Evidence map›Paper›PMID 19433069›Full record

ReviewBiochemical pharmacology2009

Multiple roles for nicotine in Parkinson's disease.

Maryka Quik, Luping Z Huang, Neeraja Parameswaran, Tanuja Bordia, Carla Campos, Xiomara A Perez

Open access · greenAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.6field-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

55 citing papers in PubMed, 135 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Phytochemicals derived fromFrontiers in pharmacology · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Life style and Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Maryka QuikThe Parkinson's Institute, Sunnyvale, CA 94085, United States. mquik@parkinsonsinstitute.org
Luping Z Huang
Neeraja Parameswaran
Tanuja Bordia
Carla Campos
Xiomara A Perez
Parkinson's Institute and Clinical Center · US

Funding

Nicotinic Receptors in Parkinson's DiseaseR01NS042091 · NINDS · SRI INTERNATIONAL · PI QUIK, MARYKA · 2003 to 2007
$1.6M
Nicotinic and neuroprotection in a parkinson mouse modelR01NS047162 · NINDS · SRI INTERNATIONAL · PI QUIK, MARYKA · 2004 to 2007
$1.1M
NINDS NIH HHS NS42091NINDS NIH HHS NS47162NINDS NIH HHS R01 NS042091NINDS NIH HHS R01 NS047162
6 · The paper itself

Abstract

There exists a remarkable diversity of neurotransmitter compounds in the striatum, a pivotal brain region in the pathology of Parkinson's disease, a movement disorder characterized by rigidity, tremor and bradykinesia. The striatal dopaminergic system, which is particularly vulnerable to neurodegeneration in this disorder, appears to be the major contributor to these motor problems. However, numerous other neurotransmitter systems in the striatum most likely also play a significant role, including the nicotinic cholinergic system. Indeed, there is an extensive anatomical overlap between dopaminergic and cholinergic neurons, and acetylcholine is well known to modulate striatal dopamine release both in vitro and in vivo. Nicotine, a drug that stimulates nicotinic acetylcholine receptors (nAChRs), influences several functions relevant to Parkinson's disease. Extensive studies in parkinsonian animals show that nicotine protects against nigrostriatal damage, findings that may explain the well-established decline in Parkinson's disease incidence with tobacco use. In addition, recent work shows that nicotine reduces l-dopa-induced abnormal involuntary movements, a debilitating complication of l-dopa therapy for Parkinson's disease. These combined observations suggest that nAChR stimulation may represent a useful treatment strategy for Parkinson's disease for neuroprotection and symptomatic treatment. Importantly, only selective nAChR subtypes are present in the striatum including the alpha4beta2*, alpha6beta2* and alpha7 nAChR populations. Treatment with nAChR ligands directed to these subtypes may thus yield optimal therapeutic benefit for Parkinson's disease, with a minimum of adverse side effects.

Indexed as

AnimalsAntiparkinson AgentsCorpus StriatumHumansLevodopaMotor SkillsNeuroprotective AgentsNicotineNicotinic AgonistsParkinson DiseaseReceptors, NicotinicSmokingSubstantia NigraAntiparkinson AgentsLevodopaNeuroprotective AgentsNicotineNicotinic AgonistsReceptors, Nicotinic

Identifiers

PMID19433069
PMCPMC2815339
OpenAlexW2042668530

What OpenQuestion holds

Textmetadata
LicenceTDM
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.