Evidence map›Paper›PMID 28836188›Full record

ArticleNeurotoxicity research2018

Heme Oxygenase-1-Inducing Activity of 4-Methoxydalbergione and 4'-Hydroxy-4-methoxydalbergione from Dalbergia odorifera and Their Anti-inflammatory and Cytoprotective Effects in Murine Hippocampal and BV2 Microglial Cell Line and Primary Rat Microglial Cells.

Dong-Cheol Kim, Dong-Sung Lee, Wonmin Ko, Kwan-Woo Kim, Hye Jin Kim, Chi-Su Yoon, Hyuncheol Oh, Youn-Chul Kim

Abstract read
PubMed Publisher
In one paragraph

Article in Neurotoxicity research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Chemical Analysis of the Ingredients of 20% Aqueous Ethanol Extract ofEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  6. Review
  7. Neuroprotective and Anti-Inflammatory Effects of Kuwanon C fromInternational journal of molecular sciences · 2020
    Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Dong-Cheol KimCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea.
Dong-Sung LeeCollege of Pharmacy, Chosun University, Dong-gu, Gwangju, 61452, Republic of Korea.
Wonmin KoCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea.
Kwan-Woo KimCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea.
Hye Jin KimCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea.
Chi-Su YoonCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea.
Hyuncheol OhCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea.
Youn-Chul KimCollege of Pharmacy, Wonkwang University, Iksan, 54538, Republic of Korea. yckim@wonkwang.ac.kr.
Wonkwang University · KRChosun University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dalbergia odorifera T. Chen (Leguminosae) grows in Central and South America, Africa, Madagascar, and Southern Asia. D. odorifera possesses many useful pharmacological properties, such as antioxidative and anti-inflammatory activities in various cell types. 4-Methoxydalbergione (MTD) and 4'-hydroxy-4-methoxydalbergione (HMTD) were isolated from the EtOH extract of D. odorifera by several chromatography methods. The chemical structures were elucidated by nuclear magnetic resonance (NMR) and mass spectrum (MS). Anti-inflammatory and cytoprotective effects were examined using BV2 microglial cells and murine hippocampus. MTD and HMTD were demonstrated to induce heme oxygenase (HO)-1 protein levels through the nuclear translocation of nuclear factor E2-related factor 2 (Nrf2) in BV2 microglial cells, while only MTD upregulated HO-1 in HT22 cells. MTD and HMTD induced HO-1 expression through JNK MAPK pathway in BV2 cells, whereas only MTD activated the ERK and p38 pathways in HT22 cells. MTD was also shown to activated MTD and HMTD suppressed lipopolysaccharide-stimulated nitric oxide (NO) and prostaglandin E2 production by inhibiting inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2) expression in a dose-dependent manner. Furthermore, MTD and HMTD attenuated pro-inflammatory cytokine productions. These anti-inflammatory effects were found to be mediated through the nuclear factor-kappa B (NF-κB) pathway. MTD exhibited neuroprotective effects on glutamate-induced neurotoxicity by promoting HO-1 in HT22 cells. The anti-inflammatory and cytoprotective effects of MTD and HMTD were partially reversed by an HO inhibitor tin protoporphyrin IX. In addition, MTD and HMTD inhibited pro-inflammatory cytokines and NF-κB pathway in primary rat microglia. These findings suggest that MTD and HMTD have therapeutic potential against neurodegenerative diseases accompanied by microglial activation and/or oxidative cellular injury.

Indexed as

AnimalsAnti-Inflammatory AgentsBenzoquinonesCell LineDalbergiaHeme Oxygenase-1HippocampusLipopolysaccharidesMicrogliaNeuroprotective AgentsNitric Oxide Synthase Type IIRats4-methoxydalbergioneAnti-Inflammatory AgentsBenzoquinonesHeme Oxygenase-1LipopolysaccharidesNeuroprotective AgentsNitric Oxide Synthase Type II4’-Hydroxy-4-methoxydalbergione4-MethoxydalbergioneHeme oxygenase-1Mitogen-activated protein kinaseNeuroinflammationNuclear factor-κB

Identifiers

PMID28836188
OpenAlexW2749837335

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.