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Nano-curcumin therapy,a promising method in modulating inflammatory cytokines in COVID-19 patients
Affiliation:1. Tuberculosis and Lung Disease Research Center of Tabriz University of Medical Sciences, Tabriz, Iran;2. Department of Internal Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran;3. Student’s Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran;4. Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran;5. Department of propaedeutics of dental diseases, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia;6. Department of Family Medicine, Yassawi International Kazakh-Turkish University Hospital, Turkistan, Kazakhstan;7. Department of Surgery, Mousavi Hospital, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran;8. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran;9. Cancer Gene Therapy Research Center (CGRC), Zanjan University of Medical Sciences, Zanjan, Iran
Abstract:BackgroundAs an ongoing worldwide health issue, Coronavirus disease 2019 (COVID–19) has been causing serious complications, including pneumonia, acute respiratory distress syndrome (ARDS), and multi-organ failure. However, there is no decisive treatment approach available for this disorder, which is primarily attributed to the large amount of inflammatory cytokine production. We aimed to identify the effects of Nano-curcumin on the modulation of inflammatory cytokines in COVID-19 patients.MethodForty COVID-19 patients and 40 healthy controls were recruited and evaluated for inflammatory cytokine expression and secretion. Subsequently, COVID-19 patients were divided into two groups: 20 patients receiving Nano-curcumin and 20 patients as the placebo group. The mRNA expression and cytokine secretion levels of IL-1β, IL-6, TNF-α and IL‐18 were assessed by Real‐time PCR and ELISA, respectively.ResultOur primary results indicated that the mRNA expression and cytokine secretion of IL-1β, IL-6, TNF-α, and IL-18 were increased significantly in COVID-19 patients compared with healthy control group. After treatment with Nano-curcumin, a significant decrease in IL-6 expression and secretion in serum and in supernatant (P = 0.0003, 0.0038, and 0.0001, respectively) and IL-1β gene expression and secretion level in serum and supernatant (P = 0.0017, 0.0082, and 0.0041, respectively) was observed. However, IL-18 mRNA expression and TNF-α concentration were not influenced by Nano-curcumin.ConclusionNano-curcumin, as an anti-inflammatory herbal based agent, may be able to modulate the increased rate of inflammatory cytokines especially IL-1β and IL-6 mRNA expression and cytokine secretion in COVID-19 patients, which may cause an improvement in clinical manifestation and overall recovery.
Keywords:COVID-19  Nano-curcumin  Cytokine storm  IL-1β  IL-6  ARDS"}  {"#name":"keyword"  "$":{"id":"k0035"}  "$$":[{"#name":"text"  "_":"acute respiratory distress syndrome  COVID-19"}  {"#name":"keyword"  "$":{"id":"k0045"}  "$$":[{"#name":"text"  "_":"Coronavirus disease 2019  SARS-CoV"}  {"#name":"keyword"  "$":{"id":"k0055"}  "$$":[{"#name":"text"  "_":"severe acute respiratory syndrome-CoV  MERS-CoV"}  {"#name":"keyword"  "$":{"id":"k0065"}  "$$":[{"#name":"text"  "_":"middle east respiratory syndrome-CoV  PBMCs"}  {"#name":"keyword"  "$":{"id":"k0075"}  "$$":[{"#name":"text"  "_":"peripheral blood mononuclear cells  ICU"}  {"#name":"keyword"  "$":{"id":"k0085"}  "$$":[{"#name":"text"  "_":"intensive care unit  IL-1β"}  {"#name":"keyword"  "$":{"id":"k0095"}  "$$":[{"#name":"text"  "_":"Interleukin-1 β  IL-6"}  {"#name":"keyword"  "$":{"id":"k0105"}  "$$":[{"#name":"text"  "_":"Interleukin-6  IL-7"}  {"#name":"keyword"  "$":{"id":"k0115"}  "$$":[{"#name":"text"  "_":"Interleukin_7  IL-8"}  {"#name":"keyword"  "$":{"id":"k0125"}  "$$":[{"#name":"text"  "_":"Interleukin-8  IL-18"}  {"#name":"keyword"  "$":{"id":"k0135"}  "$$":[{"#name":"text"  "_":"Interleukin-18  TNF-α"}  {"#name":"keyword"  "$":{"id":"k0145"}  "$$":[{"#name":"text"  "_":"tumor necrosis factor-alpha  MCP-1"}  {"#name":"keyword"  "$":{"id":"k0155"}  "$$":[{"#name":"text"  "_":"monocyte chemoattractant peptide  G-CSF"}  {"#name":"keyword"  "$":{"id":"k0165"}  "$$":[{"#name":"text"  "_":"granulocyte-colony stimulating factor  TLR"}  {"#name":"keyword"  "$":{"id":"k0175"}  "$$":[{"#name":"text"  "_":"toll-like receptors  CD80"}  {"#name":"keyword"  "$":{"id":"k0185"}  "$$":[{"#name":"text"  "_":"cluster of differentiation 80  CD86"}  {"#name":"keyword"  "$":{"id":"k0195"}  "$$":[{"#name":"text"  "_":"cluster of differentiation 86  ROS"}  {"#name":"keyword"  "$":{"id":"k0205"}  "$$":[{"#name":"text"  "_":"reactive oxygen species  PCR"}  {"#name":"keyword"  "$":{"id":"k0215"}  "$$":[{"#name":"text"  "_":"polymerase chain reaction  PBS"}  {"#name":"keyword"  "$":{"id":"k0225"}  "$$":[{"#name":"text"  "_":"phosphate buffered saline  FCS"}  {"#name":"keyword"  "$":{"id":"k0235"}  "$$":[{"#name":"text"  "_":"fetal calf serum  PMA"}  {"#name":"keyword"  "$":{"id":"k0245"}  "$$":[{"#name":"text"  "_":"phorbol myristate acetate  ELISA"}  {"#name":"keyword"  "$":{"id":"k0255"}  "$$":[{"#name":"text"  "_":"enzyme-linked immunosorbent assay  mRNA"}  {"#name":"keyword"  "$":{"id":"k0265"}  "$$":[{"#name":"text"  "_":"messenger RNA  cDNA"}  {"#name":"keyword"  "$":{"id":"k0275"}  "$$":[{"#name":"text"  "_":"complementary DNA  TMB"}  {"#name":"keyword"  "$":{"id":"k0285"}  "$$":[{"#name":"text"  "_":"tetra methyl benzidine  Th1"}  {"#name":"keyword"  "$":{"id":"k0295"}  "$$":[{"#name":"text"  "_":"T-helper-1  IBD"}  {"#name":"keyword"  "$":{"id":"k0305"}  "$$":[{"#name":"text"  "_":"inflammatory bowel disease  MS"}  {"#name":"keyword"  "$":{"id":"k0315"}  "$$":[{"#name":"text"  "_":"multiple sclerosis
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