Difference between revisions of "Perfusion of Mouse"
From Bridges Lab Protocols
Line 4: | Line 4: | ||
*Avertin | *Avertin | ||
*Isofluorane | *Isofluorane | ||
− | *30 | + | *30 gauge needle |
*1 mL syringe | *1 mL syringe | ||
*Peristaltic pump | *Peristaltic pump | ||
Line 28: | Line 28: | ||
*Notes: | *Notes: | ||
**Avertin is light sensitive. | **Avertin is light sensitive. | ||
− | ** | + | **Degradation products are lethal. |
**Always store at 4 degree C | **Always store at 4 degree C | ||
**Do NOT use a solution that is yellow or contains a precipitate. | **Do NOT use a solution that is yellow or contains a precipitate. | ||
− | **Avertin is lipid soluble and may require a larger dose. | + | **Avertin is lipid soluble and may require a larger dose in an obese animal. |
==Perfusion Pump Set Up== | ==Perfusion Pump Set Up== | ||
− | *Place | + | *Place needle on end of tubing |
− | *Insert one tube into 9% saline solution, and one tube into 10% formalin solution | + | *Insert one tube into 0.9% saline solution, and one tube into 10% formalin solution |
''Image 1: Set up of the two tube system from 0.9% saline solution and 10% formalin solution.'' | ''Image 1: Set up of the two tube system from 0.9% saline solution and 10% formalin solution.'' | ||
[[File:perfusionbottle.png]] | [[File:perfusionbottle.png]] | ||
Line 52: | Line 52: | ||
==Animal Procedure== | ==Animal Procedure== | ||
− | *Place mouse in isofluorane chamber and | + | *Place mouse in isofluorane chamber and lightly anesthetize the animal. |
− | + | ||
*Remove mouse from chamber | *Remove mouse from chamber | ||
*For mouse anesthesia, administer 0.8 ml/20 g (of mouse body weight) Avertin through intraperitoneal injection with 30 ½ gauge needle. | *For mouse anesthesia, administer 0.8 ml/20 g (of mouse body weight) Avertin through intraperitoneal injection with 30 ½ gauge needle. | ||
Line 61: | Line 60: | ||
*Cut open the diaphragm using standard scissors. | *Cut open the diaphragm using standard scissors. | ||
**Be careful to not pierce the heart. | **Be careful to not pierce the heart. | ||
− | *Using clamp scissors, grab at the base of the | + | *Using clamp scissors, grab at the base of the sternum, cut through the ribcage and lift to expose the heart. |
*Transfer the mouse to the procedural stage/platform. | *Transfer the mouse to the procedural stage/platform. | ||
− | *Insert the 30 | + | *Insert the 30 gauge needle (from the tubing with saline/10% formalin solution) into the apex of the left ventricle, being careful to keep the tip of the needle in the lumen of the ventricle. |
− | *Immediately after inserting the needle into the left ventricle, cut the | + | *Immediately after inserting the needle into the left ventricle, cut the right ventricle using standard scissors. |
**This allows for the blood to flow out of the mouse and drain into collecting dish. | **This allows for the blood to flow out of the mouse and drain into collecting dish. | ||
*Perfuse with saline solution for 10 minutes. | *Perfuse with saline solution for 10 minutes. | ||
Line 71: | Line 70: | ||
*With the pump still on, remove needle from left ventricle. | *With the pump still on, remove needle from left ventricle. | ||
**Mouse is now fixed for tissue collection. | **Mouse is now fixed for tissue collection. | ||
− | *When collecting tissues, keep tissues in 10% formalin solution for ~24 hours | + | *When collecting tissues, keep tissues in 10% formalin solution for ~24 hours at 4 degree C. |
*Transfer tissues to PBS after for long-term storage at 4 degree C. | *Transfer tissues to PBS after for long-term storage at 4 degree C. |
Revision as of 19:14, 27 March 2015
Contents
Materials
- 0.9 % Saline solution
- 10% formalin solution
- Avertin
- Isofluorane
- 30 gauge needle
- 1 mL syringe
- Peristaltic pump
- Collecting dish
- Surgical stage/platform
- Make sure this is level with the edge of the collecting dish to allow for the need to rest during the procedure
Surgical tools:
- Dissecting scissors
- Forceps
- Clamp scissors
- Standard scissors
Avertin Preparation
- Taken from: http://web.jhu.edu/animalcare/rdf/avertin.html
- Stock Solution (1.6 g/ml)
- Mix 25 g avertin and 15.5 ml tert-amyl alcohol at room temperture for ~12 hours in a dark bottle.
- Can store stock solutions at room temperature for one year.
- Working solution (20 mg/ml)
- Mix 0.5 ml avertin stock solution and 39.5 ml 0.9% saline in dark/foil covered container.
- Filter solution through 0.2 micron filter into a dark/foiled covered container.
- Store solution at 4 degree C.
- Replace working solution each month.
- Notes:
- Avertin is light sensitive.
- Degradation products are lethal.
- Always store at 4 degree C
- Do NOT use a solution that is yellow or contains a precipitate.
- Avertin is lipid soluble and may require a larger dose in an obese animal.
Perfusion Pump Set Up
- Place needle on end of tubing
- Insert one tube into 0.9% saline solution, and one tube into 10% formalin solution
Image 1: Set up of the two tube system from 0.9% saline solution and 10% formalin solution.
- Turn pump on to a flow rate of 0.72 ml/min
- Have stopcock turned to allow for flow of saline
Image 2: Stopcock set up to allow for 0.9% saline and 10% formalin solution to flow through to main line.
- Fill line with 0.9% saline until you have a steady stream of 0.9% saline from the end of the needle.
- Turn off peristaltic pump and turn stopcock to allow for formalin solution to flow
- Turn on peristaltic pump and pump 10% formalin solution until flow fluid is before the stopcock
- Flow has not entered the main line
- Turn off peristaltic pump and turn stopcock to allow for saline to flow
- Turn on pump and pump saline through the main line at stated flow rate
Image 3: Overview of the entire perfusion setup (excluding the procedural platform in the collecting dish)
Animal Procedure
- Place mouse in isofluorane chamber and lightly anesthetize the animal.
- Remove mouse from chamber
- For mouse anesthesia, administer 0.8 ml/20 g (of mouse body weight) Avertin through intraperitoneal injection with 30 ½ gauge needle.
- Wait for 3 minutes or until the mouse no longer responds to painful stimuli, such as paw pinch before proceeding.
- Lay the mouse on its back.
- Using tweezers and operating/dissecting scissors open up the skin and expose the chest cavity.
- Cut open the diaphragm using standard scissors.
- Be careful to not pierce the heart.
- Using clamp scissors, grab at the base of the sternum, cut through the ribcage and lift to expose the heart.
- Transfer the mouse to the procedural stage/platform.
- Insert the 30 gauge needle (from the tubing with saline/10% formalin solution) into the apex of the left ventricle, being careful to keep the tip of the needle in the lumen of the ventricle.
- Immediately after inserting the needle into the left ventricle, cut the right ventricle using standard scissors.
- This allows for the blood to flow out of the mouse and drain into collecting dish.
- Perfuse with saline solution for 10 minutes.
- After 10 minutes, switch the stopcock to allow for flow of formalin solution, at same flow rate as saline.
- Perfuse for 10-12 minutes with 10% formalin solution.
- With the pump still on, remove needle from left ventricle.
- Mouse is now fixed for tissue collection.
- When collecting tissues, keep tissues in 10% formalin solution for ~24 hours at 4 degree C.
- Transfer tissues to PBS after for long-term storage at 4 degree C.