Evidence map›Paper›PMID 40092747›Full record

ArticleAnnals of neurosciences2025

Amelioration of Glutamate-induced Toxicity by a New Thyrotropin-releasing Hormone (TRH) Analogue PYR-l-(2,5-Dibromo)-His-l-ProNH

Mallikarjuna R Sunkara, Jitendra N Singh, C L Meena, A B Pant, Rahul Jain, Shyam S Sharma

Abstract read
In one paragraph

Article in Annals of neurosciences, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mallikarjuna R SunkaraDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Mohali, Punjab, India.
Jitendra N SinghDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Mohali, Punjab, India.ORCID https://orcid.org/0000-0003-0045-9295
C L MeenaDepartment of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research, Mohali, Punjab, India.
A B PantIndian Institute of Toxicology Research, Lucknow, Uttar Pradesh, India.
Rahul JainDepartment of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research, Mohali, Punjab, India.
Shyam S SharmaDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Mohali, Punjab, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Glutamate has been implicated in the pathophysiology of central nervous system diseases, including stroke. Purpose: In this study, the neuroprotective potential of the newly synthesised thyrotropin-releasing hormone (TRH) analogue [Pyr-l-(2,5-dibromo)-His-l-ProNH Methods: Cortical neurons isolated from neonatal rats were used to evaluate the effects of the NP-2376. Cortical neurons were pre-treated with NP-2376 (6, 12 and 24 h) prior to glutamate (15 mM) exposure. Cell viability was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and neutral red uptake (NRU) assay, and oxidative stress by chloromethyl-2,7-dichlorodihydrofluorescein diacetate (DCFH-DA) and glutathione assays. Results: NP-2376 protected against glutamate-induced cortical neuron death and oxidative stress in a dose-dependent manner. Conclusions: This study demonstrates the neuroprotective potential of TRH analogue NP-2376 against glutamate-induced toxicity, which is attributed to a decrease in oxidative stress.

Indexed as

3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromidechloromethyl-2,7-dichlorodihydrofluorescein diacetatecortical neuronglutamateglutathioneneutral red uptakePyr-l-(2,5-dibromo)-His-l-ProNH2thyrotropin-releasing hormone

Identifiers

PMID40092747
PMCPMC11907565

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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.