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首页> 外文期刊>American Journal of Physiology >Assessment of heat production, heat loss, and core temperature during nitrous oxide exposure: a new paradigm for studying drug effects and opponent responses.
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Assessment of heat production, heat loss, and core temperature during nitrous oxide exposure: a new paradigm for studying drug effects and opponent responses.

机译:评估暴露于一氧化二氮期间的热量产生,热量损失和核心温度:研究药物作用和对手反应的新范例。

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Studies using core temperature (T(c)) have contributed greatly to theoretical explanations of drug tolerance and its relationship to key features of addiction, including dependence, withdrawal, and relapse. Many theoretical accounts of tolerance propose that a given drug-induced psychobiological disturbance elicits opponent responses that contribute to tolerance development. This proposal and its theoretical extensions (e.g., conditioning as a mechanism of chronic tolerance) have been inferred from dependent variables, such as T(c), which represent the summation of multiple underlying determinants. Direct measurements of determinants could increase the understanding of opponent processes in tolerance, dependence, and withdrawal. The proximal determinants of T(c) are metabolic heat production (HP) and heat loss (HL). We developed a novel system for simultaneously quantifying HP (indirect calorimetry), HL (direct gradient layer calorimetry), and T(c) (telemetry) during steady-state administrations of nitrous oxide (N(2)O), an inhalant with abuse potential that has been previously used to study acute and chronic tolerance development to its hypothermia-inducing property. Rats were administered 60% N(2)O (n = 18) or placebo gas (n = 16) for 5 h after a 2-h placebo baseline exposure. On average, N(2)O rapidly but transiently lowered HP and increased HL, each by approximately 16% (P < 0.001). On average, rats reestablished and maintained thermal equilibrium (HP = HL) at a hypothermic T(c) (-1.6 degrees C). However, some rats entered positive heat balance (HP > HL) after becoming hypothermic such that acute tolerance developed, i.e., T(c) rose despite continued drug administration. This work is the first to directly quantify the thermal determinants of T(c) during administration of a drug of abuse and establishes a new paradigm for studying opponent processes involved in acute and chronic hypothermic tolerance development.
机译:使用核心温度(T(c))的研究为药物耐受性及其与成瘾关键特征(包括依赖性,戒断和复发)之间关系的理论解释做出了巨大贡献。宽容的许多理论说明表明,给定的药物诱发的心理生物学障碍会引起有助于宽容发展的对手反应。该提议及其理论扩展(例如,条件调节作为慢性耐受的机制)已从诸如T(c)的因变量中推断出来,这些因变量表示多个潜在决定因素的总和。直接测量行列式可以增加对对手过程在宽容,依赖性和退缩方面的理解。 T(c)的近端决定因素是代谢热产生(HP)和热损失(HL)。我们开发了一种新型系统,用于在稳态滥用一氧化二氮(N(2)O)稳态给药期间同时定量HP(间接量热法),HL(直接梯度层量热法)和T(c)(遥测法)以前已被用于研究其诱导低温的急性和慢性耐受性发展的潜力。安慰剂基线暴露2小时后,大鼠接受60%N(2)O(n = 18)或安慰剂气体(n = 16)施用5 h。平均而言,N(2)O迅速但短暂地降低了HP,并增加了HL,两者分别降低了约16%(P <0.001)。平均而言,大鼠在体温较低的T(c)(-1.6摄氏度)下恢复并维持了热平衡(HP = HL)。但是,一些大鼠在变为低温后进入正热平衡(HP> HL),从而尽管继续给药,急性耐受性也有所提高,即T(c)升高。这项工作是第一个在滥用药物管理期间直接量化T(c)的热决定因素的方法,并为研究参与急性和慢性低温耐受性发展的对手过程建立了新的范例。

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