This study investigates the protective effects of Bacillus subtilis on intestinal health in heat-stressed rats. The findings demonstrate that pre-treatment with the bacteria stabilizes tight junction proteins and reduces oxidative stress, preserving intestinal structure and function.
Begin with hematoxylin and eosin-stained intestinal sections from heat-stressed rats, one orally pre-treated with buffer as a control, and the other with a Bacillus subtilis suspension.
Heat stress damages intestinal tight junction proteins, resulting in shortened villi and mucosal thinning.
Pre-treatment with the bacteria promotes the release of signaling molecules that stabilize tight junction proteins, preserving villus height and mucosal thickness.
Observe the sections under the high-resolution light microscope to identify differences in villus height.
Next, place a drop of fresh blood from each rat on glass slides and cover with coverslips.
Heat stress destabilizes erythrocyte membranes, releasing microvesicles into the bloodstream.
The bacteria reduce systemic oxidative stress, stabilizing erythrocyte membranes and minimizing vesiculation.
Observe the blood samples under the high-resolution light microscope to assess differences in vesiculation.
Preserved villus height in the intestinal section and fewer microvesicles in the blood confirm the protective effect of the bacteria under heat stress.
After preparing and staining sections of the small intestines according to the text protocol, use a high-resolution microscope to measure the intestinal villi and total mucosal thickness. Analyze at least four samples from each rat and make at least 20 measurements in each sample.
To carry out high-resolution light microscopy of blood samples, use the vibration isolation platform as a base for the microscope system with a video camera and computer to record live images. After calibrating test images according to the text protocol, place seven microliters of freshly drawn blood from each rat on a glass slide and add a coverslip. Then, photograph and record ten image frames of 72 by 53.3 micrometers squared in each sample.
Finally, using software that provides high-resolution direct-view optical images in real time, measure the concentration of vesicles.
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