Evidence map›Paper›PMID 31638092›Full record

ArticleNeural regeneration research2020

Protective effects of organic extracts of

Li-Hong Duan, Meng Li, Chun-Bao Wang, Qing-Mei Wang, Quan-Quan Liu, Wan-Feng Shang, Ya-Jin Shen, Zhuo-Hua Lin, Tong-Yang Sun, Zheng-Zhi Wu and 3 more

Abstract read
In one paragraph

Article in Neural regeneration research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Antioxidant Capacity and Protective Effects on HFoods (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Pharmacological Mechanisms Underlying the Neuroprotective Effects ofInternational journal of molecular sciences · 2020
    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

13 authors.

Li-Hong DuanShenzhen Institute of Geriatrics; Department of Rehabilitation, the Second People's Hospital of Shenzhen; Stroke Biological Recovery Laboratory, Spaulding Rehabilitation Hospital, Harvard Medical School, Charlestown, MA, USA; Department of Mechanical and Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, China.
Meng LiShenzhen Institute of Geriatrics, Shenzhen, Guangdong Province, China.
Chun-Bao WangShenzhen Institute of Geriatrics; Department of Rehabilitation, the Second People's Hospital of Shenzhen; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University, Shenzhen; School of Mechanical and Automotive Engineering, South China University of Technology, Guangzhou, Guangdong Province; School of Mechanical Engineering, Guangxi University of Science and Technology, Liuzhou, Guangxi Zhuang Autonomous Region; Mingkai Smart Medical Robot Co., Ltd., Shenzhen, Guangdong Province, China.
Qing-Mei WangStroke Biological Recovery Laboratory, Spaulding Rehabilitation Hospital, Harvard Medical School, Charlestown, MA, USA.
Quan-Quan LiuShenzhen Institute of Geriatrics; Department of Rehabilitation, the Second People's Hospital of Shenzhen; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University; Mingkai Smart Medical Robot Co., Ltd., Shenzhen, Guangdong Province, China.
Wan-Feng ShangShenzhen Institute of Geriatrics; Department of Rehabilitation, the Second People's Hospital of Shenzhen; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, China.
Ya-Jin ShenDepartment of Mechanical and Biomedical Engineering, City University of Hong Kong, Hong Kong Special Administrative Region, China.
Zhuo-Hua LinMingkai Smart Medical Robot Co., Ltd., Shenzhen, Guangdong Province, China.
Tong-Yang SunSchool of Mechanical and Automotive Engineering, South China University of Technology, Guangzhou, Guangdong Province, China.
Zheng-Zhi WuShenzhen Institute of Geriatrics; Department of Rehabilitation, the Second People's Hospital of Shenzhen; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, China.
Ying-Hong LiShenzhen Institute of Geriatrics; Department of Rehabilitation, the Second People's Hospital of Shenzhen; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, China.
Yu-Long WangDepartment of Rehabilitation, the Second People's Hospital of Shenzhen; Department of Rehabilitation, the First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, China.
Xun LuoKerry Rehabilitation Medicine Research Institute, Shenzhen, Guangdong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alpinia oxyphylla, a traditional herb, is widely used for its neuroprotective, antioxidant and memory-improving effects. However, the neuroprotective mechanisms of action of its active ingredients are unclear. In this study, we investigated the neuroprotective effects of various organic extracts of Alpinia oxyphylla on PC12 cells exposed to hydrogen peroxide-induced oxidative injury in vitro. Alpinia oxyphylla was extracted three times with 95% ethanol (representing extracts 1-3). The third 95% ethanol extract was dried and resuspended in water, and then extracted successively with petroleum ether, ethyl acetate and n-butanol (representing extracts 4-6). The cell counting kit-8 assay and microscopy were used to evaluate cell viability and observe the morphology of PC12 cells. The protective effect of the three ethanol extracts (at tested concentrations of 50, 100 and 200 µg/mL) against cytotoxicity to PC12 cells increased in a concentration-dependent manner. The ethyl acetate, petroleum ether and n-butanol extracts (each tested at 100, 150 and 200 μg/mL) had neuroprotective effects as well. The optimum effective concentration ranged from 50-200 μg/mL, and the protective effect of the ethyl acetate extract was comparatively robust. These results demonstrate that organic extracts of Alpinia oxyphylla protect PC12 cells against apoptosis induced by hydrogen peroxide. Our findings should help identify the bioactive neuroprotective components in Alpinia oxyphylla.

Indexed as

active ingredientsAlpinia oxyphyllaapoptosisethanol crude extractfractionhydrogen peroxidenerve regenerationneuroprotective agentneuroprotective effectsPC12 cellstraditional herb

Identifiers

PMID31638092
PMCPMC6975140

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.