PMID- 33671522 OWN - NLM STAT- MEDLINE DCOM- 20210407 LR - 20210407 IS - 1420-3049 (Electronic) IS - 1420-3049 (Linking) VI - 26 IP - 4 DP - 2021 Feb 22 TI - The Effects of New Zealand Grown Ginseng Fractions on Cytokine Production from Human Monocytic THP-1 Cells. LID - 10.3390/molecules26041158 [doi] LID - 1158 AB - Pro-inflammatory cytokines and anti-inflammatory cytokines are important mediators that regulate the inflammatory response in inflammation-related diseases. The aim of this study is to evaluate different New Zealand (NZ)-grown ginseng fractions on the productions of pro-inflammatory and anti-inflammatory cytokines in human monocytic THP-1 cells. Four NZ-grown ginseng fractions, including total ginseng extract (TGE), non-ginsenoside fraction extract (NGE), high-polar ginsenoside fraction extract (HPG), and less-polar ginsenoside fraction extract (LPG), were prepared and the ginsenoside compositions of extracts were analyzed by HPLC using 19 ginsenoside reference standards. The THP-1 cells were pre-treated with different concentrations of TGE, NGE, HPG, and LPG, and were then stimulated with lipopolysaccharide (LPS). The levels of pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1beta), interleukin-6 (IL-6), interleukin-8 (IL-8), and anti-inflammatory cytokines, such as interleukin-10 (IL-10), and transforming growth factor beta-1 (TGF-beta1), were determined by enzyme-linked immunosorbent assay (ELISA). TGE at 400 microg/mL significantly inhibited LPS-induced TNF-alpha and IL-6 productions. NGE did not show any effects on inflammatory secretion except inhibited IL-6 production at a high dose. Furthermore, LPG displayed a stronger effect than HPG on inhibiting pro-inflammatory cytokine (TNF-alpha, IL-1beta, and IL-6) productions. Particularly, 100 microg/mL LPG not only significantly inhibited the production of pro-inflammatory cytokines TNF-alpha, IL-1beta, and IL-6, but also remarkably enhanced the production of anti-inflammatory cytokine IL-10. NZ-grown ginseng exhibited anti-inflammatory effects in vitro, which is mainly attributed to ginsenoside fractions (particularly less-polar ginsenosides) rather than non-saponin fractions. FAU - Chen, Wei AU - Chen W AUID- ORCID: 0000-0001-7415-641X AD - School of Food and Advanced Technology, Massey University, Palmerston North 4442, New Zealand. AD - Riddet Institute, Massey University, Palmerston North 4442, New Zealand. AD - Alpha-Massey Natural Nutraceutical Research Centre, Massey University, Palmerston North 4442, New Zealand. FAU - Balan, Prabhu AU - Balan P AUID- ORCID: 0000-0003-0540-1471 AD - Riddet Institute, Massey University, Palmerston North 4442, New Zealand. AD - Alpha-Massey Natural Nutraceutical Research Centre, Massey University, Palmerston North 4442, New Zealand. FAU - Popovich, David G AU - Popovich DG AUID- ORCID: 0000-0002-8630-320X AD - School of Food and Advanced Technology, Massey University, Palmerston North 4442, New Zealand. LA - eng GR - RM18873/the Alpha-Massey Natural Nutraceutical Research Centre/ PT - Journal Article DEP - 20210222 PL - Switzerland TA - Molecules JT - Molecules (Basel, Switzerland) JID - 100964009 RN - 0 (Cytokines) RN - 0 (Ginsenosides) RN - 0 (Lipopolysaccharides) RN - 0 (Plant Extracts) SB - IM MH - Cytokines/analysis/*antagonists & inhibitors/biosynthesis MH - Dose-Response Relationship, Drug MH - Enzyme-Linked Immunosorbent Assay MH - Ginsenosides/chemistry/isolation & purification/*pharmacology MH - Humans MH - Lipopolysaccharides/antagonists & inhibitors/pharmacology MH - Panax/*chemistry MH - Plant Extracts/chemistry/isolation & purification/*pharmacology MH - THP-1 Cells PMC - PMC7926829 OTO - NOTNLM OT - NZ-grown ginseng OT - Panax ginseng OT - anti-inflammatory OT - less-polar ginsenosides OT - pro-inflammatory OT - saponins COIS- The authors declare no conflict of interest. EDAT- 2021/03/07 06:00 MHDA- 2021/04/10 06:00 PMCR- 2021/02/22 CRDT- 2021/03/06 01:10 PHST- 2021/02/05 00:00 [received] PHST- 2021/02/18 00:00 [revised] PHST- 2021/02/19 00:00 [accepted] PHST- 2021/03/06 01:10 [entrez] PHST- 2021/03/07 06:00 [pubmed] PHST- 2021/04/10 06:00 [medline] PHST- 2021/02/22 00:00 [pmc-release] AID - molecules26041158 [pii] AID - molecules-26-01158 [pii] AID - 10.3390/molecules26041158 [doi] PST - epublish SO - Molecules. 2021 Feb 22;26(4):1158. doi: 10.3390/molecules26041158.