4.4 Article

A step-by-step guide for microsurgical collection of uncontaminated cerebrospinal fluid from rat cisterna magna

期刊

JOURNAL OF NEUROSCIENCE METHODS
卷 352, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jneumeth.2021.109085

关键词

Cerebrospinal fluid; CSF sampling; Cisterna magna; Rat; Microsurgical technique; Central nervous system; brain-immune communication pathways

资金

  1. Internal Research Funding (IFORES) of the University Hospital Essen [D/107-41030]
  2. University Medicine Essen Clinician Scientist Academy
  3. Deutsche Forschungsgemeinschaft (DFG
  4. German Research Foundation) [D/107-21930]
  5. DFG [SFB1280, TP A18, 316803389]

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The study introduced a microsurgical technique for collecting large quantities of uncontaminated CSF from rats, which is easy to perform without special surgical skills and can result in multiple high volume CSF collections in a short surgical time.
Background: Cerebrospinal fluid (CSF) analysis is of significant clinical importance for the diagnosis of diseases. In humans, CSF is easily accessible and can be collected using minimally invasive methods. However, obtaining uncontaminated CSF from rats is still challenging. New Method: This study described a microsurgical technique for sampling large quantities (>200 ILL) of clear and non-blood-contaminated CSF from the rat cisterna magna in a comprehensible step-by-step guide and provided a graphical visualization. Results: CSF was sampled in 5-10 min (n = 29 animals; average surgical time 7.6 min). In visual control, 28 samples (97 %) of clear and uncontaminated CSF were obtained. The volume of CSF collected was 124-337 ILL, with an average volume of 207 ILL/sample. Using the Valsalva maneuver, we could collect higher volumes (up to 400 ILL) several times. Comparison with Existing Method(s): There is no need for special surgical skills to perform this method accurately. The method takes a few minutes longer than a percutaneous puncture (<1 min in pups). However, the volume of CSF obtained using the percutaneous approach in adult rats (50-70 ILL) is comparatively low. Conclusions: We described a practical method of sampling CSF from rats that enables large volumes of CSF to be collected without blood contamination. No special surgical skills are required to use this method. With proper practice, the time between skin incision and CSF sampling is <10 min. Depending on the experimental design requirements, some additional time must be planned for wound closure.

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