Evidence map›Paper›PMID 42378569›Full record

ArticleIndian journal of ophthalmology2026

Atropine reinstates inflammation-induced dysregulation of dopamine and its receptors in human scleral cells: Implications for myopia therapy.

Shivapriya Shivakumar, Nithin Kiran, Rohit Shetty, Pradhyumna Hulsermane Krishnamurthy, Arkasubhra Ghosh, Vrushali Deshpande, Nallathambi Jeyabalan

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Article in Indian journal of ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shivapriya ShivakumarGrow Research Laboratory, Narayana Netralaya Foundation, Bangalore, Karnataka.
Nithin KiranGrow Research Laboratory, Narayana Netralaya Foundation, Bangalore, Karnataka.
Rohit ShettyFaculty of Medicine and Life sciences, School of Mental Health and Neurosciences, Maastricht University, Maastricht, Netherlands.
Pradhyumna Hulsermane KrishnamurthyGrow Research Laboratory, Narayana Netralaya Foundation, Bangalore, Karnataka.
Arkasubhra GhoshGrow Research Laboratory, Narayana Netralaya Foundation, Bangalore, Karnataka.
Vrushali DeshpandeGrow Research Laboratory, Narayana Netralaya Foundation, Bangalore, Karnataka.
Nallathambi JeyabalanGrow Research Laboratory, Narayana Netralaya Foundation, Bangalore, Karnataka.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMyopia is a complex refractive disorder and a leading cause of visual impairment worldwide. Inflammation plays a crucial role in the onset and progression of myopia. This study aimed to investigate the role of atropine in modulating inflammation-induced alterations in dopamine and its receptors in primary human scleral cells under in vitro experimental conditions.

methodsHuman primary scleral cells were exposed to long-term inflammatory conditions in the presence or absence of atropine or dopamine hydrochloride. Following treatment, gene and protein expressions were analyzed for inflammatory markers, dopamine receptors, and extracellular matrix (ECM) using quantitative polymerase chain reaction, immunoblotting, and immunofluorescence. Secretory cytokines and dopamine levels were measured using an automated enzyme-linked immunosorbent assay system.

resultsIn primary human scleral cells, atropine treatment increases the dopamine receptor expression. Prolonged inflammatory stimulation led to a marked reduction in dopamine and its receptor (D1-D2) expression, which was effectively restored following atropine treatment in scleral cells. Under inflammatory conditions, atropine significantly suppressed pro-inflammatory cytokines expression at both the transcript and protein levels and mitigated the inflammation-induced dysregulation of ECM genes.

conclusionOur findings demonstrate atropine restores inflammation-induced dopaminergic and extracellular matrix dysregulation in human scleral cells, highlighting its dual anti-inflammatory and neuro-modulatory roles. The restoration of dopamine signaling and ECM balance underscores atropine's potential as a therapeutic agent for myopia.

Indexed as

AtropineDopamineGene Expression RegulationInflammationMyopiaReceptors, DopamineScleraCells, CulturedCytokinesEnzyme-Linked Immunosorbent AssayHumansMuscarinic AntagonistsAtropineCytokinesDopamineMuscarinic AntagonistsReceptors, DopamineAtropineDATdopaminedopamine receptorsinflammationmyopia

Identifiers

PMID42378569
PMCPMC13422903

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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.