Effects of Mitragyna speciosa (Korth.) on macrophage immune responses

Mitragyna Speciosa (Korth.) or Kratom is an Asian tropical plant that exhibits medicinal benefits, including antioxidants, antibacterial, and antinociceptive effects. This study aimed to explore the immunomodulatory effect of M. speciosa methanolic extract (MSME) on peritoneal isolated primary macro...

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Main Authors: Kafo, Anwar S K, M Elsalami, Rabia, Fatin Z Zailan, Nur, Mahayidin, Hasni, Ramasamy, Rajesh, H Zaidan, Uswatun, Hassan, Masriana
Format: Article
Published: EManuscript Technologies 2023
Online Access:http://psasir.upm.edu.my/id/eprint/107598/
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author Kafo, Anwar S K
M Elsalami, Rabia
Fatin Z Zailan, Nur
Mahayidin, Hasni
Ramasamy, Rajesh
H Zaidan, Uswatun
Hassan, Masriana
author_facet Kafo, Anwar S K
M Elsalami, Rabia
Fatin Z Zailan, Nur
Mahayidin, Hasni
Ramasamy, Rajesh
H Zaidan, Uswatun
Hassan, Masriana
author_sort Kafo, Anwar S K
building UPM Institutional Repository
collection Online Access
description Mitragyna Speciosa (Korth.) or Kratom is an Asian tropical plant that exhibits medicinal benefits, including antioxidants, antibacterial, and antinociceptive effects. This study aimed to explore the immunomodulatory effect of M. speciosa methanolic extract (MSME) on peritoneal isolated primary macrophages (pMø) and murine-derived macrophages, RAW264.7 cell line. The cytotoxicity effect of MSME on both RAW264.7 cells and pMø was determined by a cell viability test using a Cell-Titer Blue assay. Furthermore, the effects of MSME on the secretion and expression of mediators of the immune system, including nitric oxide (NO), inducible nitric oxide synthase (iNOS), and cytokines in lipopolysaccharide (LPS)- stimulated macrophages were evaluated by Griess assay and quantitative reverse transcription polymerase chain reaction (qRTPCR). In addition, the effect of MSME on the phagocytic activity of LPS-stimulated macrophages was determined by a neutral red uptake assay. The cytotoxicity analysis shows stable cell viability above 80% except when treated at a high MSME concentration (>100 µg/ml). MSME exhibited antiinflammatory effects in LPS-stimulated macrophages, as shown by a significant inhibition of NO secretion and the expression of iNOS, Tumor necrosis factor alpha (TNFα), Interleukin-1 beta (IL-1β), and Interleukin-6 (IL-6). Furthermore, the extract also significantly reduced the phagocytic capacity of both LPS-stimulated RAW264.7 cells (36.71±6.46; MSME 100 ug/mL; p=0.0266) and pMø (42.76±10.18%; MSME 10µg/mL; p=0.0142). In conclusion, our findings suggest that treatment of MSME in LPS-activated macrophage attenuated immune responses through inhibition of phagocytic ability, reduction of NO and iNOS levels, and downregulation of TNF-α, IL-1β, and IL-6 gene expression.
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spelling upm-1075982024-09-02T02:48:32Z http://psasir.upm.edu.my/id/eprint/107598/ Effects of Mitragyna speciosa (Korth.) on macrophage immune responses Kafo, Anwar S K M Elsalami, Rabia Fatin Z Zailan, Nur Mahayidin, Hasni Ramasamy, Rajesh H Zaidan, Uswatun Hassan, Masriana Mitragyna Speciosa (Korth.) or Kratom is an Asian tropical plant that exhibits medicinal benefits, including antioxidants, antibacterial, and antinociceptive effects. This study aimed to explore the immunomodulatory effect of M. speciosa methanolic extract (MSME) on peritoneal isolated primary macrophages (pMø) and murine-derived macrophages, RAW264.7 cell line. The cytotoxicity effect of MSME on both RAW264.7 cells and pMø was determined by a cell viability test using a Cell-Titer Blue assay. Furthermore, the effects of MSME on the secretion and expression of mediators of the immune system, including nitric oxide (NO), inducible nitric oxide synthase (iNOS), and cytokines in lipopolysaccharide (LPS)- stimulated macrophages were evaluated by Griess assay and quantitative reverse transcription polymerase chain reaction (qRTPCR). In addition, the effect of MSME on the phagocytic activity of LPS-stimulated macrophages was determined by a neutral red uptake assay. The cytotoxicity analysis shows stable cell viability above 80% except when treated at a high MSME concentration (>100 µg/ml). MSME exhibited antiinflammatory effects in LPS-stimulated macrophages, as shown by a significant inhibition of NO secretion and the expression of iNOS, Tumor necrosis factor alpha (TNFα), Interleukin-1 beta (IL-1β), and Interleukin-6 (IL-6). Furthermore, the extract also significantly reduced the phagocytic capacity of both LPS-stimulated RAW264.7 cells (36.71±6.46; MSME 100 ug/mL; p=0.0266) and pMø (42.76±10.18%; MSME 10µg/mL; p=0.0142). In conclusion, our findings suggest that treatment of MSME in LPS-activated macrophage attenuated immune responses through inhibition of phagocytic ability, reduction of NO and iNOS levels, and downregulation of TNF-α, IL-1β, and IL-6 gene expression. EManuscript Technologies 2023-12-13 Article PeerReviewed Kafo, Anwar S K and M Elsalami, Rabia and Fatin Z Zailan, Nur and Mahayidin, Hasni and Ramasamy, Rajesh and H Zaidan, Uswatun and Hassan, Masriana (2023) Effects of Mitragyna speciosa (Korth.) on macrophage immune responses. Current Trends in Biotechnology and Pharmacy, 17 (4A). pp. 121-130. ISSN 0973-8916,2230-7303 https://abap.co.in/index.php/home/article/view/1205 10.5530/ctbp.2023.4s.99
spellingShingle Kafo, Anwar S K
M Elsalami, Rabia
Fatin Z Zailan, Nur
Mahayidin, Hasni
Ramasamy, Rajesh
H Zaidan, Uswatun
Hassan, Masriana
Effects of Mitragyna speciosa (Korth.) on macrophage immune responses
title Effects of Mitragyna speciosa (Korth.) on macrophage immune responses
title_full Effects of Mitragyna speciosa (Korth.) on macrophage immune responses
title_fullStr Effects of Mitragyna speciosa (Korth.) on macrophage immune responses
title_full_unstemmed Effects of Mitragyna speciosa (Korth.) on macrophage immune responses
title_short Effects of Mitragyna speciosa (Korth.) on macrophage immune responses
title_sort effects of mitragyna speciosa (korth.) on macrophage immune responses
url http://psasir.upm.edu.my/id/eprint/107598/
http://psasir.upm.edu.my/id/eprint/107598/
http://psasir.upm.edu.my/id/eprint/107598/