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Apparatus for long-term ventricular access in the awake canine
Journal of Applied Physiology (Bethesda, Md. : 1985)
|July 1, 1986
Summary
This study introduces a novel apparatus for cerebrospinal fluid (CSF) sampling and infusion in awake dogs. The device enables repeated ventricular cannulation, facilitating central nervous system research.
Area of Science:
- Neuroscience
- Surgical Innovation
Background:
- Cerebrospinal fluid (CSF) research is crucial for understanding central nervous system (CNS) function.
- Previous methods for CSF sampling and infusion in awake animals were limited.
- The need for a reliable apparatus for repeated ventricular access in conscious canines was identified.
Purpose of the Study:
- To describe and evaluate a new apparatus for lateral ventricular cerebrospinal fluid (CSF) sampling and infusion in awake dogs.
- To assess the safety and efficacy of the apparatus for repeated experimental procedures.
- To investigate the central nervous system effects of peptide administration via the apparatus.
Main Methods:
- Development and application of a novel apparatus for ventricular cannulation in awake canines.
- Repeated CSF sampling and intracerebroventricular infusions of peptides (bombesin, somatostatin) over a 6- to 24-month period.
- Monitoring of CSF and peripheral blood peptide levels using radioimmunoassay.
Main Results:
- The apparatus allowed for safe and repeated CSF sampling and intracerebroventricular infusions in 25 dogs.
- Intracerebroventricular peptide administration resulted in detectable levels in CSF but not in peripheral blood, suggesting limited systemic leakage.
- Complications occurred in 10 dogs but were manageable, with three fatal outcomes (meningitis, seizures).
Conclusions:
- The described apparatus provides a viable method for repeated ventricular cannulation in awake canines.
- This tool facilitates the study of CSF dynamics and the central effects of administered substances.
- The findings support the use of this apparatus for CNS research without significant systemic peptide absorption.