Species Diversity and Peptide Toxins Blocking Selectivity of Ether-à-go-go-Related Gene Subfamily K+ Channels in the Central Nervous System

2006 ◽  
Vol 69 (5) ◽  
pp. 1673-1683 ◽  
Author(s):  
Rita Restano-Cassulini ◽  
Yuliya V. Korolkova ◽  
Sylvie Diochot ◽  
Georgina Gurrola ◽  
Leonardo Guasti ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Species Diversity ◽  
Related Gene ◽  
K Channels ◽  
The Central Nervous System ◽  
Peptide Toxins ◽  
Gene Subfamily

Afferent and Efferent Synaptic Transmissions in Hair Cells

Physiology ◽  
1996 ◽  
Vol 11 (4) ◽  
pp. 161-166
Author(s):  
H Ohmori
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Synaptic Transmission ◽  
Nerve Terminal ◽  
Hair Cells ◽  
Electrical Signal ◽  
Membrane Hyperpolarization ◽  
K Channels ◽  
The Central Nervous System ◽  
Mechanical Information

Hair cells transduce mechanical information into electrical signal and, via afferent synapse, transmit it to the central nervous system (CNS). Hair cells receive cholinergic efferent innervation from the CNS, and a long-lasting membrane hyperpolarization is produced by activation of Ca2+-activated K+ channels. Acetylcholine may facilitate afferent synaptic transmission by suppressing K+ channels on the afferent nerve terminal.

scholarly journals Benefit of a single simulated hypobaric hypoxia in healthy mice performance and analysis of mitochondria-related gene changes

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Fei-Fei Wu ◽  
Kun-Long Zhang ◽  
Zheng-Mei Wang ◽  
Yi Yang ◽  
Shao-Hua Li ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Hypobaric Hypoxia ◽  
Video Tracking ◽  
Mild Stress ◽  
Behavioral Tests ◽  
Related Gene ◽  
Severe Hypobaric Hypoxia ◽  
The Central Nervous System ◽  
Gastrocnemius Muscles

AbstractSimulated hypobaric hypoxia (SHH) training has been used to enhance running performance. However, no studies have evaluated the effects of a single SHH exposure on healthy mice performance and analyzed the changes of mitochondria-related genes in the central nervous system. The current study used a mouse decompression chamber to simulate mild hypobaric hypoxia at the high altitude of 5000 m or severe hypobaric hypoxia at 8000 m for 16 h (SHH5000 & SHH8000, respectively). Then, the mouse behavioral tests were recorded by a modified Noldus video tracking. Third, the effects of SHH on 8 mitochondria-related genes of Drp1, Mfn1, Mfn2, Opa1, TFAM, SGK1, UCP2 and UCP4, were assessed in cerebellum, hippocampus and gastrocnemius muscles. The results have shown that a single mild or severe HH improves healthy mice performance. In cerebellum, 6 of all 8 detected genes (except Mfn2 and UCP4) did not change after SHH. In hippocampus, all detected genes did not change after SHH. In muscles, 7 of all 8 detected genes (except Opa1) did not change after SHH. The present study has indicated the benefit of a single SHH in healthy mice performance, which would due to the stabilized mitochondria against a mild stress state.

Effects of Hyperoxia on Lung Utrastructure

1970 ◽  
Vol 28 ◽  
pp. 26-27
Author(s):  
Gladys Harrison
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Light Microscopy ◽  
Oxygen Effects ◽  
Age Dependent ◽  
The Central Nervous System ◽  
The Subject ◽  
Space Age ◽  
Alveolar Septa ◽  
Extensive Damage

With the advent of the space age and the need to determine the requirements for a space cabin atmosphere, oxygen effects came into increased importance, even though these effects have been the subject of continuous research for many years. In fact, Priestly initiated oxygen research when in 1775 he published his results of isolating oxygen and described the effects of breathing it on himself and two mice, the only creatures to have had the “privilege” of breathing this “pure air”.Early studies had demonstrated the central nervous system effects at pressures above one atmosphere. Light microscopy revealed extensive damage to the lungs at one atmosphere. These changes which included perivascular and peribronchial edema, focal hemorrhage, rupture of the alveolar septa, and widespread edema, resulted in death of the animal in less than one week. The severity of the symptoms differed between species and was age dependent, with young animals being more resistant.

Emigration of neutrophils in the central nervous system

1983 ◽  
Vol 41 ◽  
pp. 788-789
Author(s):  
John L.Beggs ◽  
John D. Waggener ◽  
Wanda Miller ◽  
Jane Watkins
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Osmium Tetroxide ◽  
White Blood Cells ◽  
Arterial Perfusion ◽  
E Coli ◽  
Intracisternal Injection ◽  
The Central Nervous System ◽  
Brain And Spinal Cord ◽  
Interendothelial Junctions

Studies using mesenteric and ear chamber preparations have shown that interendothelial junctions provide the route for neutrophil emigration during inflammation. The term emigration refers to the passage of white blood cells across the endothelium from the vascular lumen. Although the precise pathway of transendo- thelial emigration in the central nervous system (CNS) has not been resolved, the presence of different physiological and morphological (tight junctions) properties of CNS endothelium may dictate alternate emigration pathways.To study neutrophil emigration in the CNS, we induced meningitis in guinea pigs by intracisternal injection of E. coli bacteria.In this model, leptomeningeal inflammation is well developed by 3 hr. After 3 1/2 hr, animals were sacrificed by arterial perfusion with 3% phosphate buffered glutaraldehyde. Tissues from brain and spinal cord were post-fixed in 1% osmium tetroxide, dehydrated in alcohols and propylene oxide, and embedded in Epon. Thin serial sections were cut with diamond knives and examined in a Philips 300 electron microscope.

Sign in / Sign up

Export Citation Format

Share Document