Browsing by Subject "Capsaicin"
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Item The Effect of Including Capsaicin and Gut Microbiota Feed Additives on Growth Performance of Nursery Pigs(2020-12) Rosa Medina, EduardoFeed additives such as capsaicin, prebiotics, and microbiota feed additives can increase postweaning growth performance of pigs while decreasing antibiotic use. Therefore, we conducted two experiments to evaluate the growth performance of newly weaned pigs fed capsaicin, prebiotics, and microbiota feed additives. On the first experiment, we observed that feeding Capsaicin to sows during lactation and the corresponding offspring during weaning was more effective at increasing feed efficiency of weaning pigs than feeding Capsaicin only in lactation or only to nursery pigs. Likewise, there was a greater number of genes differentially expressed when sows and their offspring consumed Capsaicin than feeding to sows or nursery pigs alone. On the second experiment, we observed that the offspring of multiparous sows had greater post-weaning growth performance than those of primiparous sows and that feeding four different microbial feed additives did not increase the growth performance of the offspring of either group of sows.Item Role of the renal nerves in hypertension(2014-11) Foss, Jason DavidHigh blood pressure (hypertension; HTN) is the leading risk factor for death, yet the precise causes are unclear. The nervous system is known to play a role in some forms of HTN and research has pointed to the kidneys as a likely neural target in HTN. This possibility has been strengthened by recent clinical trials showing that ablation of the renal nerves (renal denervation; RDNX) has a significant antihypertensive effect in drug resistant patients. However, failure of the most recent sham-controlled trial has raised many questions regarding this treatment. Chief among them is whether the antihypertensive effect of RDNX is due to changes in kidney function secondary to ablation of sympathetic (efferent) renal nerves, or due to a reduction in non-renal sympathetic nerve activity secondary to ablation of sensory (afferent) renal nerves. In order to address this question, I first identified an animal model of HTN in which RDNX had an antihypertensive effect. Importantly, I showed that RDNX had roughly the same effect on blood pressure in hypertensive Dahl salt-sensitive (S) rats as has been reported in clinical trials. I then developed and validated a novel method for selective ablation of afferent renal nerves (renal-CAP treatment). Using this method, I showed that afferent renal nerves are not necessary to maintain cardiovascular or sodium/water homeostasis in normotensive rats subjected to dietary sodium loading. We also showed that renal-CAP treatment and complete RDNX caused the same attenuation of deoxycorticosterone-salt HTN, suggesting that the antihypertensive effect of RDNX in this model is due to ablation of afferent renal nerves. Lastly, we showed that RDNX has the same antihypertensive effect in Dahl S rats with mild HTN (after three weeks of high salt feeding) and in those with severe HTN (after nine weeks of high salt feeding). These results suggest that the antihypertensive effect of RDNX in the Dahl S rat is not dependent on duration of high salt feeding or pretreatment blood pressure and that the antihypertensive effect of RDNX in this model is not due to ablation of afferent renal nerves.