Home›Cell Biology›Using Zebrafish Larvae to Study the Pathological Consequences of Hemorrhagic Stroke
Cell BiologyJoVE (Open Access)Citable · DOI
Using Zebrafish Larvae to Study the Pathological Consequences of Hemorrhagic Stroke
DOI: 10.3791/59716-v
What you'll learn
✓Induce and quantify intracerebral hemorrhage in zebrafish larvae
✓Assess brain injury, neuroinflammation, and locomotor deficits post-hemorrhage
✓Apply pharmacological interventions and analyze cellular responses to stroke
Protocol
Here we present a protocol to quantify brain injury, locomotor deficits and neuroinflammation following bleeding in the brain in zebrafish larvae, in the context of human intracerebral hemorrhage (ICH).
Difficulty
advanced
Total time
~5 days (egg production through final analysis)
Model organism
Zebrafish larvae (Danio rerio)
Biosafety
BSL-1
Steps
1
Produce and collect zebrafish eggs
Set up breeding conditions and collect fertilized eggs from zebrafish pairs on Day 0. Eggs are then incubated and prepared for subsequent experimental manipulation.
▶ 00:35
2
Treat larvae with atorvastatin and induce hemorrhage
On Days 1–2, administer atorvastatin treatment to larvae and perform intracerebral hemorrhage (ICH) induction. Separate ICH-positive and ICH-negative larval populations for parallel analysis.
▶ 01:11
3
Quantify cell death, leukocytes, and motor activity
On Days 3–5, perform assays to measure brain cell death, analyze leukocyte infiltration and activation, and assess locomotor deficits using motility assays.
▶ 02:22
4
Document intracerebral hemorrhage phenotype and outcomes
Present representative results showing ICH induction success, visualization of bleeding in larval brain tissue, and quantified measurements of injury and inflammatory markers.
▶ 04:24
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