TY - JOUR
T1 - Simple apparatus for serial blood sampling in rodents permitting simultaneous measurement of locomotor activity as illustrated with cocaine
AU - Hutchaleelaha, Athiwat
AU - Sukbuntherng, Juthamas
AU - Mayersohn, Michael
N1 - Funding Information:
The authors gratefully acknowledge financial support for this research from the National Institute on Drug Abuse (DA 08094). We also wish to thank Tongjit Tieophanitjaroen and Yupiradee Chinnasote for sketching the experimental diagram and Debbie Martin for her technical assistance.
PY - 1997/2
Y1 - 1997/2
N2 - A simple device has been developed for serial venous blood sampling which permits the simultaneous measurement of locomotor activity in the freely moving rat. The device can be easily constructed from routine laboratory material and it does not interfere with the light beams used to measure locomotor activity. The device, in conjunction with an activity cage, has been applied to the combined pharmacokinetic and pharmacodynamic modeling of cocaine. The relationship between the locomotor activity following a single short iv infusion of cocaine (5 mg/kg) and cocaine plasma concentrations can be adequately described by the Sigmoid-E(max) model. Further, the relationship between activity and time can be described by the same model coupled with an effect compartment. These results suggest the applicability of the device in facilitating pharmacokinetic/pharmacodynamic modeling of drugs that affect locomotor activity.
AB - A simple device has been developed for serial venous blood sampling which permits the simultaneous measurement of locomotor activity in the freely moving rat. The device can be easily constructed from routine laboratory material and it does not interfere with the light beams used to measure locomotor activity. The device, in conjunction with an activity cage, has been applied to the combined pharmacokinetic and pharmacodynamic modeling of cocaine. The relationship between the locomotor activity following a single short iv infusion of cocaine (5 mg/kg) and cocaine plasma concentrations can be adequately described by the Sigmoid-E(max) model. Further, the relationship between activity and time can be described by the same model coupled with an effect compartment. These results suggest the applicability of the device in facilitating pharmacokinetic/pharmacodynamic modeling of drugs that affect locomotor activity.
KW - Blood sampling device
KW - Cocaine
KW - Locomotor activity
KW - Pharmacokinetic/pharmacodynamic modeling
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U2 - 10.1016/S1056-8719(96)00142-6
DO - 10.1016/S1056-8719(96)00142-6
M3 - Article
C2 - 9086283
AN - SCOPUS:0030951774
SN - 1056-8719
VL - 37
SP - 9
EP - 14
JO - Journal of Pharmacological and Toxicological Methods
JF - Journal of Pharmacological and Toxicological Methods
IS - 1
ER -