Literature DB >> 15778887

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

Douglas S Ramsay1, Karl J Kaiyala, Brian G Leroux, Stephen C Woods.   

Abstract

RATIONALE: A preventive strategy for drug addiction would benefit from being able to identify vulnerable individuals. Understanding how an individual responds during an initial drug exposure may be useful for predicting how that individual will respond to repeated drug administrations.
OBJECTIVES: This study investigated whether individual differences in initial drug sensitivity and acute tolerance can predict how chronic tolerance develops.
METHODS: During an initial 3-h administration of 60% nitrous oxide (N(2)O), male Long-Evans rats were screened for N(2)O's hypothermic effect into subsets based on being initially insensitive (II), sensitive with acute tolerance (AT), or sensitive with no intrasessional recovery (NR). Animals in each individual difference category were randomly assigned to receive six 90-min exposures of either 60% N(2)O or placebo gas. Core temperature was measured telemetrically.
RESULTS: Rats that exhibited a comparable degree of hypothermia during an initial N(2)O exposure, but differed in acute tolerance development, developed different patterns of chronic tolerance. Specifically, the NR group did not become fully tolerant over repeated N(2)O exposures while the AT group developed an initial hyperthermia followed by a return of core temperature to control levels indicative of full tolerance development. By the second N(2)O exposure, the II group breathing N(2)O became hyperthermic relative to the placebo control group and this hyperthermia persisted throughout the multiple N(2)O exposures.
CONCLUSIONS: Individual differences in initial drug sensitivity and acute tolerance development predict different patterns of chronic tolerance. The hypothesis is suggested that individual differences in opponent-adaptive responses may mediate this relationship.

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Year:  2005        PMID: 15778887      PMCID: PMC1470882          DOI: 10.1007/s00213-005-2219-1

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  63 in total

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3.  Phenotypic and genotypic relationships between ethanol tolerance and sensitivity in mice selectively bred for initial sensitivity to ethanol (SS and LS) or development of acute tolerance (HAFT and LAFT).

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Authors:  L Tampier; M E Quintanilla; J Mardones
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5.  The genetics of acute functional tolerance and initial sensitivity to ethanol for an ataxia test in the LSxSS RI strains.

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Review 6.  The therapeutic potential of regulated hypothermia.

Authors:  C J Gordon
Journal:  Emerg Med J       Date:  2001-03       Impact factor: 2.740

7.  Sensitivity and tolerance to ethanol in mouse lines selected for ethanol-induced hypothermia.

Authors:  K E Browman; N R Rustay; N Nikolaidis; L Crawshaw; J C Crabbe
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8.  Genetic differences in alcohol sensitivity and the inheritance of alcoholism risk.

Authors:  A C Heath; P A Madden; K K Bucholz; S H Dinwiddie; W S Slutske; L J Bierut; J W Rohrbaugh; D J Statham; M P Dunne; J B Whitfield; N G Martin
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9.  A genome-wide search for genes that relate to a low level of response to alcohol.

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10.  Induction of steady-state blood alcohol levels: application to the study of within-session alcohol tolerance in rats.

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  13 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

Review 5.  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

6.  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

7.  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

8.  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

9.  Predicting addictive vulnerability: individual differences in initial responding to a drug's pharmacological effects.

Authors:  Douglas S Ramsay; Salwa Al-Noori; Jason Shao; Brian G Leroux; Stephen C Woods; Karl J Kaiyala
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10.  Drug-induced regulatory overcompensation has motivational consequences: Implications for homeostatic and allostatic models of drug addiction.

Authors:  Douglas S Ramsay; Stephen C Woods; Karl J Kaiyala
Journal:  Temperature (Austin)       Date:  2014
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