Evidence map›Paper›PMID 26064051›Full record

ArticleNeuropsychiatric disease and treatment2015

Ranitidine reduced levodopa-induced dyskinesia by remodeling neurochemical changes in hemiparkinsonian model of rats.

Hongjuan Shi, Xinxin Yang, Hui Zhao, Shenyang Zhang, Jie Zu, Wei Zhang, Xia Shen, Guiyun Cui, Fang Hua, Chuanzhu Yan

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 97% 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

2 citing papers in PubMed, 5 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

10 authors at 3 institutions in 1 country.

Hongjuan ShiDepartment of Neurology, Qilu Hospital of Shangdong University, Jinan, People's Republic of China ; Department of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China.
Xinxin YangDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China ; Institute of Neurological Diseases of Xuzhou Medical College, Xuzhou, People's Republic of China.
Hui ZhaoDepartment of Neurology, Xuzhou Central Hospital, Xuzhou, People's Republic of China.
Shenyang ZhangDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China.
Jie ZuDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China.
Wei ZhangDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China.
Xia ShenDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China.
Guiyun CuiDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China ; Institute of Neurological Diseases of Xuzhou Medical College, Xuzhou, People's Republic of China.
Fang HuaDepartment of Neurology, Affiliated Hospital of Xuzhou Medical College, Xuzhou, People's Republic of China ; Institute of Neurological Diseases of Xuzhou Medical College, Xuzhou, People's Republic of China.
Chuanzhu YanDepartment of Neurology, Qilu Hospital of Shangdong University, Jinan, People's Republic of China.
Affiliated Hospital of Xuzhou Medical College · CNXuzhou Central Hospital · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLevodopa (l-dopa) remains the best drug in the treatment of Parkinson's disease (PD). Unfortunately, long-term l-dopa caused motor complications, one of which is l-dopa-induced dyskinesia (LID). The precise mechanisms of LID are not fully understood. We have previously reported that ranitidine could reduce LID by inhibiting the activity of protein kinase A pathway in a rat model of PD. It is demonstrated that neurotransmitters such as γ-aminobutyric-acid (GABA) and glutamate (Glu) are also involved in the expression of LID. But whether ranitidine could reduce LID by remodeling the neurochemical changes is unknown.

methodsIn the present study, we produced PD rats by injection of 6-hydroxydopamine. Then PD rats were treated with vehicle, l-dopa (6 mg/kg, plus benserazide 12 mg/kg, intraperitoneal [ip]) or l-dopa (6 mg/kg, plus benserazide 12 mg/kg, ip) plus ranitidine (10 mg/kg, oral). Abnormal voluntary movements were adopted to measure the antidyskinetic effect of ranitidine in PD rats. Rotarod tests were used to observe whether ranitidine treatment affects the antiparkinsonian effect of l-dopa. In vivo microdialysis was used to measure nigral GABA and striatal Glu in PD rats.

resultsWe found that ranitidine pretreatment reduced abnormal voluntary movements in l-dopa-primed PD rats without affecting the antiparkinsonian effect of l-dopa. In parallel with behavioral improvement, ranitidine pretreatment reduced protein kinase A activity and suppressed the surge of nigral GABA and striatal Glu.

conclusionThese data indicated that ranitidine could reduce LID by modeling neurochemical changes induced by l-dopa, suggesting a novel mechanism of ranitidine in the treatment of LID.

Indexed as

glutamatelevodopa-induced dyskinesiaParkinson’s diseasePKAranitidineγ-aminobutyric-acid

Identifiers

PMID26064051
PMCPMC4455849
OpenAlexW1706488456

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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.