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Cerebrospinal fluid is drained primarily via the spinal canal and olfactory route in young and aged spontaneously hypertensive rats
Many aspects of CSF dynamics are poorly understood due to the difficulties involved in quantification and visualization. In particular, there is debate surrounding the route of CSF drainage. Our aim was to quantify CSF flow, volume, and drainage route dynamics in vivo in young and aged spontaneously...
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Published in: | Fluids and barriers of the CNS 2014-06, Vol.11 (1), p.12-12, Article 12 |
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description | Many aspects of CSF dynamics are poorly understood due to the difficulties involved in quantification and visualization. In particular, there is debate surrounding the route of CSF drainage. Our aim was to quantify CSF flow, volume, and drainage route dynamics in vivo in young and aged spontaneously hypertensive rats (SHR) using a novel contrast-enhanced computed tomography (CT) method.
ICP was recorded in young (2-5 months) and aged (16 months) SHR. Contrast was administered into the lateral ventricles bilaterally and sequential CT imaging was used to visualize the entire intracranial CSF system and CSF drainage routes. A customized contrast decay software module was used to quantify CSF flow at multiple locations.
ICP was significantly higher in aged rats than in young rats (11.52 ± 2.36 mmHg, versus 7.04 ± 2.89 mmHg, p = 0.03). Contrast was observed throughout the entire intracranial CSF system and was seen to enter the spinal canal and cross the cribriform plate into the olfactory mucosa within 9.1 ± 6.1 and 22.2 ± 7.1 minutes, respectively. No contrast was observed adjacent to the sagittal sinus. There were no significant differences between young and aged rats in either contrast distribution times or CSF flow rates. Mean flow rates (combined young and aged) were 3.0 ± 1.5 μL/min at the cerebral aqueduct; 3.5 ± 1.4 μL/min at the 3rd ventricle; and 2.8 ± 0.9 μL/min at the 4th ventricle. Intracranial CSF volumes (and as percentage total brain volume) were 204 ± 97 μL (8.8 ± 4.3%) in the young and 275 ± 35 μL (10.8 ± 1.9%) in the aged animals (NS).
We have demonstrated a contrast-enhanced CT technique for measuring and visualising CSF dynamics in vivo. These results indicate substantial drainage of CSF via spinal and olfactory routes, but there was little evidence of drainage via sagittal sinus arachnoid granulations in either young or aged animals. The data suggests that spinal and olfactory routes are the primary routes of CSF drainage and that sagittal sinus arachnoid granulations play a minor role, even in aged rats with higher ICP. |
doi_str_mv | 10.1186/2045-8118-11-12 |
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ICP was recorded in young (2-5 months) and aged (16 months) SHR. Contrast was administered into the lateral ventricles bilaterally and sequential CT imaging was used to visualize the entire intracranial CSF system and CSF drainage routes. A customized contrast decay software module was used to quantify CSF flow at multiple locations.
ICP was significantly higher in aged rats than in young rats (11.52 ± 2.36 mmHg, versus 7.04 ± 2.89 mmHg, p = 0.03). Contrast was observed throughout the entire intracranial CSF system and was seen to enter the spinal canal and cross the cribriform plate into the olfactory mucosa within 9.1 ± 6.1 and 22.2 ± 7.1 minutes, respectively. No contrast was observed adjacent to the sagittal sinus. There were no significant differences between young and aged rats in either contrast distribution times or CSF flow rates. Mean flow rates (combined young and aged) were 3.0 ± 1.5 μL/min at the cerebral aqueduct; 3.5 ± 1.4 μL/min at the 3rd ventricle; and 2.8 ± 0.9 μL/min at the 4th ventricle. Intracranial CSF volumes (and as percentage total brain volume) were 204 ± 97 μL (8.8 ± 4.3%) in the young and 275 ± 35 μL (10.8 ± 1.9%) in the aged animals (NS).
We have demonstrated a contrast-enhanced CT technique for measuring and visualising CSF dynamics in vivo. These results indicate substantial drainage of CSF via spinal and olfactory routes, but there was little evidence of drainage via sagittal sinus arachnoid granulations in either young or aged animals. The data suggests that spinal and olfactory routes are the primary routes of CSF drainage and that sagittal sinus arachnoid granulations play a minor role, even in aged rats with higher ICP.</description><identifier>ISSN: 2045-8118</identifier><identifier>EISSN: 2045-8118</identifier><identifier>DOI: 10.1186/2045-8118-11-12</identifier><identifier>PMID: 24932405</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Brain research ; Catheters ; Colleges & universities ; CT imaging ; Hospitals ; Hypertension ; Measurement ; Medical imaging ; Methods ; Neurology ; Physiological aspects ; Rodents ; Tomography</subject><ispartof>Fluids and barriers of the CNS, 2014-06, Vol.11 (1), p.12-12, Article 12</ispartof><rights>COPYRIGHT 2014 BioMed Central Ltd.</rights><rights>2014 Murtha et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.</rights><rights>Copyright © 2014 Murtha et al.; licensee BioMed Central Ltd. 2014 Murtha et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b677t-81fdefe1979c0b04b68981709a9d677fdd5702b2f3699eaf2dd672e9dfa70f3b3</citedby><cites>FETCH-LOGICAL-b677t-81fdefe1979c0b04b68981709a9d677fdd5702b2f3699eaf2dd672e9dfa70f3b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057524/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1538645955?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25730,27900,27901,36988,36989,44565,53765,53767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24932405$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murtha, Lucy A</creatorcontrib><creatorcontrib>Yang, Qing</creatorcontrib><creatorcontrib>Parsons, Mark W</creatorcontrib><creatorcontrib>Levi, Christopher R</creatorcontrib><creatorcontrib>Beard, Daniel J</creatorcontrib><creatorcontrib>Spratt, Neil J</creatorcontrib><creatorcontrib>McLeod, Damian D</creatorcontrib><title>Cerebrospinal fluid is drained primarily via the spinal canal and olfactory route in young and aged spontaneously hypertensive rats</title><title>Fluids and barriers of the CNS</title><addtitle>Fluids Barriers CNS</addtitle><description>Many aspects of CSF dynamics are poorly understood due to the difficulties involved in quantification and visualization. In particular, there is debate surrounding the route of CSF drainage. Our aim was to quantify CSF flow, volume, and drainage route dynamics in vivo in young and aged spontaneously hypertensive rats (SHR) using a novel contrast-enhanced computed tomography (CT) method.
ICP was recorded in young (2-5 months) and aged (16 months) SHR. Contrast was administered into the lateral ventricles bilaterally and sequential CT imaging was used to visualize the entire intracranial CSF system and CSF drainage routes. A customized contrast decay software module was used to quantify CSF flow at multiple locations.
ICP was significantly higher in aged rats than in young rats (11.52 ± 2.36 mmHg, versus 7.04 ± 2.89 mmHg, p = 0.03). Contrast was observed throughout the entire intracranial CSF system and was seen to enter the spinal canal and cross the cribriform plate into the olfactory mucosa within 9.1 ± 6.1 and 22.2 ± 7.1 minutes, respectively. No contrast was observed adjacent to the sagittal sinus. There were no significant differences between young and aged rats in either contrast distribution times or CSF flow rates. Mean flow rates (combined young and aged) were 3.0 ± 1.5 μL/min at the cerebral aqueduct; 3.5 ± 1.4 μL/min at the 3rd ventricle; and 2.8 ± 0.9 μL/min at the 4th ventricle. Intracranial CSF volumes (and as percentage total brain volume) were 204 ± 97 μL (8.8 ± 4.3%) in the young and 275 ± 35 μL (10.8 ± 1.9%) in the aged animals (NS).
We have demonstrated a contrast-enhanced CT technique for measuring and visualising CSF dynamics in vivo. These results indicate substantial drainage of CSF via spinal and olfactory routes, but there was little evidence of drainage via sagittal sinus arachnoid granulations in either young or aged animals. The data suggests that spinal and olfactory routes are the primary routes of CSF drainage and that sagittal sinus arachnoid granulations play a minor role, even in aged rats with higher ICP.</description><subject>Brain research</subject><subject>Catheters</subject><subject>Colleges & universities</subject><subject>CT imaging</subject><subject>Hospitals</subject><subject>Hypertension</subject><subject>Measurement</subject><subject>Medical imaging</subject><subject>Methods</subject><subject>Neurology</subject><subject>Physiological aspects</subject><subject>Rodents</subject><subject>Tomography</subject><issn>2045-8118</issn><issn>2045-8118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNks9rFDEUxwdRbKk9e5OAIF62TTKZzOQi1EWrUPCi55CZvOymZJM1ySzs2X_cTHe77koFE0ge733yJe9HVb0m-IqQjl9TzJpZV8wZITNCn1XnB8_zI_usukzpHpfFWIs5fVmdUSZqynBzXv2aQ4Q-hrS2Xjlk3Gg1sgnpqKwHjdbRrlS0bos2VqG8BLQnBzWdymsUnFFDDnGLYhgzIOvRNox-8RBUiyKS1sFn5SGMqQgtt2uIGXyyG0BR5fSqemGUS3C5vy-qH58_fZ9_md19u_06v7mb9bxtc8nFaDBARCsG3GPW8050pMVCCV0Ao3XTYtpTU3MhQBmqi5uC0Ea12NR9fVF92Omux34FegCfo3Jyl-JWBmXlacTbpVyEjSyVahvKisDHnUBvwz8ETiNDWMmpD3LqgyREElpE3u9_EcPPEVKWK5sGcG5XIEkahinldYf_A6057xhnvKBv_0LvwxhLix6ojrNGNM0faqEcSOtNKN8cJlF509SCd3UrukJdPUGVrWFlh-DB2OI_efDu6MESlMvLFNyYbfDpFLzegUOZuBTBHGpHsJxm-olqvTnu2YF_nOD6N5No8og</recordid><startdate>20140606</startdate><enddate>20140606</enddate><creator>Murtha, Lucy A</creator><creator>Yang, Qing</creator><creator>Parsons, Mark W</creator><creator>Levi, Christopher R</creator><creator>Beard, Daniel J</creator><creator>Spratt, Neil J</creator><creator>McLeod, Damian D</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140606</creationdate><title>Cerebrospinal fluid is drained primarily via the spinal canal and olfactory route in young and aged spontaneously hypertensive rats</title><author>Murtha, Lucy A ; Yang, Qing ; Parsons, Mark W ; Levi, Christopher R ; Beard, Daniel J ; Spratt, Neil J ; McLeod, Damian D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b677t-81fdefe1979c0b04b68981709a9d677fdd5702b2f3699eaf2dd672e9dfa70f3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Brain research</topic><topic>Catheters</topic><topic>Colleges & universities</topic><topic>CT imaging</topic><topic>Hospitals</topic><topic>Hypertension</topic><topic>Measurement</topic><topic>Medical imaging</topic><topic>Methods</topic><topic>Neurology</topic><topic>Physiological aspects</topic><topic>Rodents</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murtha, Lucy A</creatorcontrib><creatorcontrib>Yang, Qing</creatorcontrib><creatorcontrib>Parsons, Mark W</creatorcontrib><creatorcontrib>Levi, Christopher R</creatorcontrib><creatorcontrib>Beard, Daniel J</creatorcontrib><creatorcontrib>Spratt, Neil J</creatorcontrib><creatorcontrib>McLeod, Damian D</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Fluids and barriers of the CNS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murtha, Lucy A</au><au>Yang, Qing</au><au>Parsons, Mark W</au><au>Levi, Christopher R</au><au>Beard, Daniel J</au><au>Spratt, Neil J</au><au>McLeod, Damian D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebrospinal fluid is drained primarily via the spinal canal and olfactory route in young and aged spontaneously hypertensive rats</atitle><jtitle>Fluids and barriers of the CNS</jtitle><addtitle>Fluids Barriers CNS</addtitle><date>2014-06-06</date><risdate>2014</risdate><volume>11</volume><issue>1</issue><spage>12</spage><epage>12</epage><pages>12-12</pages><artnum>12</artnum><issn>2045-8118</issn><eissn>2045-8118</eissn><abstract>Many aspects of CSF dynamics are poorly understood due to the difficulties involved in quantification and visualization. In particular, there is debate surrounding the route of CSF drainage. Our aim was to quantify CSF flow, volume, and drainage route dynamics in vivo in young and aged spontaneously hypertensive rats (SHR) using a novel contrast-enhanced computed tomography (CT) method.
ICP was recorded in young (2-5 months) and aged (16 months) SHR. Contrast was administered into the lateral ventricles bilaterally and sequential CT imaging was used to visualize the entire intracranial CSF system and CSF drainage routes. A customized contrast decay software module was used to quantify CSF flow at multiple locations.
ICP was significantly higher in aged rats than in young rats (11.52 ± 2.36 mmHg, versus 7.04 ± 2.89 mmHg, p = 0.03). Contrast was observed throughout the entire intracranial CSF system and was seen to enter the spinal canal and cross the cribriform plate into the olfactory mucosa within 9.1 ± 6.1 and 22.2 ± 7.1 minutes, respectively. No contrast was observed adjacent to the sagittal sinus. There were no significant differences between young and aged rats in either contrast distribution times or CSF flow rates. Mean flow rates (combined young and aged) were 3.0 ± 1.5 μL/min at the cerebral aqueduct; 3.5 ± 1.4 μL/min at the 3rd ventricle; and 2.8 ± 0.9 μL/min at the 4th ventricle. Intracranial CSF volumes (and as percentage total brain volume) were 204 ± 97 μL (8.8 ± 4.3%) in the young and 275 ± 35 μL (10.8 ± 1.9%) in the aged animals (NS).
We have demonstrated a contrast-enhanced CT technique for measuring and visualising CSF dynamics in vivo. These results indicate substantial drainage of CSF via spinal and olfactory routes, but there was little evidence of drainage via sagittal sinus arachnoid granulations in either young or aged animals. The data suggests that spinal and olfactory routes are the primary routes of CSF drainage and that sagittal sinus arachnoid granulations play a minor role, even in aged rats with higher ICP.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24932405</pmid><doi>10.1186/2045-8118-11-12</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Brain research Catheters Colleges & universities CT imaging Hospitals Hypertension Measurement Medical imaging Methods Neurology Physiological aspects Rodents Tomography |
title | Cerebrospinal fluid is drained primarily via the spinal canal and olfactory route in young and aged spontaneously hypertensive rats |
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