Evidence map›Paper›PMID 37687125›Full record

ArticleMolecules (Basel, Switzerland)2023

Rutaecarpine Ameliorates Murine N-Methyl-N'-Nitro-N-Nitrosoguanidine-Induced Chronic Atrophic Gastritis by Sonic Hedgehog Pathway.

Yong He, Hong-Hong Liu, Xue-Lin Zhou, Ting-Ting He, Ao-Zhe Zhang, Xin Wang, Shi-Zhang Wei, Hao-Tian Li, Li-Sheng Chen, Lei Chang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

12 authors at 4 institutions in 1 country.

Yong HeSchool of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
Hong-Hong LiuDepartment of Pharmacy, Chinese PLA General Hospital, Beijing 100039, China.
Xue-Lin ZhouDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing 100039, China.
Ting-Ting HeDepartment of Pharmacy, Chinese PLA General Hospital, Beijing 100039, China.
Ao-Zhe ZhangDepartment of Pharmacy, Chinese PLA General Hospital, Beijing 100039, China.
Xin WangSchool of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
Shi-Zhang WeiDepartment of Pharmacy, Chinese PLA General Hospital, Beijing 100039, China.
Hao-Tian LiDepartment of Pharmacy, Chinese PLA General Hospital, Beijing 100039, China.
Li-Sheng ChenSchool of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.ORCID 0000-0003-3308-0898
Lei ChangSchool of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
Yan-Ling ZhaoSchool of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China.
Man-Yi JingDepartment of Pharmacy, Chinese PLA General Hospital, Beijing 100039, China.
Chinese PLA General Hospital · CNChengdu University of Traditional Chinese Medicine · CNCapital Medical University · CNSouthern Medical University · CN

Funding

Major Program of the National Natural Science Foundation of China No. 82192915
6 · The paper itself

Abstract

CAG is a burdensome and progressive disease. Numerous studies have shown the effectiveness of RUT in digestive system diseases. The therapeutic effects of RUT on MNNG-induced CAG and the potential mechanisms were probed. MNNG administration was employed to establish a CAG model. The HE and ELISA methods were applied to detect the treatment effects. WB, qRT-PCR, immunohistochemistry, TUNEL, and GES-1 cell flow cytometry approaches were employed to probe the mechanisms. The CAG model was successfully established. The ELISA and HE staining data showed that the RUT treatment effects on CAG rats were reflected by the amelioration of histological damage. The qRT-PCR and WB analyses indicated that the protective effect of RUT is related to the upregulation of the SHH pathway and downregulation of the downstream of apoptosis to improve gastric cellular survival. Our data suggest that RUT induces a gastroprotective effect by upregulating the SHH signaling pathway and stimulating anti-apoptosis downstream.

Indexed as

Gastritis, AtrophicHedgehog ProteinsAnimalsIndole AlkaloidsMethylnitronitrosoguanidineMiceNitrosoguanidinesQuinazolinesQuinazolinonesRatsSignal TransductionHedgehog ProteinsIndole AlkaloidsMethylnitronitrosoguanidineNitrosoguanidinesQuinazolinesQuinazolinonesrutecarpineapoptosischronic atrophic gastritisflow cytometryIL-1βrutaecarpineSHH signaling pathway

Identifiers

PMID37687125
PMCPMC10489734
OpenAlexW4386251032

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.