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Opioid Modulation of Immunocompetence

Opioid Modulation of Immunocompetence
阿片类药物对免疫能力的调节
批准号:
6603907
负责人:
JEAN M BIDLACK
金额:
$27.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-08-01 至 2006-06-30

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DESCRIPTION: (provided by applicant) This competitive renewal proposal is directed at determining which cells from the mouse immune system express 6, g and K opioid receptors, and whether activation of these cells alters the amount of receptor expressed and the distribution of the multiple opioid receptors among the different lymphocyte populations. By using fluorescent opioids and flow cytometry, we have developed a novel indirect fluorescent method for detecting about: opioid receptors. This method is more sensitive than radioreceptor binding methodology. Double-labeling experiments have shown the highest level of about receptor expression on mouse thymocytes and macrophages, and on human microglial cells. The studies proposed in this application focus on the detection of 6 and/.t opioid receptors. Based on functional studies, the first hypothesis to be tested is that mouse thymocytes and CD4+ and CD8+ T cells express ;5 opioid receptors. To detect 6 receptors, two approaches will be compared. FITC-labeled derivatives of the 6-selective ligand, naltrindole, will be used in a manner similar to the labeling of the receptor with the FITC-conjugated K ligand. The second approach will use specific antibodies directed against the 6 receptor. The second hypothesis to be tested is that mouse peritoneal and T cells express the/,t opioid receptor. The g receptor will be labeled with either a FITC-labeled derivative of fentanyl or morphine, and/or antibodies directed against the la opioid receptor. Flow cytometry will be used to detect the labeled receptors. For both 6 and g receptors, the goal is to develop an optimal method for detecting the receptor, and then to use this method to study receptor expression. The third hypothesis is that activation of lymphocytes will increase the expression of opioid receptors since levels of receptor mRNA have been shown to increase with cell activation. Collectively, these studies will use an innovative approach and technique to determine which cells from the immune express about:, 6, and about opioid receptors and if receptor expression is altered with activation of the cells. These studies will lay the foundation for determining the cellular mechanisms by which opioids alter immune function and immunological responses to viral infection, including AIDS.
期刊论文(23)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1016/0006-2952(94)00440-w
发表时间: 1995-01
期刊: Biochemical pharmacology
影响因子: 5.8
作者: [D. M. Lawrence;D. Joseph;J. Bidlack]
通讯作者: D. M. Lawrence;D. Joseph;J. Bidlack
Changes in kappa opioid receptor expression during maturation of mouse lymphocytes.
小鼠淋巴细胞成熟过程中 kappa 阿片受体表达的变化。
DOI: 10.1007/978-1-4615-5347-2_13
发表时间: 1998
期刊: Advances in experimental medicine and biology
影响因子: --
作者: [Ignatowski,TA, Bidlack,JM]
通讯作者: Bidlack,JM
Kappa-opioid receptor agonist suppression of HIV-1 expression in CD4+ lymphocytes.
Kappa-阿片受体激动剂抑制 CD4 淋巴细胞中 HIV-1 的表达。
DOI: 10.1016/s0006-2952(01)00574-3
发表时间: 2001
期刊: Biochemical pharmacology
影响因子: 5.8
作者: [Peterson,PK, Gekker,G, Lokensgard,JR, Bidlack,JM, Chang,AC, Fang,X, Portoghese,PS]
通讯作者: Portoghese,PS
Kappa opioid binding sites on the R1.1 murine lymphoma cell line: sensitivity to cations and guanine nucleotides.
R1.1 鼠淋巴瘤细胞系上的 Kappa 阿片类药物结合位点:对阳离子和鸟嘌呤核苷酸的敏感性。
DOI: 10.1016/0165-5728(92)90073-t
发表时间: 1992
期刊: Journal of neuroimmunology
影响因子: 3.3
作者: [Lawrence,DM, Bidlack,JM]
通讯作者: Bidlack,JM
17
    G alpha Z subunit as a potential therapeutic target to modulate mu opioid receptor pharmacology
    • 批准号:
      10580415
    • 项目类别:
    • 资助金额:
      $42.35万
    • 财政年份:
      2022
    • 负责人:
      JEAN M BIDLACK
    • 依托单位:
    38th Annual International Narcotics Research Conference
    37th Annual International Narcotics Research Conference
    36th Annual International Narcotics Research Conference
    海外基金