Postnatal development of CA3 pyramidal neurons and their afferents in the Ammon's horn of rhesus monkeys

Hippocampus ◽  
1995 ◽  
Vol 5 (3) ◽  
pp. 217-231 ◽  
Author(s):  
László Seress ◽  
Charles E. Ribak
QJM ◽  
2020 ◽  
Vol 113 (Supplement_1) ◽  
Author(s):  
A A A Baraka ◽  
K A Hafez ◽  
A I A Othman ◽  
A M M Sadek

Abstract Introduction In recent year deterioration in cognitive, learning, and memory become one of the significant problems in human life. Hippocampus is a pivotal part of the brain’s limbic system which serves a critical role in memory, learning process and regulating the emotions. In most regions of the brain, neurons are generated only at specific periods of early development, and not born in the adulthood. In contrast, hippocampal neurons are generated throughout development and adult life. The hippocampal dentate gyrus was reported to be one of the few regions of the mammalian brain where neurogenesis continue to occur throughout adulthood. The neurogenesis in the dentate gyrus was thought to play an important role in hippocampus-dependent learning and memory. The hippocampal formation is composed of the hippocampus proper, the dentate gyrus and the subiculum. The hippocampus proper is the largest part and is subdivided into fields designated as Cornu Ammonis or Ammon’s horn (CA) from CA1 to CA4. Ammon's horn is continuous with the subiculum, which acts as the main output source of the hippocampal formation. Aim of the Study To study the postnatal development of the hippocampal formation. Materials and Methods Five male albino rats from the following postnatal ages day 1, week 1, week 2, week3 and week 4 were studied by histological, immunohistochemical, and morphometric methods. Results The general architecture of the hippocampus proper with its polymorphic, pyramidal, and molecular layers was present at day1, whereas the details of the adult structure appeared at week 2. In the dentate gyrus, distinct lamination appeared at week 1 and its maturation continued with the production of neurons at the interhilar zone that peaked at week 2. The number and density of pyramidal axons and dendrites increase by age. Astrocytes increased in size and staining affinity for glial filaments, and acquired a stellate shape with age. Furthermore, the number of granule cell layers increased concomitantly with the increase in thickness of the molecular and polymorphic layers of both the hippocampus proper and the dentate gyrus. Conclusion The important sequences of events in the growth and maturation of the hippocampal formation in male albino rat occurred in the first 2 postnatal weeks.


1996 ◽  
Vol 733 (1) ◽  
pp. 31-40 ◽  
Author(s):  
R. Roy Vaid ◽  
Benjamin K. Yee ◽  
J.N.P. Rawlins ◽  
Susan Totterdell

1990 ◽  
Vol 115 (2-3) ◽  
pp. 161-166 ◽  
Author(s):  
Tadashi Ino ◽  
Shigeru Matsuzaki ◽  
Yasuhide Shinonaga ◽  
Hitoshi Ohishi ◽  
Reiko Ogawa-Meguro ◽  
...  

1990 ◽  
Vol 11 ◽  
pp. S53
Author(s):  
Tadashi Ino ◽  
Shigeru Matsuzaki ◽  
Hitoshi Ohishi ◽  
Sakashi Nomura ◽  
Noboru Mizuno

1990 ◽  
Vol 15 ◽  
pp. S53
Author(s):  
Tadashi Ino ◽  
Shigeru Matsuzaki ◽  
Hitoshi Ohishi ◽  
Sakashi Nomura ◽  
Noboru Mizuno

1995 ◽  
Vol 73 (1) ◽  
pp. 246-255 ◽  
Author(s):  
J. L. Gaiarsa ◽  
V. Tseeb ◽  
Y. Ben-Ari

1. Intracellular recordings were made from adult and neonatal rat hippocampal slices to study the postnatal development of GABAB-mediated inhibition in CA3 pyramidal neurons. 2. In the presence of glutamatergic receptor antagonists, direct electrical stimulation of the interneurons induced a biphasic GABAA- and GABAB-mediated inhibitory postsynaptic potential in adult [postnatal day (P) 30-P40] and young (P6-P8) CA3 pyramidal neurons. In contrast, in pups (P0-P3), electrical stimulation only induced a bicuculline-sensitive depolarizing GABAA synaptic potential. 3. The outward postsynaptic currents generated by bath-applications of baclofen (30 microM, 30 s) at P3 (78 +/- 60 pA, mean +/- SE) were 4 to 5 times smaller than those evoked between P6 (329 +/- 32 pA) and P30 (412 +/- 44 pA). At P0, baclofen failed to induce a postsynaptic current. 4. The outward currents generated by serotonin (50 microM, 30 s) and the A1 receptor agonist N-cyclopentyladenosine (40 microM, 30 s) ranged between 0 and 50 pA at P3 and between 200 and 400 pA at P6 and P30 (holding potential = -60 +/- 2 mV). 5. In the presence of potassium channel blockers, the amplitude of calcium current elicited by a depolarizing voltage step command (1 s) from a holding potential of -60 mV to a test potential of 0 mV was 2 +/- 0.15 nA at P6 (n = 9) and 0.73 +/- 0.14 nA at P3 (n = 8). Baclofen reversibly reduced the amplitude of calcium currents in young rats but not in pups. 6. Baclofen reversibly reduced the amplitude of the evoked GABAA-mediated and glutamatergic synaptic events at all developmental stages. These effects were dose dependent and antagonized by P-alpha 3-aminopropyl-P-diethoxymethyl-phosphinic acid (CGP) 35348 (500 microM). 7. We conclude that postsynaptic GABAB-mediated inhibition is absent or minimal during the first postnatal days in the CA3 region. In contrast, presynaptic GABAB inhibition is present at birth. We discuss the mechanisms and physiological consequences of these observations.


1988 ◽  
Vol 460 (1) ◽  
pp. 173-177 ◽  
Author(s):  
Tadashi Ino ◽  
Kazuo Itoh ◽  
Hiroto Kamiya ◽  
Ryuichi Shigemoto ◽  
Ichiro Akiguchi ◽  
...  

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