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The three main afferent systems, the commissural/associational path, the medial and the lateral perforant path, terminate in a strictly laminated fashion in the inner, middle, and outer molecular layer, respectively. , 2007). , 1990), calculated using the spine density estimates of Hama et al. (1989, see above), are 3,250, 2,780, and 2,600. Thus, the number of excitatory synapses onto a single GC could be as high as 8,630. The distribution of inhibitory terminals was analyzed in a combined immunocytochemical and electron microscopic study (Halasy and Somogyi, 1993a).

Pyramidale and often two or three apical dendrites emerge from the apical pole of the elongated soma. Finally, proximal dendrites of CA3 pyramidal cells bear large complex spines (“thorny excrescences”). These complex spines are the post- 34 I. Vida Fig. 3 Distribution of synapses on the dendrites of CA1 pyramidal cells. The drawing illustrates the subclasses of dendrites distinguished in the study by Meg´ıas et al. (2001). In the str. oriens, two types of dendritic processes were classified: first-order proximal basal dendrites with low spine density (oriens/proximal) and higher order distal dendrites with high spine density (oriens/distal).

6 μm−2 in the str. lacunosum-moleculare (Bannister and Larkman, 1995b). 5% Pyapali et al. 1% Pyapali et al. (1998) Sprague-Dawley, 2–8 months In vivo labeling Total 11,915 ± 1,030 L-M 2,259 ± 526 19% Rad 4,118 ± 1,203 35% Ori/Pyr 5,538 ± 943 47% Total 17,400 ± 6,200 Total L-M Rad Ori 11,549 ± 2,010 2,712 ± 873 4,638 ± 1,022 4,198 ± 1,056 Ishizuka et al. (1995) Sprague-Dawley, 33–57 days In vitro labeling 28,860 ± 3,102 Bannister and Larkman (1995a, b) Sprague-Dawley, male, 100–150 g In vitro labeling 36,100 ± 17,000 Cannon et al.

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