Evidence map›Paper›PMID 36742263›Full record

ArticleClinical, cosmetic and investigational dermatology2023

Aloe Extracts Inhibit Skin Inflammatory Responses by Regulating NF-κB, ERK, and JNK Signaling Pathways in an LPS-Induced RAW264.7 Macrophages Model.

Fei Wang, Jitao Liu, Quan An, Yiming Wang, Yang Yang, Tong Huo, Simin Yang, Ruijun Ju, Qianghua Quan

Open access · goldAbstract read
In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 2023. 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
9.1field-weighted citation impact, top 3% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  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

9 authors at 2 institutions in 1 country.

Fei Wang *Research and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.
Jitao LiuResearch and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.
Quan An *Research and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.
Yiming WangResearch and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.
Yang YangResearch and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.
Tong HuoResearch and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.ORCID 0000-0003-4731-283X
Simin YangBeijing Key Laboratory of Enze Biomass Fine Chemicals, Department of Pharmaceutical Engineering, Beijing Institute of Petrochemical Technology, Beijing, People's Republic of China.
Ruijun JuBeijing Key Laboratory of Enze Biomass Fine Chemicals, Department of Pharmaceutical Engineering, Beijing Institute of Petrochemical Technology, Beijing, People's Republic of China.
Qianghua QuanResearch and Development Department, Yunnan Baiyao Group Health Products Co., Ltd., Kunming, People's Republic of China.
Sinovac Biotech · CNBeijing Institute of Petrochemical Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Inflammation generally refers to the body's defensive response to stimuli, and skin inflammation is still one of the major problems that affect human physical and mental health. While current pharmacological treatments are reported to have cytotoxicity and various side effects, herbal medicines with few side effects and low cytotoxicity are considered as alternative therapeutic approaches. Methods: In order to investigate anti-inflammatory effects and mechanisms of ALOE, the potential cytotoxicity of Results: ALOE did not exhibit obvious cytotoxicity (0-3 mg/mL) in vitro. ALOE was able to inhibit the expression of pro-inflammatory cytokines IL-6, TNF-α and functioned more prominently in LPS-induced model. ALOE could also suppress the mRNA expression of LPS-induced Conclusion: Taken together, these results demonstrated that ALOE is a potential treatment in suppressing LPS-stimulated inflammation reactions targeting NF-κB, JNK and ERK signaling pathways. The anti-inflammatory effects of ALOE indicated that it has the potential to become an effective cosmetic ingredient.

Indexed as

Aloe vera extractsanti-inflammationCOX-2iNOSLPSMAPKNF-κBNOP65

Identifiers

PMID36742263
PMCPMC9891070
OpenAlexW4318220204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.