Abstract
Synapses are essential to neuronal functions. Synaptic changes occur under physiological and pathological conditions. Here we report the remodeling of synapses in the CA1 area of the hippocampus after transient global ischemia using electron microscopy. Much electron-dense material appeared in the cytoplasm of dendrites at 24. h after ischemia. Many dark axons or terminals were found in the CA1 neuropil; some of which were phagocytized by dendrites. Interestingly autophagosomes appeared in many axons or dendrites at 48. h after ischemia. In addition, postsynaptic density (PSD) - like structures or synaptic - like structures were found inside spines and dendrites. Statistical analysis demonstrated that the thickness of PSDs in the CA1 neuropil increased from 12 to 48. h after ischemia. The frequency of autophagosomes appeared to escalate from 12 to 48. h after ischemia. The frequency of asymmetric synapses was significantly increased at 12. h and 24. h after ischemia in stratum oriens, proximal and distal stratum radiatum. Among asymmetric synapses, the number of perforated synapses consistently increased and reached a peak (approximately 10-fold increase) at 48. h after ischemia. On the other hand, the number of multiple synaptic boutons decreased after ischemia reaching a two to fourfold decrease at 48. h after ischemia. These results have shown that ischemia induces an increase of asymmetric synapses as well as synaptic autophagy, which may contribute to the neuronal death in the CA1 area after transient global ischemia.
Original language | English |
---|---|
Pages (from-to) | 268-277 |
Number of pages | 10 |
Journal | Neuroscience |
Volume | 218 |
DOIs | |
State | Published - Aug 30 2012 |
Fingerprint
Keywords
- Asymmetric synapses
- Autophagy
- Axonal degeneration
- Hippocampus
- Ischemia
- Synaptic remodeling
ASJC Scopus subject areas
- Neuroscience(all)
Cite this
Remodeling of synapses in the CA1 area of the hippocampus after transient global ischemia. / Ruan, Y. W.; Han, X. J.; Shi, Z. S.; Lei, Z. G.; Xu, Z. C.
In: Neuroscience, Vol. 218, 30.08.2012, p. 268-277.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Remodeling of synapses in the CA1 area of the hippocampus after transient global ischemia
AU - Ruan, Y. W.
AU - Han, X. J.
AU - Shi, Z. S.
AU - Lei, Z. G.
AU - Xu, Z. C.
PY - 2012/8/30
Y1 - 2012/8/30
N2 - Synapses are essential to neuronal functions. Synaptic changes occur under physiological and pathological conditions. Here we report the remodeling of synapses in the CA1 area of the hippocampus after transient global ischemia using electron microscopy. Much electron-dense material appeared in the cytoplasm of dendrites at 24. h after ischemia. Many dark axons or terminals were found in the CA1 neuropil; some of which were phagocytized by dendrites. Interestingly autophagosomes appeared in many axons or dendrites at 48. h after ischemia. In addition, postsynaptic density (PSD) - like structures or synaptic - like structures were found inside spines and dendrites. Statistical analysis demonstrated that the thickness of PSDs in the CA1 neuropil increased from 12 to 48. h after ischemia. The frequency of autophagosomes appeared to escalate from 12 to 48. h after ischemia. The frequency of asymmetric synapses was significantly increased at 12. h and 24. h after ischemia in stratum oriens, proximal and distal stratum radiatum. Among asymmetric synapses, the number of perforated synapses consistently increased and reached a peak (approximately 10-fold increase) at 48. h after ischemia. On the other hand, the number of multiple synaptic boutons decreased after ischemia reaching a two to fourfold decrease at 48. h after ischemia. These results have shown that ischemia induces an increase of asymmetric synapses as well as synaptic autophagy, which may contribute to the neuronal death in the CA1 area after transient global ischemia.
AB - Synapses are essential to neuronal functions. Synaptic changes occur under physiological and pathological conditions. Here we report the remodeling of synapses in the CA1 area of the hippocampus after transient global ischemia using electron microscopy. Much electron-dense material appeared in the cytoplasm of dendrites at 24. h after ischemia. Many dark axons or terminals were found in the CA1 neuropil; some of which were phagocytized by dendrites. Interestingly autophagosomes appeared in many axons or dendrites at 48. h after ischemia. In addition, postsynaptic density (PSD) - like structures or synaptic - like structures were found inside spines and dendrites. Statistical analysis demonstrated that the thickness of PSDs in the CA1 neuropil increased from 12 to 48. h after ischemia. The frequency of autophagosomes appeared to escalate from 12 to 48. h after ischemia. The frequency of asymmetric synapses was significantly increased at 12. h and 24. h after ischemia in stratum oriens, proximal and distal stratum radiatum. Among asymmetric synapses, the number of perforated synapses consistently increased and reached a peak (approximately 10-fold increase) at 48. h after ischemia. On the other hand, the number of multiple synaptic boutons decreased after ischemia reaching a two to fourfold decrease at 48. h after ischemia. These results have shown that ischemia induces an increase of asymmetric synapses as well as synaptic autophagy, which may contribute to the neuronal death in the CA1 area after transient global ischemia.
KW - Asymmetric synapses
KW - Autophagy
KW - Axonal degeneration
KW - Hippocampus
KW - Ischemia
KW - Synaptic remodeling
UR - http://www.scopus.com/inward/record.url?scp=84863778245&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84863778245&partnerID=8YFLogxK
U2 - 10.1016/j.neuroscience.2012.05.035
DO - 10.1016/j.neuroscience.2012.05.035
M3 - Article
C2 - 22634576
AN - SCOPUS:84863778245
VL - 218
SP - 268
EP - 277
JO - Neuroscience
JF - Neuroscience
SN - 0306-4522
ER -