Literature DB >> 31096011

Redox TRPs in diabetes and diabetic complications: Mechanisms and pharmacological modulation.

Pratik Adhya1, Shyam Sunder Sharma2.   

Abstract

Transient receptor potential (TRP) channels have shown to be involved in a wide variety of physiological functions and pathophysiological conditions. Modulation of TRP channels reported to play a major role in number of disorders starting from central nervous system related disorders to cardiovascular, inflammatory, cancer, gastrointestinal and metabolic diseases. Recently, a subset of TRP ion channels called redox TRPs gained importance on account of their ability to sense the cellular redox environment and respond accordingly to such redox stimuli. Diabetes, the silent epidemic of the world is increasing at an alarming rate in spite of novel therapeutic interventions. Moreover, diabetes and its associated complications are reported to arise due to a change in oxidative status of cell induced by hyperglycemia. Such a change in cellular oxidative status can modulate the activities of various redox TRP channels (TRPA1, TRPC5, TRPMs and TRPV1). Targeting redox TRPs have potential in diabetes and diabetic complications like neuropathy, cardiomyopathy, retinopathy, cystopathy, and encephalopathy. Thus in this review, we have discussed the activities of different redox sensing TRPs in diabetes and diabetic complications and how they can be modulated pharmacologically, so as to consider them a potential novel therapeutic target in treating diabetes and its comorbidity.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  2-aminoethoxydiphenyl borate (PubMed CID: 1598); Adenosine diphosphate ribose (PubMed CID: 30243); Allyl isothiocyanate (PubMed CID: 5971); Capsaicin (PubMed CID: 1548943); Capsazepine (PubMed CID: 2733484); Diabetes; Diabetic complications; HC030031 (PubMed CID: 5754); ML204 (PubMed CID: 230710); N-(p-amylcinnamoyl) anthranilic acid (PubMed CID: 5353376); Oxidative stress; Redox TRP channels; Resiniferatoxin (PubMed CID: 68029831); TRP channels; Waixenicin A (PubMed CID: 73755210).

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Year:  2019        PMID: 31096011     DOI: 10.1016/j.phrs.2019.104271

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  8 in total

1.  Neuroprotective Effect of 2-Aminoethoxydiphenyl Borate (2-APB) in Amyloid β-Induced Memory Dysfunction: A Mechanistic Study.

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2.  Pharmacological Modulation of TRPM2 Channels via PARP Pathway Leads to Neuroprotection in MPTP-induced Parkinson's Disease in Sprague Dawley Rats.

Authors:  Bhupesh Vaidya; Harpinder Kaur; Pavan Thapak; Shyam Sunder Sharma; Jitendra Narain Singh
Journal:  Mol Neurobiol       Date:  2022-01-08       Impact factor: 5.590

3.  Kunitz-Type Peptides from Sea Anemones Protect Neuronal Cells against Parkinson's Disease Inductors via Inhibition of ROS Production and ATP-Induced P2X7 Receptor Activation.

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Journal:  Int J Mol Sci       Date:  2022-05-04       Impact factor: 6.208

4.  Therapeutic effects of SKF-96365 on murine allergic rhinitis induced by OVA.

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Journal:  Int J Immunopathol Pharmacol       Date:  2021 Jan-Dec       Impact factor: 3.219

Review 5.  Cutaneous pain in disorders affecting peripheral nerves.

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Journal:  Neurosci Lett       Date:  2021-10-01       Impact factor: 3.046

6.  Effects of Dexmedetomidine on the RhoA /ROCK/ Nox4 Signaling Pathway in Renal Fibrosis of Diabetic Rats.

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Journal:  Open Med (Wars)       Date:  2019-11-20

Review 7.  Transient Receptor Potential Channels as an Emerging Target for the Treatment of Parkinson's Disease: An Insight Into Role of Pharmacological Interventions.

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Journal:  Front Cell Dev Biol       Date:  2020-11-20

8.  Tranilast, a Transient Receptor Potential Vanilloid 2 Channel (TRPV2) Inhibitor Attenuates Amyloid β-Induced Cognitive Impairment: Possible Mechanisms.

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Journal:  Neuromolecular Med       Date:  2021-07-06       Impact factor: 3.843

  8 in total

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