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The effects of nalbuphine and fentanyl on experimental spinal cord injuries

Lee WH

Opiate receptor agonists (especially dynorphin - a kappa receptor agonist) have found to increase in the injuried segment of spinal cord. It is known to cause spinal cord damage when...
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Mu-Opioid Receptor Polymorphisms and Breast Cancer in a Korean Female Adult Population: A Retrospective Study

Oh CS, Lee SH, Yoo YB, Yang JH, Kim SH

Distribution of A118G single nucleotide polymorphism (SNP) in the mu-opioid receptor 1 gene (OPRM1) differs with ethnicity. We assessed the distribution of this SNP in Korean women with breast cancer...
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Can oliceridine (TRV130), an ideal novel µ receptor G protein pathway selective (µ-GPS) modulator, provide analgesia without opioid-related adverse reactions?

Ok HG, Kim SY, Lee SJ, Kim TK, Huh BK, Kim KH

All drugs have both favorable therapeutic and untoward adverse effects. Conventional opioid analgesics possess both analgesia and adverse reactions, such as nausea, vomiting, and respiratory depression. The opioid ligand binds...
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The Effects of Peripheral mu and kappa Opioid Receptor Agonists on the Thermal Injury Induced Hyperalgesia in the Rat

Chun YS, Jun JH, Shim JC, Kim KS, Suh JK, Yoo HK, Seung IS

BACKGROUND: Previous reports have described that the local administration of opioid receptor agonist can attenuate the nociceptive responses induced by a variety of inflammatory states. This study evaluated the effects...
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Comparison of Blood Pressure and Heart Rate in Pediatric Tonsillectomy under Propofol-Remifentanil Anesthesia and Desflurane-N2O Anesthesia

Lee DH, Kim DY, Park SW, Shin OY

  • KMID: 1917406
  • Anesth Pain Med.
  • 2007 Apr;2(2):74-77.
BACKGROUND: Remifentanil is an ultra-short-acting mu opioid receptor agonist. However, there are few reports of its use in children. Therefore, this study compared propofol-remifentanil anesthesia (PR) with a desflurane-N2O anesthesia...
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The Effect of Morphine on REST Expression in Human Neuroblastoma NMB Cells

Kim DK, Kim CS, Kim HJ, Kook JK, Kim SH, Lee BH, Lee YH, Mo SY, Loh HH

  • KMID: 1457120
  • Int J Oral Biol.
  • 2010 Jun;35(2):69-74.
The mu opioid receptor (MOR) has been regarded as the main site of interaction with analgesics in major clinical use, particularly morphine. The repressor element-1 silencing transcription factor (REST) functions...
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Tapentadol: Can It Kill Two Birds with One Stone without Breaking Windows?

Chang EJ, Choi EJ, Kim KH

Tapentadol is a novel oral analgesic with a dual mode of action as an agonist of the µ-opioid receptor (MOR), and as a norepinephrine reuptake inhibitor (NRI) all in a...
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Effects of micro-Opioid Receptor Gene Polymorphism on Postoperative Nausea and Vomiting in Patients Undergoing General Anesthesia with Remifentanil: Double Blinded Randomized Trial

Lee SH, Kim JD, Park SA, Oh CS, Kim SH

Association between postoperative nausea and vomiting (PONV) and micro-opioid receptor A118G single nucleotide polymorphism (SNP) is undefined and might underlie inconsistent results of studies on PONV occurrence in patients undergoing...
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The Effect of Mu Agonist on Seizure in Hippocampus

Choi BJ, Kim JS

  • KMID: 2007316
  • J Korean Child Neurol Soc.
  • 2001 Oct;9(2):289-296.
PURPOSE: Mu agonists can be used in clinical conditions where threr is a risk of hypoxic neurosusceptibility. Fentanyl, one of mu agonists may serve as neuroprotection from brain ischemic injury...
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Pharmacotherapy for Alcohol Dependence: Anticraving Medications for Relapse Prevention

Jung YC, Namkoong K

Alcohol dependence is a chronic disorder that results from a variety of genetic, psychosocial, and environmental factors. Relapse prevention for alcohol dependence has traditionally involved psychosocial and psychotherapeutic interventions. Pharmacotherapy,...
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The Analgesic Interactions Among Intrathecal Morphine, Ketorolac and L-NAME on Formalin-induced Pain in Rats

Shim JH, Jun JH, Kim KH, Yeom JH, Suh JK

BACKGROUND: Morphine has a direct action on morphine receptors in the brain and spinal cord. Intrathecally administered L-NAME, a nitric oxide synthase inhibitor, is known to have an antinociceptive effect...
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Effect of Intraperitoneal Nalbuphine-HCl on C-fos Expression in Rat Brain induced by Incisional Pain

Park CS, Park CM, Joong JY

BACKGROUND: Nalbuphine-HCl (Nubain(R)), an agonist-antagonist of kappa3 and mu receptors, has limited analgesic or sedative effects, and an effect ceiling. It is generally accepted that c-fos is a marker of...
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