It would be helpful if you would be more specific. For example, animals might be raised stress-free but be stressed at the time of slaughter in a way that alters meat quality. Are you thinking about the entire period from birth to slaughter or some more specific period? Can you help us understand your interest more clearly?
lowering the level of glycogen in living animals and so lower the level of lactic acid in the carcass after slaughtering and so the rise the pH of the meat leading to poor shelf life of the meat( Bad Quality Meat )
stress leads to bad rigor mortis
styress leads to PSE ( Pale Soft Exudative Meat )- DFD ( Dark Firm and Dry Meat)
Here is a very good reference if you have access to the Journal of Animal Science:K. R. Buckham Sporer, P. S. D. Weber, J. L. Burton, B. Earley, M. A. Crowe. Transportation of young beef bulls alters circulating physiological parameters that may be effective biomarkers of stress. J ANIM SCI June 2008 vol. 86 no. 6 1325-1334.
thanks for the great reference Prof Jack Haiden Britt. its now clear that cortisol assay is one of the key parameters to look in measure of effects of stress at transportation.
interestingly plasma BHBA remains within constant range (Buckham et al..2008)
One of the problems, whatever you choose as a marker, is in establishing concentrations in "zero" or "start" stress conditions. To look at this I would sample a quarter of the animals at zero time, half at some time later (after transit ?) , three quarters at a later time and all of them on the final occasion. The animals in the first quarter would be naïve in terms of blood sampling at zero time, have experienced blood sampling once before at the second etc - you can look at the effect of experience of blood sampling on the variable you have chosen. You should remember that blood concentrations of all the variables suggested for use are influenced by stress, so you should look at the effects of order of sampling within a group of animals and the time taken to get a blood sample on concentrations. With sheep, we would exclude samples that had taken us longer to start collecting than 20 seconds from entering a pen of sheep. We used cortisol, glucose, lactate AND electrolytes - Ca, Mg, Na, & K