Therapeutic hypothermia (TH) has demonstrated neuroprotection in instances of cardiac arrest and neonatal hypoxia/ischemia but faces different challenges in application to stroke due to the activation of cold defense mechanisms in conscious patients. This dissertation examines the efficacy and specificity of capsinoids (a purified mixture of capsiate and dihydrocapsiate) to induce a sustained mild hypothermia in conscious mice that is neuroprotective after stroke. Capsinoids function as TRPV1 agonists. However, unlike capsaicin, capsinoids are vulnerable to esterase-mediated breakdown, thus significantly restricting their action to the site of delivery. We showed that capsinoids delivered intraperitoneally (IP) to mice induced a TRPV1-dependent drop in core body temperature into the mild hypothermia range (32-34 °C). Core temperatures dropped without triggering observable cold defense mechanisms (e.g. shivering). The response to capsinoids was dose-dependent and effective in young and aged mice of both sexes. Repeated administration of capsinoids maintained mild hypothermia for up to 6 hours, supporting the potential for applying this cooling procedure for promoting post-stroke TH. Capsinoid-induced hypothermia was linked to an activation of heat defense mechanisms, as evidenced by the rapid induction of cutaneous vasodilation and subsequent drop in core body temperature. We showed that IP capsinoids activate vagal afferents, as demonstrated by an increase in c-Fos positive neurons in the nodose ganglion. Finally, we provide evidence that capsinoid-induced hypothermia is neuroprotective after ischemic stroke and significantly improves short- and long-term outcomes.
","abstract_html":"<p>Therapeutic hypothermia (TH) has demonstrated neuroprotection in instances of cardiac arrest and neonatal hypoxia/ischemia but faces different challenges in application to stroke due to the activation of cold defense mechanisms in conscious patients. This dissertation examines the efficacy and specificity of capsinoids (a purified mixture of capsiate and dihydrocapsiate) to induce a sustained mild hypothermia in conscious mice that is neuroprotective after stroke. Capsinoids function as TRPV1 agonists. However, unlike capsaicin, capsinoids are vulnerable to esterase-mediated breakdown, thus significantly restricting their action to the site of delivery. We showed that capsinoids delivered intraperitoneally (IP) to mice induced a TRPV1-dependent drop in core body temperature into the mild hypothermia range (32-34 °C). Core temperatures dropped without triggering observable cold defense mechanisms (e.g. shivering). The response to capsinoids was dose-dependent and effective in young and aged mice of both sexes. Repeated administration of capsinoids maintained mild hypothermia for up to 6 hours, supporting the potential for applying this cooling procedure for promoting post-stroke TH. Capsinoid-induced hypothermia was linked to an activation of heat defense mechanisms, as evidenced by the rapid induction of cutaneous vasodilation and subsequent drop in core body temperature. We showed that IP capsinoids activate vagal afferents, as demonstrated by an increase in c-Fos positive neurons in the nodose ganglion. Finally, we provide evidence that capsinoid-induced hypothermia is neuroprotective after ischemic stroke and significantly improves short- and long-term outcomes.</p>","abstract_has_math":false,"creators":["Andersohn, Alexander",""],"institution":null,"degree_name":"Doctor of Philosophy (PhD)","degree_level":"Dissertation (PhD)","degree_discipline":null,"degree_department":null,"school":null,"contributors":["Sean Marrelli, PhD","Louise D McCullough, MD, PhD","Harry Karmouty-Quintana, PhD"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2025,"date_issued":"2025-12-01T08:00:00Z","date_published":"2025-12-01T08:00:00Z","updated_at":"2026-07-24T05:50:47Z","subjects":["TRPV1","Capsinoid","Capsiate","Ischemic Stroke","Therapeutic Hypothermia","Molecular and Cellular Neuroscience","Neurosciences"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1493","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Sean Marrelli, PhD","Louise D McCullough, MD, PhD","Harry Karmouty-Quintana, PhD"]},{"key":"dc:creator","label":"Author","values":["Andersohn, Alexander",""]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2025-12-04T08:00:00Z"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation (PhD)"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy (PhD)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["TRPV1","Capsinoid","Capsiate","Ischemic Stroke","Therapeutic Hypothermia","Molecular and Cellular Neuroscience","Neurosciences"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1493"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Therapeutic hypothermia (TH) has demonstrated neuroprotection in instances of cardiac arrest and neonatal hypoxia/ischemia but faces different challenges in application to stroke due to the activation of cold defense mechanisms in conscious patients. This dissertation examines the efficacy and specificity of capsinoids (a purified mixture of capsiate and dihydrocapsiate) to induce a sustained mild hypothermia in conscious mice that is neuroprotective after stroke. Capsinoids function as TRPV1 agonists. However, unlike capsaicin, capsinoids are vulnerable to esterase-mediated breakdown, thus significantly restricting their action to the site of delivery. We showed that capsinoids delivered intraperitoneally (IP) to mice induced a TRPV1-dependent drop in core body temperature into the mild hypothermia range (32-34 °C). Core temperatures dropped without triggering observable cold defense mechanisms (e.g. shivering). The response to capsinoids was dose-dependent and effective in young and aged mice of both sexes. Repeated administration of capsinoids maintained mild hypothermia for up to 6 hours, supporting the potential for applying this cooling procedure for promoting post-stroke TH. Capsinoid-induced hypothermia was linked to an activation of heat defense mechanisms, as evidenced by the rapid induction of cutaneous vasodilation and subsequent drop in core body temperature. We showed that IP capsinoids activate vagal afferents, as demonstrated by an increase in c-Fos positive neurons in the nodose ganglion. Finally, we provide evidence that capsinoid-induced hypothermia is neuroprotective after ischemic stroke and significantly improves short- and long-term outcomes.
"]},{"key":"dc:title","label":"Title","values":["Capsinoids, Non-Pungent TRPV1 Agonists, Induce a Mild Hypothermia That Provides Short- and Long-Term Neuroprotection After Ischemic Stroke"]}]}],"canonical_facts":{"dc:contributor":["Sean Marrelli, PhD","Louise D McCullough, MD, PhD","Harry Karmouty-Quintana, PhD"],"dc:creator":["Andersohn, Alexander",""],"dc:date.available":["2025-12-04T08:00:00Z"],"dc:description.abstract":["Therapeutic hypothermia (TH) has demonstrated neuroprotection in instances of cardiac arrest and neonatal hypoxia/ischemia but faces different challenges in application to stroke due to the activation of cold defense mechanisms in conscious patients. This dissertation examines the efficacy and specificity of capsinoids (a purified mixture of capsiate and dihydrocapsiate) to induce a sustained mild hypothermia in conscious mice that is neuroprotective after stroke. Capsinoids function as TRPV1 agonists. However, unlike capsaicin, capsinoids are vulnerable to esterase-mediated breakdown, thus significantly restricting their action to the site of delivery. We showed that capsinoids delivered intraperitoneally (IP) to mice induced a TRPV1-dependent drop in core body temperature into the mild hypothermia range (32-34 °C). Core temperatures dropped without triggering observable cold defense mechanisms (e.g. shivering). The response to capsinoids was dose-dependent and effective in young and aged mice of both sexes. Repeated administration of capsinoids maintained mild hypothermia for up to 6 hours, supporting the potential for applying this cooling procedure for promoting post-stroke TH. Capsinoid-induced hypothermia was linked to an activation of heat defense mechanisms, as evidenced by the rapid induction of cutaneous vasodilation and subsequent drop in core body temperature. We showed that IP capsinoids activate vagal afferents, as demonstrated by an increase in c-Fos positive neurons in the nodose ganglion. Finally, we provide evidence that capsinoid-induced hypothermia is neuroprotective after ischemic stroke and significantly improves short- and long-term outcomes.
"],"dc:identifier":["https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1493"],"dc:subject":["TRPV1","Capsinoid","Capsiate","Ischemic Stroke","Therapeutic Hypothermia","Molecular and Cellular Neuroscience","Neurosciences"],"dc:title":["Capsinoids, Non-Pungent TRPV1 Agonists, Induce a Mild Hypothermia That Provides Short- and Long-Term Neuroprotection After Ischemic Stroke"],"thesis:degree_level":["Dissertation (PhD)"],"thesis:degree_name":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-24T05:50:47Z"}