4.5 Article

Transplantation of Human Dental Pulp-Derived Stem Cells Protects Against Heatstroke in Mice

期刊

CELL TRANSPLANTATION
卷 24, 期 5, 页码 921-937

出版社

COGNIZANT COMMUNICATION CORP
DOI: 10.3727/096368914X678580

关键词

Heatstroke; Human exfoliated deciduous teeth pulp stem cells; Brain; Thermoregulation; Neurologic severity scores; Multiple organs

资金

  1. National Science Council of the Republic of China [NSC100-2314-B-218-001, NSC102-2628-B-384-001-MY3]
  2. Department of Health of the Republic of China (Center of Excellence for Clinical Trial and Research in Neuroscience) [DOH99-TD-B-111-003]

向作者/读者索取更多资源

Stem cells from human exfoliated deciduous tooth pulp (SHED) is a promising approach for the treatment of stroke and spinal cord injury. In this study, we investigated the therapeutic effects of SHED for the treatment of multiple organ (including brain, particularly hypothalamus) injury in heatstroke mice. ICR male mice were exposed to whole body heating (WBH; 41.2 degrees C, relative humidity 50-55%, for 1 h) and then returned to normal room temperature (26 degrees C). We observed that intravenous administration of SHED immediately post-WBH exhibited the following therapeutic benefits for recovery after heatstroke: (a) inhibition of WBH-induced neurologic and thermoregulatory deficits; (b) reduction of WBH-induced ischemia, hypoxia, and oxidative damage to the brain (particularly the hypothalamus); (c) attenuation of WBH-induced increased plasma levels of systemic inflammatory response molecules, such as tumor necrosis factor-alpha and intercellular adhesion molecule-1; (d) improvement of WBH-induced hypothalamo pituitary adrenocortical (HPA) axis activity (as reflected by enhanced plasma levels of both adrenocorticotrophic hormone and corticosterone); and (e) attenuation of WBH-induced multiple organ apoptosis as well as lethality. In conclusion, post-WBH treatment with SHED reduced induction of proinflammatory cytokines and oxidative radicals, enhanced plasma induction of both adrenocorticotrophic hormone and corticosterone, and improved lethality in mouse heatstroke. The protective effect of SHED may be related to a decreased inflammatory response, decreased oxidative stress, and an increased HPA axis activity following the WBH injury.

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