NITROUS OXIDE AND ENDOGENOUS OPIOID SYSTEMS
NITROUS OXIDE AND ENDOGENOUS OPIOID SYSTEMS
批准号:
2129410
负责人:
RAYMOND MARK QUOCK
金额:
$19.28万
依托单位国家:
美国
项目类别:
财政年份:
1984
资助国家:
美国
项目状态:
已结题
起止时间:
1984-12-01 至 1994-11-30
关键词:
analgesics blood chemistry blood pressure body temperature brain metabolism drug interactions drug tolerance endogenous opioid halothane high performance liquid chromatography laboratory rat microinjections narcotic antagonists neuropeptide receptor neuropharmacology nitrous oxide radioimmunoassay spinal cord stereotaxic techniques
中文摘要
一氧化二氮是一种气态药理学试剂,具有广泛的
医学和牙科的临床应用。 尽管使用
笑气作为临床镇痛剂的作用机制
仍然有些模糊。 我们实验室最近进行的研究
和其他地方暗示了亚麻醉浓度的相互作用
一氧化二氮与内源性阿片系统的结合 基于各种
实验结果,我们假设一氧化二氮镇痛可能
结果从药物刺激的神经元释放特定的内源性
阿片肽(EOPs),随后激活中枢神经系统
阿片受体介导的阿片受体。 在过去的几年里,
我们实验室的研究工作致力于进一步阐明,
在一氧化二氮镇痛作用中阿片类物质的这种联系。 的
本研究的目的是:(1)确定亚型(S)
以及介导一氧化二氮的中枢阿片受体的位置
镇痛;(2)量化和识别人工耳蜗中增加的EOP
从麻醉的和未麻醉的两个组织中收集脑脊液灌注液,
暴露于一氧化二氮的清醒、中枢灌注大鼠;和(3)
笑气镇痛的程度与区域性
脑和脊髓水平的EOP。 为了实现这一目标,双方
将采用生物和化学方法。 生物
方法将包括大鼠立体定位手术和内-
脑室/鞘内/脑内显微注射技术,
和镇痛试验(热板试验)。 化学方法将
包括心室-脑池/鞘内EOP放射免疫测定
灌流液和大鼠神经组织!暴露在一氧化二氮中,
EOP的高效液相色谱法(HPLC)分级
从暴露于一氧化二氮的大鼠的灌流液和组织样本中提取的。
要监测的其他参数包括吸入的麻醉剂、身体
体温、血压和血液化学。 的长期目标
这项持续的研究是系统地分析阿片类药物的性质,
一氧化二氮的药物作用和药效 的调查结果
这项研究应该增进我们对
一氧化二氮的药理学,这似乎是一个独特的和有用的
治疗和研究阿片类药物。 这项工作应有助于
更有效或明智的临床使用一氧化二氮,
医学和牙科。
英文摘要
Nitrous oxide is a gaseous pharmacological agent with a broad range of
clinical applications in medicine and dentistry. Despite the use of
nitrous oxide as a clinical analgesic agent, its mechanism of action
remains somewhat nebulous. Recent research conducted in our laboratory
and elsewhere implicates an interaction of subanesthetic concentrations
of nitrous oxide with endogenous opioid systems. Based on various
experimental findings, we hypothesize that nitrous oxide analgesia might
result from drug-stimulated neuronal release of specific endogenous
opioid peptides (EOPs) with subsequent activation of central
analgesia-mediating opioid receptors. Over the past several years,
research efforts in our laboratory have been devoted to further eluci-
dation of this opioid connection in nitrous oxide analgesia. The
objectives of this proposed research are to: (1) identify the subtype(s)
and location(s) of central opioid receptors that mediate nitrous oxide
analgesia; (2) quantify and identify the increased EOPs in artificial
cerebrospinal fluid perfusate collected from both anesthetized and
conscious, centrally perfused rats exposed to nitrous oxide; and (3)
correlate the degree of nitrous oxide analgesia with changes in regional
brain and spinal cord levels of EOPs. Towards these ends, both
biological and chemical approaches will be employed. The biological
approaches will include rat stereotaxic surgery and intra-
cerebroventricular/intrathecal/intracerebral microinjection technique,
and analgesia testing (hot plate test). The chemical approaches will
include radioimmunoassay for EOPs in ventricular-cisternal/intrathecal
perfusate and nervous tissues of rats !exposed to nitrous oxide, and
fractionation by high performance liquid chromatography (HPLC) for EOPs
from perfusate and tissue samples from rats exposed to nitrous oxide.
Other parameters to be monitored include inspired anesthetic agents, body
temperature, blood pressure and blood chemistry. The long term goal of
this continuing research is to systematically analyze the opioid nature
of the drug actions and drug effects of nitrous oxide. The findings of
this research should advance our understanding and knowledge of the
pharmacology of nitrous oxide, which appears to be a unique and useful
therapeutic and investigative opioid agent. This work should contribute
to more efficacious or judicious clinical use of nitrous oxide in
medicine and dentistry.
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Kinetic modeling of hormone release: application to time-averaged met-enkephalin release.
激素释放的动力学模型:应用于时间平均甲硫氨酸脑啡肽释放。
DOI:
10.1016/0306-4530(87)90066-7
发表时间:
1987
期刊:
Psychoneuroendocrinology
影响因子:
3.7
作者:
[Swartz,CM, Quock,RM]
通讯作者:
Quock,RM
Antagonism of nitrous oxide antinociception in the rat hot plate test by site-specific mu and epsilon opioid receptor blockade.
通过位点特异性 mu 和 epsilon 阿片受体阻断,在大鼠热板试验中拮抗一氧化二氮镇痛作用。
DOI:
--
发表时间:
1994
期刊:
The Journal of pharmacology and experimental therapeutics
影响因子:
--
作者:
[Hodges,BL, Gagnon,MJ, Gillespie,TR, Breneisen,JR, O'Leary,DF, Hara,S, Quock,RM]
通讯作者:
Quock,RM
Nitrous oxide-induced hypothermia in the rat.
一氧化二氮引起的大鼠体温过低。
DOI:
10.1016/0024-3205(87)90447-4
发表时间:
1987
期刊:
Life sciences
影响因子:
6.1
作者:
[Quock,RM, Panek,RW, Kouchich,FJ, Rosenthal,MA]
通讯作者:
Rosenthal,MA
Effect of subtype-selective opioid receptor blockers on nitrous oxide antinociception in rats.
亚型选择性阿片受体阻滞剂对大鼠笑气镇痛作用的影响。
DOI:
10.1016/1043-6618(90)90733-t
发表时间:
1990
期刊:
Pharmacological research
影响因子:
9.3
作者:
[Quock,RM, Walczak,CK, Henry,RJ, Chen,DC]
通讯作者:
Chen,DC
Interaction between Nitrous Oxide and Diazepam in the Mouse Staircase Test
小鼠阶梯试验中一氧化二氮和地西泮的相互作用
DOI:
--
发表时间:
1989
期刊:
Anesthesia and Analgesia
影响因子:
5.7
作者:
[R. J. Pruhs, R. Quock]
通讯作者:
R. Quock
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GENETIC CONTROL OF RESPONSIVENESS TO N20 ANTIOCICEPTION
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GENETIC CONTROL OF RESPONSIVENESS TO N20 ANTIOCICEPTION
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资助金额:$7.71万
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资助金额:$9.08万
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依托单位:
NITROUS OXIDE CONSCIOUS SEDATION--ANXIOYSIS
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项目类别:
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资助金额:$6.05万
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资助金额:$23.26万
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项目类别:
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资助金额:$20.78万
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海外基金