PMID- 12455007 OWN - NLM STAT- MEDLINE DCOM- 20030122 LR - 20181113 IS - 0021-9967 (Print) IS - 1096-9861 (Electronic) IS - 0021-9967 (Linking) VI - 454 IP - 4 DP - 2002 Dec 23 TI - Structural and functional asymmetry in the normal and epileptic rat dentate gyrus. PG - 424-39 AB - The rat dentate gyrus is usually described as relatively homogeneous. Here, we present anatomic and physiological data which demonstrate that there are striking differences between the supra- and infrapyramidal blades after status epilepticus and recurrent seizures. These differences appear to be an accentuation of a subtle asymmetry present in normal rats. In both pilocarpine and kainic acid models, there was greater mossy fiber sprouting in the infrapyramidal blade. This occurred primarily in the middle third of the hippocampus. Asymmetric sprouting was evident both with Timm stain as well as antisera to brain-derived neurotrophic factor (BDNF) or neuropeptide Y (NPY). In addition, surviving NPY-immunoreactive hilar neurons were distributed preferentially in the suprapyramidal region of the hilus. Extracellular recordings from infrapyramidal sites in hippocampal slices of pilocarpine-treated rats showed larger population spikes and weaker paired-pulse inhibition in response to perforant path stimulation relative to suprapyramidal recordings. A single stimulus could evoke burst discharges in infrapyramidal granule cells but not suprapyramidal blade neurons. BDNF exposure led to spontaneous epileptiform discharges that were larger in amplitude and longer lasting in the infrapyramidal blade. Stimulation of the infrapyramidal molecular layer evoked larger responses in area CA3 than suprapyramidal stimulation. In slices from the temporal pole, in which anatomic evidence of asymmetry waned, there was little evidence of physiological asymmetry either. Of interest, some normal rats also showed signs of greater evoked responses in the infrapyramidal blade, and this could be detected with both microelectrode recording and optical imaging techniques. Although there were no signs of hyperexcitability in normal rats, the data suggest that there is some asymmetry in the normal dentate gyrus and this asymmetry is enhanced by seizures. Taken together, the results suggest that supra- and infrapyramidal blades of the dentate gyrus could have different circuit functions and that the infrapyramidal blade may play a greater role in activating the hippocampus. CI - Copyright 2002 Wiley-Liss, Inc. FAU - Scharfman, Helen E AU - Scharfman HE AD - Center for Neural Recovery and Rehabilitation Research, Helen Hayes Hospital, West Haverstraw, New York 10993-1195, USA. scharfmanh@helenhayeshosp.org FAU - Sollas, Anne L AU - Sollas AL FAU - Smith, Karen L AU - Smith KL FAU - Jackson, Meyer B AU - Jackson MB FAU - Goodman, Jeffrey H AU - Goodman JH LA - eng GR - NS38285/NS/NINDS NIH HHS/United States GR - R56 NS037562/NS/NINDS NIH HHS/United States GR - R01 NS037562-04/NS/NINDS NIH HHS/United States GR - R01 NS037562/NS/NINDS NIH HHS/United States GR - NS37212/NS/NINDS NIH HHS/United States GR - NS37562/NS/NINDS NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Comp Neurol JT - The Journal of comparative neurology JID - 0406041 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Excitatory Amino Acid Agonists) RN - 0 (Muscarinic Agonists) RN - 0 (Neuropeptide Y) RN - 01MI4Q9DI3 (Pilocarpine) RN - SIV03811UC (Kainic Acid) SB - IM MH - Animals MH - Brain-Derived Neurotrophic Factor/analysis MH - Dentate Gyrus/*anatomy & histology/pathology/*physiology/physiopathology MH - Electrophysiology MH - Excitatory Amino Acid Agonists MH - Immunohistochemistry MH - Kainic Acid MH - Male MH - Mossy Fibers, Hippocampal/anatomy & histology/pathology/physiology/physiopathology MH - Muscarinic Agonists MH - Neuropeptide Y/analysis MH - Pilocarpine MH - *Rats MH - Rats, Sprague-Dawley MH - Seizures/pathology/physiopathology MH - Status Epilepticus/chemically induced/*pathology/*physiopathology MH - Synapses/pathology/physiology PMC - PMC2519114 MID - NIHMS59824 EDAT- 2002/11/28 04:00 MHDA- 2003/01/23 04:00 PMCR- 2008/08/23 CRDT- 2002/11/28 04:00 PHST- 2002/11/28 04:00 [pubmed] PHST- 2003/01/23 04:00 [medline] PHST- 2002/11/28 04:00 [entrez] PHST- 2008/08/23 00:00 [pmc-release] AID - 10.1002/cne.10449 [doi] PST - ppublish SO - J Comp Neurol. 2002 Dec 23;454(4):424-39. doi: 10.1002/cne.10449.