Crinum latifolium extract inhibits lipopolysaccharide-induced inflammation in human macrophages


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Kokturk S., ÇETİNKOL Y., CIRRIK S.

REVISTA ROMANA DE MEDICINA DE LABORATOR, vol.30, no.2, pp.183-190, 2022 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 30 Issue: 2
  • Publication Date: 2022
  • Doi Number: 10.2478/rrlm-2022-0015
  • Journal Name: REVISTA ROMANA DE MEDICINA DE LABORATOR
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), CAB Abstracts, Directory of Open Access Journals
  • Page Numbers: pp.183-190
  • Keywords: inflammation, macrophage, interleukin-6, Crinum latifolium extract, endosomes, ACTIVATION, DISEASE, HEALTH
  • Open Archive Collection: AVESIS Open Access Collection
  • Istanbul University Affiliated: Yes

Abstract

Introduction: Crinum latifolium is a natural plant showing the anti-inflammatory effects. We aimed to evaluate the effects of Crinum latifolium extract on proinflammatory cytokine production and maturation of early and late endosomes in the lipopolysaccharide (LPS)-induced human macrophages at light microscopic and biochemical levels. Material and Methods: The effects of Crinum latifolium extract in human macrophages stimulated with LPS was evaluated to optic densities of the lysosome-associated membrane protein-1 (LAMP-1) and early endo-some antigen 1 (EEA1) by immunohistochemistry staining and to level of the proinflammatory cytokine interleukin (IL)-6 by enzyme-linked immunosorbent assay (ELISA). Results: Crinum latifolium group exhibited a significant decreased in the levels of IL-6 in the supernatant as compared to the LPS group for 2 and 72 hours (p<0.0001). Crinum latifolium group exhibited a significant increased in the optic density of the EEA1 and LAMP-1 in coverslips as compared to the control and lipopolysaccharide groups after 2 and 72 hours (p<0.0001). Conclusions: Crinum latifolium may a therapeutic plant in the inflammatory diseases, such as sepsis, through anti-inflammatory effects, such as decrease in production of the proinflammatory cytokine and increase in maturations of the early and late endosomes in macrophages.