Low dose systemic morphine attenuates operant escape but facilitates innate reflex responses to thermal stimulation

被引:45
作者
Vierck, CJ [1 ]
Acosta-Rua, A
Nelligan, R
Tester, N
Mauderli, A
机构
[1] Univ Florida, Coll Med, Dept Neurosci, McKnight Brain Inst, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Prosthodont, McKnight Brain Inst, Gainesville, FL 32610 USA
[3] Univ Florida, Coll Dent, Gainesville, FL 32610 USA
关键词
morphine; pain modulation; opioids; escape behavior;
D O I
10.1054/jpai.2002.125186
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Effects of systemic morphine on operant escape responses of rats to thermal stimulation were compared directly with effects on innate licking and guarding responses. For these independent tests, thermal stimulation was delivered via the floor of testing chambers with or without platforms that provided an escape option. The principal findings were (1) administration of 0.5 to 1.5 mg/kg morphine attenuated escape from nociceptive heat and (2) in distinct contrast, licking and guarding responses to heat were enhanced by these doses. When escape responding was calculated as time on the heated plate without licking or guarding, sensitivity to morphine was greater for 44degreesC than for 47degreesC or 50degreesC. Also, escape responses to cold (0degreesC or 10degreesC) were unaffected by 1.5 mg/kg morphine. The preferential reduction of heat nociception by morphine was demonstrated also by an operant preference task that gave the animals the option of standing on a cold (10degreesC) or a hot (45degreesC) surface. Administration of 0.5 mg/kg morphine increased occupancy of the hot surface. Platform time during operant tests was low and variable for warm stimulation (36degreesC) and was significantly increased by each level of heat, showing that platform occupancy represented escape from nociception rather than avoidance responses. A lack of significant effects of 1.5 mg/kg morphine on operant performance during cold or warm stimulation controls for effects of systemic morphine other than antinociception. (C) 2002 by the American Pain Society.
引用
收藏
页码:309 / 319
页数:11
相关论文
共 65 条
[1]  
Advokat C, 1999, EXP CLIN PSYCHOPHARM, V7, P219
[2]  
Bennett GJ, 2001, METH NE FRO NEUROSCI, P67
[3]   A PERIPHERAL MONONEUROPATHY IN RAT THAT PRODUCES DISORDERS OF PAIN SENSATION LIKE THOSE SEEN IN MAN [J].
BENNETT, GJ ;
XIE, YK .
PAIN, 1988, 33 (01) :87-107
[4]   PROGRESSIVE DEGRADATION OF SERIAL GROOMING CHAINS BY DESCENDING DECEREBRATION [J].
BERRIDGE, KC .
BEHAVIOURAL BRAIN RESEARCH, 1989, 33 (03) :241-253
[5]   ANALGESIC AND THERMAL RESPONSES TO INTRAVENOUSLY ADMINISTERED MORPHINE IN 8-WEEK-OLD AND 24-WEEK-OLD RATS [J].
BHARGAVA, HN ;
VILLAR, VM .
PHARMACOLOGY, 1991, 43 (05) :256-263
[6]   CHARACTERIZATION OF TAILSHOCK ELICITED WITHDRAWAL REFLEXES IN INTACT AND SPINAL RATS [J].
BORSZCZ, GS ;
JOHNSON, CP ;
ANDERSON, ME ;
YOUNG, BJ .
PHYSIOLOGY & BEHAVIOR, 1992, 52 (06) :1055-1062
[8]  
BORSZCZ GS, 1989, PHYSIOL BEHAV, V47, P101
[9]   EPIDURAL NARCOTICS IN VOLUNTEERS - SENSITIVITY TO PAIN AND TO CARBON-DIOXIDE [J].
BROMAGE, PR ;
CAMPORESI, E ;
LESLIE, J .
PAIN, 1980, 9 (02) :145-160
[10]  
CARROLL MN, 1960, ARCH INT PHARMACOD T, V125, P383