Evidence map›Paper›PMID 35821897›Full record

ReviewPeerJ2022

The expanding roles of neuronal nitric oxide synthase (NOS1).

Kundan Solanki, Sajjan Rajpoot, Evgeny E Bezsonov, Alexander N Orekhov, Rohit Saluja, Anita Wary, Cassondra Axen, Kishore Wary, Mirza S Baig

Open access · goldAbstract readReview
In one paragraph

Review in PeerJ, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  6. Atractylenolide I mitigates Alzheimer's disease pathology in ApoEActa biochimica et biophysica Sinica · 2026
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  7. DifferentialScience advances · 2026
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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 5 institutions in 3 countries.

Kundan Solanki *Department of Biosciences and Biomedical Engineering (BSBE), Indian Institute of Technology Indore (IITI), Simrol, Indore, India.
Sajjan Rajpoot *Department of Biosciences and Biomedical Engineering (BSBE), Indian Institute of Technology Indore (IITI), Simrol, Indore, India.
Evgeny E BezsonovLaboratory of Cellular and Molecular Pathology of Cardiovascular System, Federal State Budgetary Scientific Institution "Petrovsky National Research Centre of Surgery", Moscow, Russia.
Alexander N OrekhovLaboratory of Cellular and Molecular Pathology of Cardiovascular System, Federal State Budgetary Scientific Institution "Petrovsky National Research Centre of Surgery", Moscow, Russia.
Rohit SalujaDepartment of Biochemistry, All India Institute of Medical Sciences, Bibinagar, Hyderabad, India.
Anita WaryPharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, United States.
Cassondra AxenPharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, United States.
Kishore WaryPharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, United States.
Mirza S BaigDepartment of Biosciences and Biomedical Engineering (BSBE), Indian Institute of Technology Indore (IITI), Simrol, Indore, India.
Indian Institute of Technology Indore · INUniversity of Illinois Chicago · USAll India Institute of Medical Sciences · INResearch Institute of General Pathology and Pathophysiology, the Russian Academy of Medical Sciences · RURussian Scientific Center of Surgery · RU

Funding

TRAINING PROGRAM IN LUNG BIOLOGY AND PATHOBIOLOGYT32HL007829 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DOLLY MEHTA · 1995 to 2026
$15.6M
Vascular Biology, Signaling and Therapeutics training programT32HL144459 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KITAJEWSKI, JAN K., WARY, KISHORE K · 2019 to 2023
$1.6M
NHLBI NIH HHS T32 HL007829NHLBI NIH HHS T32 HL144459
6 · The paper itself

Abstract

The nitric oxide synthases (NOS; EC 1.14.13.39) use L-arginine as a substrate to produce nitric oxide (NO) as a by-product in the tissue microenvironment. NOS1 represents the predominant NO-producing enzyme highly enriched in the brain and known to mediate multiple functions, ranging from learning and memory development to maintaining synaptic plasticity and neuronal development, Alzheimer's disease (AD), psychiatric disorders and behavioral deficits. However, accumulating evidence indicate both canonical and non-canonical roles of NOS1-derived NO in several other tissues and chronic diseases. A better understanding of NOS1-derived NO signaling, and identification and characterization of NO-metabolites in non-neuronal tissues could become useful in diagnosis and prognosis of diseases associated with NOS1 expression. Continued investigation on the roles of NOS1, therefore, will synthesize new knowledge and aid in the discovery of small molecules which could be used to titrate the activities of NOS1-derived NO signaling and NO-metabolites. Here, we address the significance of NOS1 and its byproduct NO in modifying pathophysiological events, which could be beneficial in understanding both the disease mechanisms and therapeutics.

Indexed as

Mental DisordersNitric OxideBrainHumansNitric Oxide SynthaseNitric Oxide Synthase Type INitric OxideNitric Oxide SynthaseNitric Oxide Synthase Type INOS1 protein, humanCancerCardiovascularDiabetesEpigeneticsNitric oxideNitric oxide signalingNitric oxide synthaseRedoxTranscriptional regulationVasodilation

Identifiers

PMID35821897
PMCPMC9271274
OpenAlexW4284672941

What Socratic 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 Socratic graph.