoside. Phytotherapy Research, 24, 1398–1404. · DOI
  75. Lee, J.-W., Seo, K.-H., Ryu, H. W., Yuk, H. J., Park, H. A., Lim, Y. R., Ahn, K.-S., & Oh, S.-R. (2018). Anti-inflammatory effect of stem bark of Paulownia tomentosa Steud. in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages and LPS induced murine model of acute lung injury. Journal of Ethnopharmacology, 210, 23–30. · DOI
  76. Kostyuk, V. A., Potapovich, A. I., Suhan, T. O., d Luca, C., & Korkina, L. G. (2011). Antioxidant and signal modulation properties of plant polyphenols in controlling vascular inflammation. European Journal of Pharmacology, 658, 248–256. · DOI
  77. Pastore, S., Lulli, D., Fidanza, P., Potapovich, A. I., Kostyuk, V. A., Luca, C. D., Chik, E. M., & Korkina, L. G. (2012). Plant polyphenols regulate chemokine expression and tissue repair in human keratinocytes through interaction with cytoplasmic and nuclear components of epidermal growth factor receptor system. Antioxidants and Redox Signaling, 16(4), 314–328. · DOI
  78. Georgiev, M., Pastore, S., Lulli, D., Alipieva, K., Kostyuk, V., Potapovich, A., Panetta, M., & Korkina, L. (2012). Verbascum xanthophoeniceum-derived phenyl ethanoid glycosides are potent inhibitors of inflammatory chemokines in dormant and interferon-gamma-stimulated human keratinocytes. Journal of Ethnopharmacology, 144, 754–760. · DOI
  79. Sperotto, N. D. D. M., Luiza, S., Rodrigo, M. V., Jeferson, G. H., Valeria, F. P., Priscila, V., Jose, A. B. C., Adriana, R., Jenifer, S., & Dinara, J. M. (2018). Wound healing and anti-inflammatory activities induced by a Plantago australis hydroethanolic extract standardized in verbascoside. Journal of Ethnopharmacology, 225, 178–188. · DOI
  80. Schapoval, E. E. S., d Vargas, M. R. W., Chaves, C. G., Bridi, R., Zuanazzi, J. A., & Henriques, A. T. (1998). Antiinflammatory and antinociceptive activities of extracts and isolated compounds from Stachytarpheta cayennensis. Journal of Ethnopharmacology, 60, 53–59. · DOI

Cited by

Metadata

Authors
Agampodi, V. A., Katavic, P., Collet, C., & Collet, T.
Affiliations
Queensland University of Technology (AU)
Corresponding author
Agampodi, Vajira Asela
Venue
Applied Biochemistry and Biotechnology
Published
2022-07-29
Volume
194
Issue
12
Pages
6213-6254
ISSN
  • 0273-2289 (ISSN-L)
  • 1559-0291
OpenAlex
W4288708362
Cited by
11
References
0
Citations by year
2026: 3 · 2024: 3 · 2023: 2 · 2022: 3
FWCI
0.87
Type
journal article
Language
en
Open access
Locations
  • Applied Biochemistry and Biotechnology (publishedVersion)
  • Research Square (acceptedVersion, cc-by)
  • PubMed (publishedVersion)
  • QUT ePrints (Queensland University of Technology) (submittedVersion, cc-by-nc)
Topics
  • Health Sciences › Medicine › Surgery › Wound Healing and Treatments
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry and Biological Activities
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry and biological activity of medicinal plants
Keywords
Stachytarpheta indica, wound healing, antibacterial activity, anti-inflammatory activity, leaf extract, verbascoside, keratinocyte proliferation, keratinocyte migration, cyclooxygenase inhibition, 5-lipoxygenase inhibition, interleukin-8, Staphylococcus, traditional medicine
MeSH terms
Anti-Inflammatory Agents, Anti-Bacterial Agents, Glucosides, Humans, Inflammation, Plant Extracts, Wound Healing, Plant Leaves, Polyphenols

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