The TWIK-related K+ channel, TREK-1, has recently emerged as an attractive therapeutic target for the development of a novel class of analgesic drugs, suggesting that activation of TREK-1 could result in pain inhibition. Here, we report the synthesis of a series of substituted acrylic acids (1-54) based on our previous work with caffeate...
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February 9, 2017 (v1)Journal articleUploaded on: December 4, 2022
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May 19, 2015 (v1)Journal article
Cold-triggered pain is essential to avoid prolonged exposure to harmfully low temperatures. However, the molecular basis of noxious cold sensing in mammals is still not completely understood. Here, we show that the voltage-gated Nav1.9 sodium channel is important for the perception of pain in response to noxious cold. Nav1.9 activity is...
Uploaded on: March 26, 2023 -
May 2015 (v1)Journal article
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Uploaded on: December 8, 2023 -
May 2015 (v1)Journal article
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Uploaded on: December 8, 2023 -
September 21, 2020 (v1)Journal article
Background and Purpose: Opioids are effective painkillers. However, their risk-benefit ratio is dampened by numerous adverse effects and opioid misuse has led to a public health crisis. Safer alternatives are required, but isolating the antinociceptive effect of opioids from their adverse effects is a pharmacological challenge because...
Uploaded on: December 3, 2022 -
September 21, 2020 (v1)Journal article
Background and Purpose Opioids are effective painkillers. However, their risk–benefit ratio is dampened by numerous adverse effects and opioid misuse has led to a public health crisis. Safer alternatives are required, but isolating the antinociceptive effect of opioids from their adverse effects is a pharmacological challenge because activation...
Uploaded on: December 8, 2023