Extracellular diffusion parameters in spinal cord and filum terminale of the frog
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
11070496
DOI
10.1002/1097-4547(20001115)62:4<530::aid-jnr7>3.0.co;2-7
PII: 10.1002/1097-4547(20001115)62:4<530::AID-JNR7>3.0.CO;2-7
Knihovny.cz E-zdroje
- MeSH
- cauda equina cytologie metabolismus MeSH
- difuze MeSH
- draslík metabolismus farmakologie MeSH
- edém mozku metabolismus patologie patofyziologie MeSH
- elektrická stimulace MeSH
- extracelulární prostor metabolismus MeSH
- fyziologický stres metabolismus MeSH
- gliový fibrilární kyselý protein metabolismus MeSH
- hypotonické roztoky metabolismus farmakologie MeSH
- mícha cytologie metabolismus MeSH
- neurofilamentové proteiny metabolismus MeSH
- neuroglie cytologie metabolismus MeSH
- neurony cytologie metabolismus MeSH
- počet buněk MeSH
- Rana pipiens anatomie a histologie metabolismus MeSH
- velikost buňky fyziologie MeSH
- vodní a elektrolytová rovnováha fyziologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- draslík MeSH
- gliový fibrilární kyselý protein MeSH
- hypotonické roztoky MeSH
- neurofilamentové proteiny MeSH
Extracellular space (ECS) diffusion parameters were studied in isolated frog spinal cord grey matter and filum terminale (FT), that is predominantly composed of glial cells and axons. We compared the cell swelling induced by K(+) application, hypotonic stress and tetanic stimulation of afferent input. The ECS diffusion parameters, volume fraction alpha (alpha = ECS volume/total tissue volume), tortuosity lambda (lambda(2) = free/apparent diffusion coefficient in the tissue) and non-specific cellular uptake k', were determined by the real-time iontophoretic method using TMA(+)-selective microelectrodes. Stimulation-evoked changes in extracellular K(+) concentration ([K(+)](e)) were measured by K(+)-selective microelectrodes. Histological analysis revealed that in the central region of the FT, the cell density was lower than in SC, neurons and oligodendrocytes were scarce, GFAP-positive astrocytes were abundant, and they showed thicker and more densely stained processes than in spinal cord. In the FT, alpha was 58% higher and lambda significantly lower than in the spinal cord. In 50 mM K(+), alpha in spinal cord decreased from about 0.19 to 0.09, i.e., by 53%, whereas in FT from about 0.32 to 0.20, i.e., by only 38%; lambda increased significantly more in FT than in spinal cord. Hypotonic solution (175 mmol/kg(-1)) resulted in similar decreases in alpha, and there were no changes in lambda in either spinal cord or FT. Stimulation of VIII or IX dorsal root (DR) by 30 Hz evoked an increase in [K(+)](e) from 3 to 11-12 mM in spinal cord, but to only 4-5 mM in FT. In the spinal cord this stimulation led to a 30% decrease in alpha and a small increase in lambda whereas in the FT the decrease in alpha was only about 10% and no increase in lambda was found. We conclude that in spinal cord, a complex tissue with a higher density of cellular elements than the FT, 50 mM K(+), hypotonic stress as well as DR stimulation evoked a greater decrease in ECS volume than in FT. Nevertheless, the K(+)-induced increase in tortuosity was higher in FT, suggesting that a substantial part of the K(+)-evoked increase in lambda was due to astrocytic swelling.
Citace poskytuje Crossref.org
Astrocytes and extracellular matrix in extrasynaptic volume transmission
Diffusion in brain extracellular space