Application of motion history image (MHI) on dynamic fluorescent imaging for monitoring cerebral ischemia induced by occlusion of middle cerebral artery (MCA) in mouse brain

2.1.Theory

The MHI is a view-based temporal template method [13–15]. It has been applied successfully to various LSCI data to visualize the perfusion variation locations during different stimuli [9,10]. It generates a single bidimensional map from an image sequence showing perfusion variations in time. In the generated image, each pixel is a function of recency of motion (perfusion variations in our case) of the image sequence.

MHI detects the motion of an object based on the time stamps of pixels over a set of images corresponding to a motion sequence. MHI computes a single static and bidimensional map that integrates both the spatial location as well as the temporal history of motion in the object and thus the spatial and temporal resolutions gets retained. The bidimensional MHI image can be constructed according to the algorithm that each pixel in the MHI is labeled with the timestamp (hour, minute, second, and millisecond etc.) and will be dropped out if it does not present significant change following a certain time lapse, known as the lifetime of the MHI. In the MHI, the most recent movement appears as bright in the gray scale.

The MHI Hτk(i,j) can be computed as per the following equation [13,16]

Figure 1(a) shows an example of random movement of cursor at different time points on a computer screen. The corresponding MHI image presented in Fig. 1(b) clearly shows all the spatial as well as temporal movements of the cursor. The most recent movement is shown by red color while the initial motion by blue color. Thus a bidimentional image reflecting the motion with time can be generated using MHI.

Fig. 1.

(a) Movement of cursor on a computer screen at different time points of event. (b) MHI image generated by computing threshold image of the difference of images shown in Fig. 1(a). The MHI clearly shows the movements of the cursor at different time points. As can be seen the most recent motion is highlighted by red color while the initial cursor position during its motion is represented by blue color.

Fig. 2.

The DF images (Copyright Scientific Reports, Springer Nature, Reproduced with permission) showing effect of occlusion of the middle cerebral artery (MCA) in the right hemisphere of a mouse brain [1]. The color bar for the corresponding images is indicated in ref. [1].

2.2.Materials

We demonstrate the application of the MHI algorithm on DF data recorded during occlusion of the middle cerebral artery (MCAO) in a mouse [1]. The data consists of a real-time video sequence of DF images during occlusion of the middle cerebral artery (MCAO) in a mouse. The acute cerebral ischemic event was produced by occlusion of the middle cerebral artery (MCA) [1].

The images show cortical blood flow following occlusion of the middle cerebral artery (MCAO) [1]. The video footage was acquired during a 20 seconds interval after the fluorescein administration into the tail vein and details of the experiment and image acquisition procedure can be studied in reference [1].

3.1.Monitoring perfusion variation during an induced occlusion of the middle cerebral artery (MCA) of a mouse brain

Figure 2 presents typical frames sequence of DF images recorded during an acute cerebral ischemic event where the effect of occlusion on the perfusion in the right hemisphere can be seen. The sequence rather shows the kinetics of blood flow and blood vessels appear as brighter areas [1]. The blood perfusion variation can be followed at different time points of the event. An acute cerebral ischemic event was induced by occlusion of the middle cerebral artery (MCA) of mice [1]. Each image corresponds to the time after the occlusion.

Fig. 3.

The MHIs showing clearly the areas with low perfusion in the right hemisphere of a mouse brain during induced occlusion of the middle cerebral artery (MCA). Each MHI was generated from a stack of DF images around a particular time point given in Fig. 2. For the computation of each MHI, a buffer of 8 images with a threshold value of 14 was used.

Fig. 4.

MHI images computed with different threshold values and with a buffer size of 8. The threshold value is equal to (a) 6; (b) 14; (c) 24; (d) 34.

Fig. 5.

MHI images generated with different buffer sizes with a threshold value of 14. The buffer size is equal to (a) 4; (b) 6; (c) 8; (d) 10.

To visualize the cerebral blood flow changes during occlusion, MHI method was implemented on the corresponding DF images [1]. Figure 3 shows the corresponding MHI images at different time points of event. Each MHI was computed from DF images around the frames shown in Fig. 2. The MHIs clearly illustrates the locations where perfusion decreases during occlusion. This was found more pronounced than in the raw DF images shown. The colors in the corresponding MHIs can be used to indicate perfusion evolution with time and since the sampling frequency of the data is known, a quantitative relationship between colorbar (pixel values) and the time points could be obtained [9,10].

For the computation of each MHI map, we used a buffer of 8 images with a threshold value of 14 over a stack of images shown in Fig. 2.

In the MHI, proper adjustment of its parameters values such as the level of threshold and the buffer size enhances the quality of images [9,10].

3.2.Effect of threshold values and buffer size on the MHI map

Figure 4 shows the effect of threshold values on the resulting MHI image. It shows MHI images generated with different threshold values and a buffer size of 8. From the Fig. 4 one can observe that the adjustment of threshold value reinforces the ability to distinguish distinct areas of activity (here perfusion areas).

Figure 5 shows the MHI images generated with different buffer size and a threshold value of 14. From the Fig. 5 we observe that the buffer size determines the ability to get information linked with lower activities (here low perfusion value during occlusion).