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. Author manuscript; available in PMC: 2014 Jan 1.
Published in final edited form as: Psychopharmacology (Berl). 2012 Jul 25;225(1):127–140. doi: 10.1007/s00213-012-2801-2

Table 1.

Schedule of chronic exposure to escalating doses of heroin, extended withdrawal and chronic re-exposure to escalating doses of heroin (Heroin/Heroin group)

Dose (mg/kg) per injectiona Chronic Exposure to Escalating-Dose Heroinb Spontaneous Withdrawalc Chronic Exposure to Escalating-Dose Heroin

Time(h) 1 2 3 4 5 6 7 8 9 10 Day 11–20 21 22 23 24 25 26 27 28 29 30 31
0900 2.5 2.5 5 5 10 10 15 15 25 25 -- 2.5 2.5 5 5 10 10 15 15 25 25 **
1300 -- -- -- -- -- -- -- -- -- -- -- 0 0* 0 0* 0 0* 0 0* 0 0*
1500 2.5 2.5 5 5 10 10 15 15 25 25 -- 2.5* 2.5 5* 5 10* 10 15* 15 25* 25
2100 2.5 2.5 5 5 10 10 15 15 25 25 -- 2.5 2.5 5 5 10 10 15 15 25 25
Total 7.5 7.5 15 15 30 30 45 45 75 75 -- 7.5 7.5 15 15 30 30 45 45 75 75
a

Administered via intraperitoneal injection by the experimenter. Injections of saline vehicle are denoted by 0.

b

A separate group of rats (Saline/Heroin) received saline injections, rather than heroin injections, on an identical schedule on Days 1–10, followed by an injection-free period from Days 11–20. Heroin and saline injections, as well as timing of conditioning sessions, occurring on Days 21–30 were identical to those received by the Heroin/Heroin group.

c

Autoradiographic analyses were performed on rats that received chronic heroin exposure (Days 1–10) and extended withdrawal (Days 11–20), when they were sacrificed.

*

Injection was administered immediately before the rat was placed in the associated conditioning chamber of the place preference apparatus.

**

Conditioned place preference testing