PMID- 1967830 OWN - NLM STAT- MEDLINE DCOM- 19900306 LR - 20190501 IS - 0027-8424 (Print) IS - 1091-6490 (Electronic) IS - 0027-8424 (Linking) VI - 87 IP - 2 DP - 1990 Jan TI - Application of entropy measures derived from the ergodic theory of dynamical systems to rat locomotor behavior. PG - 723-7 AB - Measures of complexity derived from ergodic theory of dynamical systems were developed and applied to an exemplary data set describing locomotor movements of rats in a bounded space. A symbolic dynamical system was obtained by partitioning the event space into equally probable partition elements, using a k-dimensional tree. The measures calculated from the symbolic sequences included the topological entropy (ht)--i.e., the rate of increase of all possible sequences with increasing sequence length--and the metric entropy (hm)--i.e., the rate of increase of all likely sequences with increasing sequence length. These measures were used to assess changes in rat locomotor behavior as recorded in the behavioral pattern monitor (BPM) that were induced by amphetamine (0.25, 0.50, 1.0, or 2.0 mg/kg) and 3,4-methylenedioxymethamphetamine (MDMA; 1.25, 2.5, 5.0, or 10.0 mg/kg). Amphetamine increased the mean activity, ht, and hm. MDMA resulted in a monotonic dose-response curve for activity but exhibited a biphasic dose response in ht and hm. In particular, some animals in the higher dose groups showed a ht in the range of the saline controls, whereas other animals exhibited a significantly reduced ht and a greater decrease in hm, suggesting that two different behavioral reactions coexist within the same higher dose range of MDMA. An important implication of our method is that, in applied ergodic measure-theoretic approaches, the partition that determines the elements of the symbolic dynamical system should not be specified a priori on abstract mathematical grounds but should be chosen relative to its significance with respect to the data set in question. Here, the animal constructs its own spatiotemporal partition in behavioral phase space. FAU - Paulus, M P AU - Paulus MP AD - Laboratory of Biological Dynamics and Theoretical Medicine, School of Medicine, University of California, San Diego, La Jolla 92093. FAU - Geyer, M A AU - Geyer MA FAU - Gold, L H AU - Gold LH FAU - Mandell, A J AU - Mandell AJ LA - eng GR - DA02925/DA/NIDA NIH HHS/United States GR - MH00188/MH/NIMH NIH HHS/United States GR - MH16109/MH/NIMH NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Proc Natl Acad Sci U S A JT - Proceedings of the National Academy of Sciences of the United States of America JID - 7505876 RN - 0 (Designer Drugs) RN - 4764-17-4 (3,4-Methylenedioxyamphetamine) RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) RN - TZ47U051FI (Dextroamphetamine) SB - IM MH - 3,4-Methylenedioxyamphetamine/analogs & derivatives/pharmacology MH - Animals MH - Designer Drugs MH - Dextroamphetamine/pharmacology MH - Male MH - Mathematics MH - *Models, Neurological MH - *Motor Activity/drug effects MH - N-Methyl-3,4-methylenedioxyamphetamine MH - Rats MH - Rats, Inbred Strains MH - Reference Values PMC - PMC53338 EDAT- 1990/01/01 00:00 MHDA- 1990/01/01 00:01 PMCR- 1990/07/01 CRDT- 1990/01/01 00:00 PHST- 1990/01/01 00:00 [pubmed] PHST- 1990/01/01 00:01 [medline] PHST- 1990/01/01 00:00 [entrez] PHST- 1990/07/01 00:00 [pmc-release] AID - 10.1073/pnas.87.2.723 [doi] PST - ppublish SO - Proc Natl Acad Sci U S A. 1990 Jan;87(2):723-7. doi: 10.1073/pnas.87.2.723.