TY - JOUR
T1 - Gender differences in the reinforcing properties of morphine
AU - Cicero, Theodore J.
AU - Ennis, Terri
AU - Ogden, Justin
AU - Meyer, Edward R.
N1 - Funding Information:
This research was supported in part by USPHS Grants DA03833 (T.J.C.), DA09140 (T.J.C.), and DA09344 (B.N.) from the National Institute on Drug Abuse.
PY - 2000/1
Y1 - 2000/1
N2 - The purpose of the present studies was to examine whether gender differences could be observed in an important aspect of morphine’s pharmacology: its reinforcing properties. Our results showed that morphine served as a positive reinforcing agent in both male and female rats in a place conditioning paradigm, but that the dose-response curves displayed marked sex-related differences. At doses from 0.2 up to 10.0 mg/kg, morphine induced an equally strong preference for the drug-associated chamber in males and females. However, as the dose was increased from 10-17.5 mg/kg, morphine ceased to act as a positive reinforcer in males. In contrast, a very strong preference for the morphine-associated chamber was still observed in females at doses up to 30 mg/kg. No gender differences in the blood and brain levels of morphine were observed subsequent to morphine administration during the conditioning phase, suggesting that pharmacokinetic factors were not involved in the sex-related differences observed. Consequently, these results suggest that there are intrinsic sex-linked differences in the doses of morphine that can induce a preference for the drug-associated chamber in a place- conditioning paradigm that are most likely related to differences in the sensitivity of the central nervous system to morphine’s reinforcing properties in males and females.
AB - The purpose of the present studies was to examine whether gender differences could be observed in an important aspect of morphine’s pharmacology: its reinforcing properties. Our results showed that morphine served as a positive reinforcing agent in both male and female rats in a place conditioning paradigm, but that the dose-response curves displayed marked sex-related differences. At doses from 0.2 up to 10.0 mg/kg, morphine induced an equally strong preference for the drug-associated chamber in males and females. However, as the dose was increased from 10-17.5 mg/kg, morphine ceased to act as a positive reinforcer in males. In contrast, a very strong preference for the morphine-associated chamber was still observed in females at doses up to 30 mg/kg. No gender differences in the blood and brain levels of morphine were observed subsequent to morphine administration during the conditioning phase, suggesting that pharmacokinetic factors were not involved in the sex-related differences observed. Consequently, these results suggest that there are intrinsic sex-linked differences in the doses of morphine that can induce a preference for the drug-associated chamber in a place- conditioning paradigm that are most likely related to differences in the sensitivity of the central nervous system to morphine’s reinforcing properties in males and females.
KW - Gender differences
KW - Morphine, gender differences
KW - Morphine, reinforcing properties
KW - Opiates, gender differences
KW - Opiates, reinforcing properties
UR - http://www.scopus.com/inward/record.url?scp=0033985822&partnerID=8YFLogxK
U2 - 10.1016/S0091-3057(99)00174-4
DO - 10.1016/S0091-3057(99)00174-4
M3 - Article
C2 - 10638641
AN - SCOPUS:0033985822
SN - 0091-3057
VL - 65
SP - 91
EP - 96
JO - Pharmacology Biochemistry and Behavior
JF - Pharmacology Biochemistry and Behavior
IS - 1
ER -