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DESCRIPTION (provided by applicant): Chronic pain is a global health care challenge and is poorly controlled by existing therapeutic strategies. This medical reality urges the development of safer and more effective analgesics. One approach is to identify novel analgesic targets. Our recent studies have suggested imidazoline I2 receptors as a novel drug target for acute nociception, although its role in chronic pain is less clear. As the etiology of many chronic pain conditions is multifaceted, combination therapy may be particularly effective against chronic pain by integrating multiple analgesic mechanisms of action. Although opioids are the most effective analgesics, their use is limited by concerns about abuse and the development of tolerance and dependence during chronic administration. Thus, combining opioids with other analgesics such as I2 receptor agonists may achieve better analgesic effects while decreasing some adverse effects of opioids. Building on exciting preliminary findings, studies described in this application will examine the antinociceptive and unwanted (tolerance and abuse liability) effects of I2 receptor agonists and test the feasibility of combining morphine and I2 receptor agonists against chronic pain. Mechanical and thermal hyperalgesia measures will be used to characterize the antinociceptive effects of I2 receptor agonists and morphine, alone or in combination, in models of complete Freund's adjuvant-induced inflammatory pain and chronic constriction injury-induced neuropathic pain (Aim I). Repeated treatment with I2 receptor agonists alone or combined with morphine will be performed to investigate the development of antinociceptive tolerance using the same procedures (Aim II). An intravenous self-administration procedure will be used to assess the reinforcing effects of I2 receptor agonists alone and how I2 receptor agonists modify the reinforcing effects of morphine (Aim III). Collectively, these experiments address two related and highly significant questions: (1) Do I2 receptor agonists represent a novel class of effective and safe analgesics for chronic pain and (2) Does the combination of I2 receptor agonists with morphine increase pain relief without increasing, or possibly decreasing, the abuse liability and development of tolerance.
期刊论文(35)
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会议论文
DOI: 10.1016/j.ejphar.2015.06.019
发表时间: 2015-08-15
期刊: European journal of pharmacology
影响因子: 5
作者: [Jing L, Li JX]
通讯作者: Li JX
Effects of imidazoline I2 receptor agonists on reserpine-induced hyperalgesia and depressive-like behavior in rats.
咪唑啉i2受体激动剂对复杂性诱导的痛觉过敏和大鼠抑郁样行为的影响。
DOI: 10.1097/fbp.0000000000000454
发表时间: 2019-08
期刊: Behavioural pharmacology
影响因子: 1.6
作者: [Siemian JN, Shang L, Seaman RW Jr, Zhu Q, Zhang Y, Li JX]
通讯作者: Li JX
Interactions between imidazoline I2 receptor ligands and acetaminophen in adult male rats: antinociception and schedule-controlled responding.
成年雄性大鼠中咪唑啉 I2 受体配体和对乙酰氨基酚之间的相互作用:镇痛和时间表控制反应。
DOI: 10.1007/s00213-015-4166-9
发表时间: 2016-03
期刊: Psychopharmacology
影响因子: 3.4
作者: [Siemian JN, Li J, Zhang Y, Li JX]
通讯作者: Li JX
DOI: 10.1016/j.ejphar.2013.03.002
发表时间: 2013-09-15
期刊: EUROPEAN JOURNAL OF PHARMACOLOGY
影响因子: 5
作者: [Li, Jun-Xu]
通讯作者: Li, Jun-Xu
19
    Development of LPA5 Antagonists as Analgesics
    • 批准号:
      10638278
    • 项目类别:
    • 资助金额:
      $188.17万
    • 财政年份:
      2023
    • 负责人:
      Jun-Xu Li
    • 依托单位:
    TAAR1 agonists for nicotine addiction
    TAAR1 agonists for nicotine addiction
    TAAR1 agonists for nicotine addiction
    海外基金