Evidence map›Paper›PMID 12107094›Full record

ArticleThe American journal of pathology2002

Nicotine accelerates angiogenesis and wound healing in genetically diabetic mice.

Johannes Jacobi, James J Jang, Uma Sundram, Hayan Dayoub, Luis F Fajardo, John P Cooke

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 175 citations in OpenAlex.

  1. Article
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  5. Review
  6. The controversial effect of smoking and nicotine in SARS-CoV-2 infection.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2023
    Review
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  15. Topical nicotinic receptor activation improves wound bacterial infection outcomes and TLR2-mediated inflammation in diabetic mouse wounds.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2018
    Article
  16. Article
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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

6 authors at 1 institution in 1 country.

Johannes JacobiDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
James J Jang
Uma Sundram
Hayan Dayoub
Luis F Fajardo
John P Cooke
Stanford University · US

Funding

Stress, The HPA and Health in AgingP01AG018784 · NIA · STANFORD UNIVERSITY · PI SPIEGEL, DAVID · 2001 to 2008
$8.7M
Transplant Arteriosclerosis: Viral and Host MechanismP01AI050153 · NIAID · STANFORD UNIVERSITY · PI MOCARSKI, EDWARD S. · 2001 to 2005
$6.5M
Phase 2: NOs pathway in arterial diseaseR01HL063685 · NHLBI · STANFORD UNIVERSITY · PI COOKE, JOHN P · 2000 to 2004
$2.2M
NHLBI NIH HHS R01 HL00204NHLBI NIH HHS R01 HL063685NHLBI NIH HHS R01 HL-63685NIAID NIH HHS P01 AI050153NIAID NIH HHS P01AI50153NIA NIH HHS P01 AG018784NIA NIH HHS P01 AG18784
6 · The paper itself

Abstract

Recently, we have discovered an endogenous cholinergic pathway for angiogenesis mediated by endothelial nicotinic acetylcholine receptors (nAChRs). Since angiogenesis plays a major role in wound repair, we hypothesized that activation of nAChRs with nicotine would accelerate wound healing in a murine excisional wound model. In genetically diabetic and control mice full-thickness skin wounds (0.8 cm) were created on the dorsum and topically treated over 7 days with either vehicle (phosphate-buffered saline, PBS) or nicotine (10(-8) mol/L, 10(-9) mol/L; each, n = 5). Wound size was measured over 14 days followed by resection, histological analysis, and quantitation of vascularity. In diabetic animals an agonist (epibatidine, 10(-10) mol/L) or antagonist (hexamethonium, 10(-4) mol/L) of nAChRs as well as the positive control basic fibroblast growth factor (bFGF, 25 microg/kg) were also tested. To further study the role of endothelial nAChRs in angiogenesis, we used an ex vivo vascular explant model. In diabetic mice wound healing was markedly impaired. Nicotine significantly accelerated wound healing as assessed by closure rate and histological score. The effects of nicotine were equal to bFGF and were mimicked by epibatidine and blocked by hexamethonium. Histomorphometry revealed increased neovascularization in animals treated with nicotine. Furthermore, capillary-like sprouting from vascular explants was significantly enhanced by nicotine. In conclusion, agonist-induced stimulation of nAChRs accelerates wound healing in diabetic mice by promoting angiogenesis. We have discovered a cholinergic pathway for angiogenesis that is involved in wound healing, and which is a potential target for therapeutic angiogenesis.

Indexed as

AnimalsAorta, ThoracicBlood VesselsDiabetes Mellitus, Type 2In Vitro TechniquesMiceNeovascularization, PhysiologicNicotineNicotinic AgonistsReceptors, NicotinicTime FactorsWound HealingNicotineNicotinic AgonistsReceptors, Nicotinic

Identifiers

PMID12107094
PMCPMC1850685
OpenAlexW2169681172

What OpenQuestion holds

Textmetadata
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.