Evidence map›Paper›PMID 25897205›Full record

ArticleDrug design, development and therapy2015

Gelatin nanoparticle-mediated intranasal delivery of substance P protects against 6-hydroxydopamine-induced apoptosis: an in vitro and in vivo study.

Cui-Tao Lu, Rong-Rong Jin, Yi-Na Jiang, Qian Lin, Wen-Ze Yu, Kai-Li Mao, Fu-Rong Tian, Ya-Ping Zhao, Ying-Zheng Zhao

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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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

9 authors at 1 institution in 1 country.

Cui-Tao LuThe Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, People's Republic of China ; School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Rong-Rong JinSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Yi-Na JiangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Qian LinSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Wen-Ze YuSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Kai-Li MaoSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Fu-Rong TianSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Ya-Ping ZhaoThe Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, People's Republic of China.
Ying-Zheng ZhaoSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, People's Republic of China.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to investigate the protective role of intranasally administered substance P-loaded gelatin nanoparticles (SP-GNPs) against 6-hydroxydopamine (6-OHDA)-induced apoptosis in vitro and in vivo, and to provide a new strategy for treating brain pathology, such as Parkinson's disease.

methodsSP-GNPs were prepared by a water-in-water emulsion method, and their stability, encapsulating efficiency, and loading capacity were evaluated. PC-12 cells were used to examine the enhancement of growth and inhibition of apoptosis by SP-GNPs in vitro using MTT assays. In the in vivo study, hemiparkinsonian rats were created by intracerebroventricular injection of 6-OHDA. The rats then received intranasal SP-GNPs daily for 2 weeks. Functional improvement was assessed by quantifying rotational behavior, and the degree of apoptosis was assessed by immunohistochemical staining for caspase-3 in the substantia nigra region.

resultsPC-12 cells with 6-OHDA-induced disease treated with SP-GNPs showed higher cell viability than their untreated counterparts, and cell viability increased as the concentration of substance P (SP) increased, indicating that SP could enhance cell growth and inhibit the cell apoptosis induced by 6-OHDA. Rats with 6-OHDA-induced hemiparkinsonism treated with SP-GNPs made fewer rotations and showed less staining for caspase-3 than their counterparts not treated with SP, indicating that SP protects rats with 6-OHDA-induced hemiparkinsonism from apoptosis and therefore demonstrates their functional improvement.

conclusionIntranasal delivery of SP-GNPs protects against 6-OHDA-induced apoptosis both in vitro and in vivo.

Indexed as

Drug Delivery SystemsAdministration, IntranasalAnimalsApoptosisCaspase 3Cells, CulturedDisease Models, AnimalGelatinMaleMolecular StructureNanoparticlesOxidopaminePC12 CellsRatsRats, Sprague-DawleyStructure-Activity RelationshipCaspase 3GelatinOxidopamineSubstance P6-hydroxydopamineapoptosisgelatin nanoparticlesintranasal deliveryParkinson’s diseasesubstance P

Identifiers

PMID25897205
PMCPMC4396575
OpenAlexW1985214422

What OpenQuestion holds

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Registered trials

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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.