Literature DB >> 30325008

Two-pore domain potassium channels: emerging targets for novel analgesic drugs: IUPHAR Review 26.

Kirin Gada1, Leigh D Plant1.   

Abstract

Chronic pain is a debilitating and increasingly common medical problem with few effective treatments. In addition to the direct and indirect economic burden of pain syndromes, the concomitant increase in prescriptions for narcotics has contributed to a sharp rise in deaths associated with drug misuse - the 'opioid crisis'. Together, these issues highlight the unmet clinical and social need for a new generation of safe, efficacious analgesics. The detection and transmission of pain stimuli is largely mediated by somatosensory afferent fibres of the dorsal root ganglia. These nociceptive cells express an array of membrane proteins that have received significant attention as attractive targets for new pain medications. Among these, a growing body of evidence supports a role for the two-pore domain potassium (K2P) family of K+ channels. Here, we provide a concise review of the K2P channels, their role in pain biology and their potential as targets for novel analgesic agents.
© 2018 The British Pharmacological Society.

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Year:  2018        PMID: 30325008      PMCID: PMC6295411          DOI: 10.1111/bph.14518

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  92 in total

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Review 3.  TRP channels and pain.

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5.  Reduction of breast cancer cell migration via up-regulation of TASK-3 two-pore domain K+ channel.

Authors:  G-W Lee; H S Park; E-J Kim; Y-W Cho; G-T Kim; Y-J Mun; E-J Choi; J-S Lee; J Han; D Kang
Journal:  Acta Physiol (Oxf)       Date:  2011-10-07       Impact factor: 6.311

6.  Reversal of TRESK Downregulation Alleviates Neuropathic Pain by Inhibiting Activation of Gliocytes in the Spinal Cord.

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Journal:  Neurochem Res       Date:  2017-02-03       Impact factor: 3.996

7.  TREK-1, a K+ channel involved in polymodal pain perception.

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8.  Inhibition of a background potassium channel by Gq protein alpha-subunits.

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9.  TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure.

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  19 in total

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2.  Kv4.3 Channel Dysfunction Contributes to Trigeminal Neuropathic Pain Manifested with Orofacial Cold Hypersensitivity in Rats.

Authors:  Hirosato Kanda; Jennifer Ling; Ya-Ting Chang; Ferhat Erol; Viacheslav Viatchenko-Karpinski; Akihiro Yamada; Koichi Noguchi; Jianguo G Gu
Journal:  J Neurosci       Date:  2021-01-20       Impact factor: 6.167

3.  The Polysite Pharmacology of TREK K2P Channels.

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Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

Review 4.  Ion channel long non-coding RNAs in neuropathic pain.

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Review 5.  Molecular dynamics: a powerful tool for studying the medicinal chemistry of ion channel modulators.

Authors:  Daniel Şterbuleac
Journal:  RSC Med Chem       Date:  2021-07-22

Review 6.  Two-Pore Domain Potassium Channel in Neurological Disorders.

Authors:  Punita Aggarwal; Sanjiv Singh; V Ravichandiran
Journal:  J Membr Biol       Date:  2021-06-24       Impact factor: 1.843

7.  Comparison of K+ Channel Families.

Authors:  Jaume Taura; Daniel M Kircher; Isabel Gameiro-Ros; Paul A Slesinger
Journal:  Handb Exp Pharmacol       Date:  2021

8.  Pharmacologically reversible, loss of function mutations in the TM2 and TM4 inner pore helices of TREK-1 K2P channels.

Authors:  Ehab Al-Moubarak; Emma L Veale; Alistair Mathie
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9.  Block of TREK and TRESK K2P channels by lamotrigine and two derivatives sipatrigine and CEN-092.

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