Did you know ?

General anesthetics can introduce bias by disturbing the physiology and affecting signal expression, so affecting directly the pathology of an animal model.

With the In Actio Module of the PhotonIMAGER, you can avoid these side effects and improve your results

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IN ACTIO MODULE
Imaging of freely moving animals


The In Actio Module of the PhotonIMAGER™ makes it possible to image non-anesthetized, freely moving animals and opens previously unimagined new avenues for research.

A video monitoring function to track the animal during acquisition



The patented In Actio imaging principle adds a video acquisition to your optical imaging experiments. The video is done by illuminating the animal with an infrared laser. The signal coming from the animal is the combination of the infrared lighting and your biological signal, which is split by a dichronic beamsplitter. The localization lighting is then only recorded by a dedicated CCD camera as the intensified CCD camera continues to acquire, as usual, the biological signal. Acquisitions are done at 45 frames per second.

Dynamic imaging for dynamic biological phenomena

Conventional optical imaging instruments are often limited to acquiring still images and only offer quantification of signal which reveals the expression of a molecule at fixed moment in time. Yet biological phenomena are always dynamic, and so a single observation at a fixed time point more often than not results in an incomplete view of the overall process, which results in misinterpretation of the available data. Such ’Snap-shot”-like observation results in the loss of information on fast moving dynamic phenomena. Conventional non invasive optical in vivo molecular imaging modalities also have the following limitations:

- Animals are required to be stationary which necessitates the use of anesthesia. Anesthesia is a time consuming step and reduces the throughput of an imaging system.
- Anesthesia can introduce bias by disturbing the physiology and affecting signal expression, so affecting directly the pathology of an animal model. (cf Anesthesia and other considerations for in vivo imaging of small animals, Hildebrandt et al, ILAR 2008).
- Imaging an animal in motion is not possible, so monitoring calcium activity in the brain during sleep and wake cycles or observing a bioluminescent signal in a contracting muscle non invasively in vivo is not possible.

No Anesthesia recquired for your acquisitions

The In Actio module makes it possible to image non anesthetized, freely moving animals and opens previously unimagined new avenues for research . The In Actio module simultaneously records both bioluminescence signal and a bright field video of the animal under infra red illumination for co-registration; thereby extending the the imaging capabilities of the Photon Imager from recording dynamic signal from an anesthetized animal, to recording dynamic signal from a free moving animal. The In Actio module offers the following advantages in circumstances where there is no need for multiple views of the animal, as provided by the 3D Module:

Improved physiological relevance
observe physiological or pathological phenomena free from any perturbation by anesthesia.

Reduce the time for animal preparation
Anesthesia is no longer required and animal stress is reduced.

Higher throughput
Without anesthesia the experimental procedure is made faster and several animals can be imaged simultaneously.

In Actio Imaging Applications

Molecular approaches to behavioral sudies, i.e.: Calcium flux during sleep and wake cycles

Functional physiological studies, i.e.: Calcium imaging during muscular contraction

Subcutaneous tumor monitoring in awake animals

Fish with persistent luminescence nanoparticules:

 


Freely moving mouse with subcutaneous luminescent nanoparticules (imaged with a temporal resolution of 20 ms):




Micondrial calcium uptake during striated muscle contraction
BRET imaging with a Aequorin-GFP genetic reporter targetted to the mito-
chondrial matrix.


Rogers KL, et al (2007). PLoSONE 2(10): e974. doi:10.1371/journal.pone.0000974


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