-
Something wrong with this record ?
Nesfatin-1 influences the excitability of gastric distension-responsive neurons in the ventromedial hypothalamic nucleus of rats
H. Feng, Q. Wang, F. Guo, X. Han, M. Pang, X. Sun, Y. Gong, L. Xu
Language English Country Czech Republic
Document type Journal Article
NLK
Directory of Open Access Journals
from 1991
Free Medical Journals
from 1998
ProQuest Central
from 2005-01-01
Medline Complete (EBSCOhost)
from 2006-01-01
Nursing & Allied Health Database (ProQuest)
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- Action Potentials physiology MeSH
- DNA-Binding Proteins metabolism MeSH
- Gastrointestinal Motility physiology MeSH
- Corticotropin-Releasing Hormone metabolism MeSH
- Rats MeSH
- Neurons physiology MeSH
- Ventromedial Hypothalamic Nucleus physiology MeSH
- Rats, Wistar MeSH
- Nerve Tissue Proteins metabolism MeSH
- Calcium-Binding Proteins metabolism MeSH
- Stomach physiology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
The present study investigated the effects of nesfatin-1 on gastric distension (GD)-responsive neurons via an interaction with corticotropin-releasing factor (CRF) receptor signaling in the ventromedial hypothalamic nucleus (VMH), and the potential regulation of these effects by hippocampal projections to VMH. Extracellular single-unit discharges were recorded in VHM following administration of nesfatin-1. The projection of nerve fibers and expression of nesfatin-1 were assessed by retrograde tracing and fluoro-immunohistochemical staining, respectively. Results showed that there were GD-responsive neurons in VMH; Nesfatin-1 administration and electrical stimulation of hippocampal CA1 sub-region altered the firing rate of these neurons. These changes could be partially blocked by pretreatment with the non-selective CRF antagonist astressin-B or an antibody to NUCB2/nesfatin-1. Electrolytic lesion of CA1 hippocampus reduced the effects of nesfatin-1 on VMH GD-responsive neuronal activity. These studies suggest that nesfatin-1 plays an important role in GD-responsive neuronal activity through interactions with CRF signaling pathways in VMH. The hippocampus may participate in the modulation of nesfatin-1-mediated effects in VMH.
Department of Pathophysiology Medical College of Qingdao University Qingdao Shandong PR China
Otolaryngological Department Qingdao Municipal Hospital Qingdao Shandong PR China
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18011455
- 003
- CZ-PrNML
- 005
- 20180502083258.0
- 007
- ta
- 008
- 180405s2017 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.933347 $2 doi
- 035 __
- $a (PubMed)27982684
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Feng, Hongzhen $u Department of Pathophysiology, Medical College of Qingdao University, Qingdao, Shandong, PR China
- 245 10
- $a Nesfatin-1 influences the excitability of gastric distension-responsive neurons in the ventromedial hypothalamic nucleus of rats / $c H. Feng, Q. Wang, F. Guo, X. Han, M. Pang, X. Sun, Y. Gong, L. Xu
- 520 9_
- $a The present study investigated the effects of nesfatin-1 on gastric distension (GD)-responsive neurons via an interaction with corticotropin-releasing factor (CRF) receptor signaling in the ventromedial hypothalamic nucleus (VMH), and the potential regulation of these effects by hippocampal projections to VMH. Extracellular single-unit discharges were recorded in VHM following administration of nesfatin-1. The projection of nerve fibers and expression of nesfatin-1 were assessed by retrograde tracing and fluoro-immunohistochemical staining, respectively. Results showed that there were GD-responsive neurons in VMH; Nesfatin-1 administration and electrical stimulation of hippocampal CA1 sub-region altered the firing rate of these neurons. These changes could be partially blocked by pretreatment with the non-selective CRF antagonist astressin-B or an antibody to NUCB2/nesfatin-1. Electrolytic lesion of CA1 hippocampus reduced the effects of nesfatin-1 on VMH GD-responsive neuronal activity. These studies suggest that nesfatin-1 plays an important role in GD-responsive neuronal activity through interactions with CRF signaling pathways in VMH. The hippocampus may participate in the modulation of nesfatin-1-mediated effects in VMH.
- 650 _2
- $a akční potenciály $x fyziologie $7 D000200
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a proteiny vázající vápník $x metabolismus $7 D002135
- 650 _2
- $a hormon uvolňující kortikotropin $x metabolismus $7 D003346
- 650 _2
- $a DNA vazebné proteiny $x metabolismus $7 D004268
- 650 _2
- $a gastrointestinální motilita $x fyziologie $7 D005769
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a proteiny nervové tkáně $x metabolismus $7 D009419
- 650 _2
- $a neurony $x fyziologie $7 D009474
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a žaludek $x fyziologie $7 D013270
- 650 _2
- $a nucleus ventromedialis hypothalami $x fyziologie $7 D014697
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Wang, Qiaoling $u Department of Pathophysiology, Medical College of Qingdao University, Qingdao, Shandong, PR China
- 700 1_
- $a Guo, Feifei $u Department of Pathophysiology, Medical College of Qingdao University, Qingdao, Shandong, PR China
- 700 1_
- $a Han, Xiaohua $u Department of Pathophysiology, Medical College of Qingdao University, Qingdao, Shandong, PR China
- 700 1_
- $a Pang, Mingjie $u Otolaryngological Department, Qingdao Municipal Hospital (Group), Qingdao, Shandong, PR China
- 700 1_
- $a Sun, Xiangrong $u Department of Pathophysiology, Medical College of Qingdao University, Qingdao, Shandong, PR China
- 700 1_
- $a Gong, Yanling $u Department of Pharmacy, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, Shandong, PR China
- 700 1_
- $a Xu, Luo $u Department of Pathophysiology, Medical College of Qingdao University, Qingdao, Shandong, PR China
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 66, č. 2 (2017), s. 335-344
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/27982684 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20180405 $b ABA008
- 991 __
- $a 20180430105839 $b ABA008
- 999 __
- $a ok $b bmc $g 1296234 $s 1008267
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 66 $c 2 $d 335-344 $e 20161216 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- LZP __
- $b NLK118 $a Pubmed-20180405