Literature DB >> 15563578

Assessment of heat production, heat loss, and core temperature during nitrous oxide exposure: a new paradigm for studying drug effects and opponent responses.

Karl J Kaiyala1, Douglas S Ramsay.   

Abstract

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.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15563578     DOI: 10.1152/ajpregu.00412.2004

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  14 in total

1.  Nitrous oxide causes a regulated hypothermia: rats select a cooler ambient temperature while becoming hypothermic.

Authors:  Douglas S Ramsay; Jana Seaman; Karl J Kaiyala
Journal:  Physiol Behav       Date:  2010-12-22

2.  Clarifying the roles of homeostasis and allostasis in physiological regulation.

Authors:  Douglas S Ramsay; Stephen C Woods
Journal:  Psychol Rev       Date:  2014-04       Impact factor: 8.934

3.  Systems-level adaptations explain chronic tolerance development to nitrous oxide hypothermia in young and mature rats.

Authors:  Karl J Kaiyala; Shehzad Butt; Douglas S Ramsay
Journal:  Psychopharmacology (Berl)       Date:  2007-01-10       Impact factor: 4.530

4.  Robust thermoregulatory overcompensation, rather than tolerance, develops with serial administrations of 70% nitrous oxide to rats.

Authors:  Karl J Kaiyala; Ben Chan; Douglas S Ramsay
Journal:  J Therm Biol       Date:  2012-01-01       Impact factor: 2.902

5.  Individual differences in initial sensitivity and acute tolerance predict patterns of chronic drug tolerance to nitrous-oxide-induced hypothermia in rats.

Authors:  Douglas S Ramsay; Karl J Kaiyala; Brian G Leroux; Stephen C Woods
Journal:  Psychopharmacology (Berl)       Date:  2005-10-15       Impact factor: 4.530

Review 6.  Direct animal calorimetry, the underused gold standard for quantifying the fire of life.

Authors:  Karl J Kaiyala; Douglas S Ramsay
Journal:  Comp Biochem Physiol A Mol Integr Physiol       Date:  2010-04-25       Impact factor: 2.320

Review 7.  Food intake, metabolism and homeostasis.

Authors:  Stephen C Woods; Douglas S Ramsay
Journal:  Physiol Behav       Date:  2011-04-28

8.  Direct evidence for systems-level modulation of initial drug (in)sensitivity in rats.

Authors:  Karl J Kaiyala; Shezhad Butt; Douglas S Ramsay
Journal:  Psychopharmacology (Berl)       Date:  2007-01-20       Impact factor: 4.530

9.  Brown adipose tissue thermogenesis does not explain the intra-administration hyperthermic sign-reversal induced by serial administrations of 60% nitrous oxide to rats.

Authors:  Salwa Al-Noori; Douglas S Ramsay; Andreas Cimpan; Zoe Maltzer; Jessie Zou; Karl J Kaiyala
Journal:  J Therm Biol       Date:  2016-07-20       Impact factor: 2.902

10.  Repeated nitrous oxide exposure in rats causes a thermoregulatory sign-reversal with concurrent activation of opposing thermoregulatory effectors.

Authors:  Douglas S Ramsay; Stephen C Woods; Karl J Kaiyala
Journal:  Temperature (Austin)       Date:  2014 Oct-Dec
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.