TY - JOUR
T1 - Fasting or systemic des-acyl ghrelin administration to rats facilitates thermoregulatory behavior in a cold environment
AU - Uchida, Yuki
AU - Nagashima, Kei
AU - Yuri, Kazunari
N1 - Funding Information:
We are grateful to Mrs. Miwa Kono, Mr. Masayuki Sakano, Dr. Yoji Osako (Kochi University), and Dr. Keiko Morimoto (Nara Women’s University) for their support of this research. The present research was partly supported by the Japan Society for the Promotion of Science; Grant-in-Aid for Young Scientists (Start-up), No. 24800047; Grant-in-Aid for Young Scientists (B), No. 26870417; Kochi University; Grant for Young Scientists (Start-up).
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Fasted rats place their tails underneath their body trunks in the cold (tail-hiding behavior), which is a thermoregulatory behavior. The aim of the present study was to investigate the effect of fasting and des-acyl ghrelin, a hormone related to fasting, on tail-hiding behavior and neural activity in the cold. Wistar rats were divided into ‘fed’ ‘42-h fasting’ and des-acyl ghrelin groups. The rats received an intraperitoneal saline or 30-μg des-acyl ghrelin injection, and were then exposed to 27 °C or 15 °C for 2-h with continuous body temperature (T b ), tail skin temperature (T tail ), and tail-hiding behavior measurements. cFos immunoreactive (cFos-IR) cells in the insula, secondary somatosensory cortex, medial preoptic nucleus, parastrial nucleus, amygdala, and lateral parabrachial nucleus were counted in four segments: seg1, 2, 3, and 4 (bregma −0.36, −1.44, −2.64, and −9.00 mm), respectively. At 15 °C, T b and T tail were lower in the 42-h fasting group than in the fed and des-acyl ghrelin groups, and the duration of tail-hiding behavior was longer in the 42-h fasting and des-acyl ghrelin groups than in the fed group. The onset of tail-hiding behavior more advanced in the des-acyl ghrelin group than in the fed group at 15 °C. Only at the insula in seg3 at 15 °C, the number of cFos-IR cells was greater in the 42-h fasting group than in the fed group. Both the 42-h fasting and des-acyl ghrelin groups might modulate the tail-hiding behavior of rats in a cold, and a part of the insula might be involved this response during fasting.
AB - Fasted rats place their tails underneath their body trunks in the cold (tail-hiding behavior), which is a thermoregulatory behavior. The aim of the present study was to investigate the effect of fasting and des-acyl ghrelin, a hormone related to fasting, on tail-hiding behavior and neural activity in the cold. Wistar rats were divided into ‘fed’ ‘42-h fasting’ and des-acyl ghrelin groups. The rats received an intraperitoneal saline or 30-μg des-acyl ghrelin injection, and were then exposed to 27 °C or 15 °C for 2-h with continuous body temperature (T b ), tail skin temperature (T tail ), and tail-hiding behavior measurements. cFos immunoreactive (cFos-IR) cells in the insula, secondary somatosensory cortex, medial preoptic nucleus, parastrial nucleus, amygdala, and lateral parabrachial nucleus were counted in four segments: seg1, 2, 3, and 4 (bregma −0.36, −1.44, −2.64, and −9.00 mm), respectively. At 15 °C, T b and T tail were lower in the 42-h fasting group than in the fed and des-acyl ghrelin groups, and the duration of tail-hiding behavior was longer in the 42-h fasting and des-acyl ghrelin groups than in the fed group. The onset of tail-hiding behavior more advanced in the des-acyl ghrelin group than in the fed group at 15 °C. Only at the insula in seg3 at 15 °C, the number of cFos-IR cells was greater in the 42-h fasting group than in the fed group. Both the 42-h fasting and des-acyl ghrelin groups might modulate the tail-hiding behavior of rats in a cold, and a part of the insula might be involved this response during fasting.
KW - Des-acyl ghrelin
KW - Fasting
KW - Tail skin temperature
KW - Tail-hiding behavior
KW - cFos
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U2 - 10.1016/j.brainres.2018.05.038
DO - 10.1016/j.brainres.2018.05.038
M3 - Article
C2 - 29859973
AN - SCOPUS:85047897326
SN - 0006-8993
VL - 1696
SP - 10
EP - 21
JO - Brain Research
JF - Brain Research
ER -