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Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study.
Magnetic resonance spectroscopy was used to study intracellular pH and compounds which contain phosphorus in normal human brain and primary brain tumours non-invasively. In normal subjects (n = 7) intracellular pH (pHi) of the brain was 7.03 +/- 0.02 (mean +/- s.e.m.). The pHi did not vary between s...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1989
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2247178/ https://www.ncbi.nlm.nih.gov/pubmed/2551360 |
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author | Cadoux-Hudson, T. A. Blackledge, M. J. Rajagopalan, B. Taylor, D. J. Radda, G. K. |
author_facet | Cadoux-Hudson, T. A. Blackledge, M. J. Rajagopalan, B. Taylor, D. J. Radda, G. K. |
author_sort | Cadoux-Hudson, T. A. |
collection | PubMed |
description | Magnetic resonance spectroscopy was used to study intracellular pH and compounds which contain phosphorus in normal human brain and primary brain tumours non-invasively. In normal subjects (n = 7) intracellular pH (pHi) of the brain was 7.03 +/- 0.02 (mean +/- s.e.m.). The pHi did not vary between superficial (2 cm, majority grey matter) and deep brain (5 cm, majority white matter). The relative concentrations of phosphocreatine (PCr) and phosphomonoesters (PME) to ATP were also constant with depth. The relative concentration of phosphodiesters (PDE) increased from superficial to deep in normal brain. The astrocytomas (n = 7, grade II-IV) were significantly more alkaline (pHi = 7.08 +/- 0.03), and contained more PCr and PME, with respect to ATP, than normal brain at similar depth. The meningiomas (n = 4) were also more alkaline (pHi = 7.19 +/- 0.02) with a raised PME level but reduced PCr. The reduction in meningioma PCr may be due to the significant necrosis (greater than 20%) seen in the surgical biopsies. No significant necrosis was seen in the gliomas. Previous in vitro studies suggest that increased PME may be due to accumulation of phosphoethanolamine (PE), a phospholipid precursor. These results suggest that human primary brain tumours characteristically are more alkaline with increased PME than normal brain. IMAGES: |
format | Text |
id | pubmed-2247178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22471782009-09-10 Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. Cadoux-Hudson, T. A. Blackledge, M. J. Rajagopalan, B. Taylor, D. J. Radda, G. K. Br J Cancer Research Article Magnetic resonance spectroscopy was used to study intracellular pH and compounds which contain phosphorus in normal human brain and primary brain tumours non-invasively. In normal subjects (n = 7) intracellular pH (pHi) of the brain was 7.03 +/- 0.02 (mean +/- s.e.m.). The pHi did not vary between superficial (2 cm, majority grey matter) and deep brain (5 cm, majority white matter). The relative concentrations of phosphocreatine (PCr) and phosphomonoesters (PME) to ATP were also constant with depth. The relative concentration of phosphodiesters (PDE) increased from superficial to deep in normal brain. The astrocytomas (n = 7, grade II-IV) were significantly more alkaline (pHi = 7.08 +/- 0.03), and contained more PCr and PME, with respect to ATP, than normal brain at similar depth. The meningiomas (n = 4) were also more alkaline (pHi = 7.19 +/- 0.02) with a raised PME level but reduced PCr. The reduction in meningioma PCr may be due to the significant necrosis (greater than 20%) seen in the surgical biopsies. No significant necrosis was seen in the gliomas. Previous in vitro studies suggest that increased PME may be due to accumulation of phosphoethanolamine (PE), a phospholipid precursor. These results suggest that human primary brain tumours characteristically are more alkaline with increased PME than normal brain. IMAGES: Nature Publishing Group 1989-09 /pmc/articles/PMC2247178/ /pubmed/2551360 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Cadoux-Hudson, T. A. Blackledge, M. J. Rajagopalan, B. Taylor, D. J. Radda, G. K. Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
title | Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
title_full | Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
title_fullStr | Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
title_full_unstemmed | Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
title_short | Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
title_sort | human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2247178/ https://www.ncbi.nlm.nih.gov/pubmed/2551360 |
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