scholarly journals Pallial origin of basal forebrain cholinergic neurons in the nucleus basalis of Meynert and horizontal limb of the diagonal band nucleus

Development ◽  
2011 ◽  
Vol 138 (19) ◽  
pp. 4315-4326 ◽  
Author(s):  
A. Pombero ◽  
C. Bueno ◽  
L. Saglietti ◽  
M. Rodenas ◽  
J. Guimera ◽  
...  
Keyword(s):  
Basal Forebrain ◽  
Cholinergic Neurons ◽  
Nucleus Basalis ◽  
Nucleus Basalis Of Meynert ◽  
Diagonal Band ◽  
Basal Forebrain Cholinergic Neurons

scholarly journals Basal forebrain cholinergic neurons are part of the threat memory engram

2021 ◽  
Author(s):  
Prithviraj Rajebhosale ◽  
Mala R Ananth ◽  
Richard B Crouse ◽  
Li Jiang ◽  
Gretchen López- Hernández ◽  
...  
Keyword(s):  
Basal Forebrain ◽  
Basolateral Amygdala ◽  
Cholinergic Neurons ◽  
Nucleus Basalis ◽  
Early Gene ◽  
Intrinsic Excitability ◽  
Cholinergic Basal Forebrain ◽  
Basal Forebrain Cholinergic Neurons ◽  
Cholinergic Signaling ◽  
Memory Engram

Although the engagement of cholinergic signaling in threat memory is well established (Knox, 2016a), our finding that specific cholinergic neurons are requisite partners in a threat memory engram is likely to surprise many. Neurons of the basal forebrain nucleus basalis and substantia innonimata (NBM/SIp) comprise the major source of cholinergic input to the basolateral amygdala (BLA), whose activation are required for both the acquisition and retrieval of cued threat memory and innate threat response behavior. The retrieval of threat memory by the presentation of the conditioning tone alone elicits acetylcholine (ACh) release in the BLA and the BLA-projecting cholinergic neurons manifest immediate early gene responses and display increased intrinsic excitability for 2-5 hours following the cue-elicited memory response to the conditioned stimulus. Silencing cue-associated engram-enrolled cholinergic neurons prevents the expression of the defensive response and the subset of cholinergic neurons activated by cue is distinct from those engaged by innate threat. Taken together we find that distinct populations of cholinergic neurons are recruited to signal distinct aversive stimuli via the BLA, demonstrating exquisite, functionally refined organization of specific types of memory within the cholinergic basal forebrain.

scholarly journals Estimation of the Total Number of Cholinergic Neurons Containing Estrogen Receptor-α in the Rat Basal Forebrain

2002 ◽  
Vol 50 (7) ◽  
pp. 891-902 ◽  
Author(s):  
Riitta A. Miettinen ◽  
Giedrius Kalesnykas ◽  
Esa H. Koivisto
Keyword(s):  
Estrogen Receptor ◽  
Basal Forebrain ◽  
Cholinergic Neurons ◽  
Estrogen Receptor Α ◽  
Medial Septum ◽  
Nucleus Basalis ◽  
Cell Counting ◽  
Double Immunostaining ◽  
Diagonal Band ◽  
Diagonal Band Of Broca

This study was undertaken to estimate the total number of cholinergic cells and the percentage of cholinergic cells that contain estrogen receptor-α (ERα) in the rat basal forebrain. Double immunostaining for choline acetyltransferase (ChAT) and ERα was carried out on 50-μm-thick free-floating sections. Because routine mounting method causes considerable flattening of the sections, we embedded immunostained sections in Durcupan, an epoxy resin known to cause virtually no shrinkage. When this procedure was used the section thickness was well preserved, individual cells could be clearly identified, and subcellular localization of ERα immunoreactivity was easy to verify. Cell counting in these sections revealed that the rat basal forebrain contains 26,390 ± 1097 (mean ± SEM) cholinergic neurons. This comprises 9674 ± 504 in the medial septum-vertical diagonal band of Broca, 9403 ± 484 in the horizontal diagonal band of Broca, and 7312 ± 281 in the nucleus basalis. In these nuclei, 60%, 46%, and 14% of the cholinergic neurons were colocalized with ERα, respectively. We believe that our results are an improvement on existing data because of the better distinction of individual neurons that the Durcupan embedding method brings.

scholarly journals Estradiol Modulation of Neurotrophin Receptor Expression in Female Mouse Basal Forebrain Cholinergic Neurons In Vivo

Endocrinology ◽  
2014 ◽  
Vol 156 (2) ◽  
pp. 613-626 ◽  
Author(s):  
Michael R. Milne ◽  
Christopher A. Haug ◽  
István M. Ábrahám ◽  
Andrea Kwakowsky
Keyword(s):  
Estrogen Receptor ◽  
Choline Acetyltransferase ◽  
Basal Forebrain ◽  
Neuroprotective Effect ◽  
Cholinergic Neurons ◽  
Receptor Expression ◽  
Nucleus Basalis ◽  
Neurotrophin Receptor ◽  
Ovariectomized Mice ◽  
Basal Forebrain Cholinergic Neurons

The neuroprotective effect of estradiol (E2) on basal forebrain cholinergic neurons (BFCNs) has been suggested to occur as a result of E2 modulation of the neurotrophin system on these neurons. The present study provides a comprehensive examination of the relationship between E2 and neurotrophin signaling on BFCNs by investigating the effect of E2 deficiency on the expression levels of neurotrophin receptors (NRs), TrkA, TrkB, and p75 on BFCNs. The number of TrkA receptor-expressing choline acetyltransferase-positive neurons was significantly reduced in the medial septum (MS) in the absence of E2. A significant reduction in TrkB-expressing choline acetyltransferase-positive cells was also observed in ovariectomized mice in the MS and nucleus basalis magnocellularis (NBM). p75 receptor expression was reduced in the NBM and striatum but not in the MS. We also showed that estrogen receptor (ER)-α was expressed by a small percentage of TrkA- and TrkB-positive neurons in the MS (12%) and NBM (19%) and by a high percentage of TrkB-positive neurons in the striatum (69%). Similarly, ERα was expressed at low levels by p75 neurons in the MS (6%) and NBM (9%) but was not expressed on striatal neurons. Finally, ERα knockout using neuron-specific estrogen receptor-α knockout transgenic mice abolished all E2-mediated changes in the NR expression on BFCNs. These results indicate that E2 differentially regulates NR expression on BFCNs, with effects depending on the NR type and neuroanatomical location, and also provide some evidence that alterations in the NR expression are, at least in part, mediated via ERα.

scholarly journals Hydrophilic cell-derived extracellular matrix as a niche to promote adhesion and differentiation of neural progenitor cells

RSC Advances ◽  
2017 ◽  
Vol 7 (72) ◽  
pp. 45587-45594 ◽  
Author(s):  
Lingyan Yang ◽  
Ziyun Jiang ◽  
Linhong Zhou ◽  
Keli Zhao ◽  
Xun Ma ◽  
...  
Keyword(s):  
Extracellular Matrix ◽  
Basal Forebrain ◽  
Progenitor Cell ◽  
Neural Progenitor Cells ◽  
Cholinergic Neurons ◽  
Neural Progenitor Cell ◽  
Neural Progenitor ◽  
Basal Forebrain Cholinergic Neurons ◽  
Adhesion Performance ◽  
Excellent Adhesion

Cell-derived extracellular matrix exhibits excellent adhesion performance for neural progenitor cell anchoring and residency, resulting in promoted proliferation of the stem cells to basal forebrain cholinergic neurons.

PACAP has a neurotrophic effect on cultured basal forebrain cholinergic neurons from adult rats

2001 ◽  
Vol 131 (1-2) ◽  
pp. 41-45 ◽  
Author(s):  
Aki Yuhara ◽  
Chika Nishio ◽  
Yasuhiro Abiru ◽  
Hiroshi Hatanaka ◽  
Nobuyuki Takei
Keyword(s):  
Basal Forebrain ◽  
Cholinergic Neurons ◽  
Adult Rats ◽  
Neurotrophic Effect ◽  
Basal Forebrain Cholinergic Neurons
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