Author(s): Logan CG, Grafton ST
Relative cerebral glucose metabolism was examined with positron-emission tomography (PET) as a measure of neuronal activation during performance of the classically conditioned eyeblink response in 12 young adult subjects. Each subject received three sessions: (i) a control session with PET scan in which unpaired presentations of the tone conditioned stimulus and corneal airpuff unconditioned stimulus were administered, (ii) a paired training session to allow associative learning to occur, and (iii) a paired test session with PET scan. Brain regions exhibiting learning-related activation were identified as those areas that showed significant differences in glucose metabolism between the unpaired control condition and well-trained state in the 9 subjects who met the learning criterion. Areas showing significant activation included bilateral sites in the inferior cerebellar cortex/deep nuclei, anterior cerebellar vermis, contralateral cerebellar cortex and pontine tegmentum, ipsilateral inferior thalamus/red nucleus, ipsilateral hippocampal formation, ipsilateral lateral temporal cortex, and bilateral ventral striatum. Among all subjects, including those who did not meet the learning criterion, metabolic changes in ipsilateral cerebellar nuclei, bilateral cerebellar cortex, anterior vermis, contralateral pontine tegmentum, ipsilateral hippocampal formation, and bilateral striatum correlated with degree of learning. The localization to cerebellum and its associated brainstem circuitry is consistent with neurobiological studies in the rabbit model of eyeblink classical conditioning and neuropsychological studies in brain-damaged humans. In addition, these data support a role for the hippocampus in conditioning and suggest that the ventral striatum may also be involved.
Referred From: https://www.ncbi.nlm.nih.gov/pubmed/7638220
Author(s): Lu X, Miyachi S, Ito Y, Nambu A, Takada M
Author(s): Lu X, Miyachi S, Takada M
Author(s): McCormick DA, Thompson RF
Author(s): Gerwig M, Haerter K, Hajjar K, Dimitrova A, Maschke M, et al.
Author(s): Blaxton TA, Zeffiro TA, Gabrieli JD, Bookheimer SY, Carrillo MC, et al.
Author(s): Schreurs BG, McIntosh AR, Bahro M, Herscovitch P, Sunderland T, et al.
Author(s): Molchan SE, Sunderland T, McIntosh AR, Herscovitch P, Schreurs BG
Author(s): Lu X, Hikosaka O, Miyachi S
Author(s): Gruart A , Guillazo-Blanch G, Fernandez-Mas R, Jimenez-Diaz L, Delgado-Garcia JM
Author(s): Park JS, Onodera T, Nishimura S, Thompson RF, Itohara S
Author(s): Lavond DG, Hembree TL, Thompson RF
Author(s): Skelton RW
Author(s): Steinmetz JE, Lavond DG, Ivkovich D, Logan CG, Thompson RF
Author(s): Woodruff-Pak DS, Lavond DG, Logan CG, Steinmetz JE, Thompson RF
Author(s): Swain RA, Shinkman PG, Thompson JK, Grethe JS, Thompson RF
Author(s): Chapman PF, Steinmetz JE, Sears LL, Thompson RF
Author(s): Bao S, Chen L, Kim JJ, Thompson RF
Author(s): Kleim JA, Freeman JH Jr, Bruneau R, Nolan BC, Cooper NR, et al.
Author(s): Miller MJ, Chen NK, Li L, Tom B, Weiss C, et al.
Author(s): Hikosaka O, Nakahara H, Rand MK, Lu X, Nakamura K, et al.
Author(s): Lu X, Ashe J
Author(s): Ashe J, Lungu OV, Basford, AT, Lu X
Author(s): Nawrot M, Rizzo M
Author(s): Nawrot M, Rizzo M
Author(s): Schmahmann JD, Sherman JC.
Author(s): Thier P, Haarmeier T, Treue S, Barash S
Author(s): Jokisch D, Troje NF, Koch B, Schwarz M, Daum I
Author(s): Maschke M, Gomez CM, Tuite PJ, Pickett K, Konczak J
Author(s): Ravizza SM, McCormick CA, Schlerf JE, Justus T, Ivry RB, et al.
Author(s): Haarmeier T, Thier P
Author(s): Richter S, Gerwig M, Aslan B, Wilhelm H, Schoch B, et al.
Author(s): Ritvo ER, Freeman BJ, Scheibel AB, Duong T, Robinson H, et al.