TY - JOUR
T1 - Browning and beiging of adipose tissue, its role in the regulation of energy homeostasis and as a potential target for alleviating metabolic diseases
T2 - Brown adipose tissue activation in a rat model of parkinson’s disease
AU - Wang, Wenjuan
AU - Meng, Xiangzhi
AU - Yang, Chun
AU - Fang, Dongliang
AU - Wang, Xuemeng
AU - An, Jiaqiang
AU - Zhang, Jingyi
AU - Wang, Lulu
AU - Lu, Tao
AU - Ruan, Hai Bin
AU - Gao, Yan
N1 - Publisher Copyright:
© 2017 the American Physiological Society.
PY - 2017/12/6
Y1 - 2017/12/6
N2 - Loss of body weight and fat mass is one of the nonmotor symptoms of Parkinson’s disease (PD). Weight loss is due primarily to reduced energy intake and increased energy expenditure. Whereas inadequate energy intake in PD patients is caused mainly by appetite loss and impaired gastrointestinal absorption, the underlying mechanisms for increased energy expenditure remain largely unknown. Brown adipose tissue (BAT), a key thermogenic tissue in humans and other mammals, plays an important role in thermoregulation and energy metabolism; however, it has not been tested whether BAT is involved in the negative energy balance in PD. Here, using the 6-hydroxydopamine (6-OHDA) rat model of PD, we found that the activity of sympathetic nerve (SN), the expression of Ucp1 in BAT, and thermogenesis were increased in PD rats. BAT sympathetic denervation blocked sympathetic activity and decreased UCP1 expression in BAT and attenuated the loss of body weight in PD rats. Interestingly, sympathetic denervation of BAT was associated with decreased sympathetic tone and lipolysis in retroperitoneal and epididymal white adipose tissue. Our data suggeste that BAT-mediated thermogenesis may contribute to weight loss in PD.
AB - Loss of body weight and fat mass is one of the nonmotor symptoms of Parkinson’s disease (PD). Weight loss is due primarily to reduced energy intake and increased energy expenditure. Whereas inadequate energy intake in PD patients is caused mainly by appetite loss and impaired gastrointestinal absorption, the underlying mechanisms for increased energy expenditure remain largely unknown. Brown adipose tissue (BAT), a key thermogenic tissue in humans and other mammals, plays an important role in thermoregulation and energy metabolism; however, it has not been tested whether BAT is involved in the negative energy balance in PD. Here, using the 6-hydroxydopamine (6-OHDA) rat model of PD, we found that the activity of sympathetic nerve (SN), the expression of Ucp1 in BAT, and thermogenesis were increased in PD rats. BAT sympathetic denervation blocked sympathetic activity and decreased UCP1 expression in BAT and attenuated the loss of body weight in PD rats. Interestingly, sympathetic denervation of BAT was associated with decreased sympathetic tone and lipolysis in retroperitoneal and epididymal white adipose tissue. Our data suggeste that BAT-mediated thermogenesis may contribute to weight loss in PD.
UR - http://www.scopus.com/inward/record.url?scp=85037660940&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85037660940&partnerID=8YFLogxK
U2 - 10.1152/ajpendo.00049.2017
DO - 10.1152/ajpendo.00049.2017
M3 - Article
C2 - 28851733
AN - SCOPUS:85037660940
SN - 0193-1849
VL - 313
SP - E731-E736
JO - American Journal of Physiology - Endocrinology and Metabolism
JF - American Journal of Physiology - Endocrinology and Metabolism
IS - 6
ER -