scholarly journals Novel effect of α-lactalbumin on the yohimbine-induced hot flush increase of the tail skin temperature in ovariectomized rats

2018 ◽  
Vol 82 (5) ◽  
pp. 862-868
Author(s):  
Masayuki Uchida ◽  
Orie Kobayashi
Endocrinology ◽  
2008 ◽  
Vol 149 (10) ◽  
pp. 5219-5226 ◽  
Author(s):  
Peter D. Alfinito ◽  
Xiaohong Chen ◽  
James Atherton ◽  
Scott Cosmi ◽  
Darlene C. Deecher

Previous reports suggest the antiestrogen ICI 182,780 (ICI) does not cross the blood-brain barrier (BBB). However, this hypothesis has never been directly tested. In the present study, we tested whether ICI crosses the BBB, penetrates into brain and hypothalamic tissues, and affects known neuroendocrine functions in ovariectomized rats. Using HPLC with mass spectrometry, ICI (1.0 mg/kg·d, 3 d) was detected in plasma and brain and hypothalamic tissues for up to 24 h with maximum concentrations of 43.1 ng/ml, and 31.6 and 38.8 ng/g, respectively. To evaluate antiestrogenic effects of ICI in the brain after systemic dosing, we tested its ability to block the effect of 17 α-ethinyl estradiol (EE) (0.3 mg/kg, 8 d) on tail-skin temperature abatement in the morphine-dependent model of hot flush and on body weight change. In the morphine-dependent model, EE abated 64% of the naloxone-induced tail-skin temperature increase. ICI pretreatment (1.0, 3.0 mg/kg·d) dose dependently inhibited this effect. ICI (3.0 mg/kg·d) alone showed estrogenic-like actions, abating 30% the naloxone-induced flush. In body weight studies, EE-treated rats weighed 58.5 g less than vehicle-treated rats after 8 d dosing. This effect was partially blocked by ICI (3.0 mg/kg·d) pretreatment. Similar to EE treatment, rats receiving 1.0 or 3.0 mg/kg·d ICI alone showed little weight gain compared with vehicle-treated controls. Thus, ICI crosses the BBB, penetrates into brain and hypothalamic tissues, and has both antiestrogenic and estrogenic-like actions on neuroendocrine-related functions.


Maturitas ◽  
1986 ◽  
Vol 8 (1) ◽  
pp. 67-76 ◽  
Author(s):  
Michael J. Katovich ◽  
James W. Simpkins ◽  
Lee Ann Berglund ◽  
June O'Meara

1992 ◽  
Vol 70 (8) ◽  
pp. 1090-1095 ◽  
Author(s):  
Michael J. Katovich ◽  
David Pitman ◽  
Orit Schechtman

Administration of naloxone to morphine-dependent rats results in an elevation of tail skin temperature and a fall in core temperature. Previous studies have demonstrated a role of the adrenal gland in the thermal responses that accompany morphine withdrawal in the rat. In the present study, experiments were designed to determine if the duration of adrenalectomy significantly influenced the thermal response observed in morphine withdrawal. In addition we evaluated the influence of the adrenal medulla and glucocorticoid replacement in adrenalectomized rats in mediating the thermal responses of the morphine-dependent rat. Ovariectomized rats were addicted to morphine and subsequently withdrawn by administration of naloxone. This treatment results in a significant rise in tail skin temperature and subsequent fall in colonic temperature. These thermal responses were not observed in morphine-naive rats. Adrenalectomy resulted in a significant attenuation of the rise in tail skin temperature associated with withdrawal. This reduced tail skin temperature response was not different among animals adrenalectomized for 1, 7, 14, 21, or 28 days. Likewise, the moderate increase in core temperature associated with morphine treatment was not observed in the adrenalectomized rats. Serum corticosteroid determinations confirmed the loss of the adrenal steroids in the adrenalectomized rats. In a subsequent experiment it was determined that adrenal demedullation did not reduce the tail skin temperature response during morphine withdrawal, and corticosteroids restored the naloxone-induced surge in tail skin temperature in morphine-dependent, adrenalectomized rats. Collectively, these data suggest a role for the adrenal gland, especially the cortical region, in allowing for full expression of the skin temperature changes associated with withdrawal in morphine-dependent animals.Key words: corticosterone, tail skin temperature, morphine withdrawal, adrenal gland, thermal response, naloxone.


2020 ◽  
Vol 20 (6) ◽  
pp. 621-628
Author(s):  
Yanrong Sun ◽  
Qiyue Yang ◽  
Wenpei Bai ◽  
Wenjuan Wang ◽  
Yao Li ◽  
...  

2000 ◽  
Vol 50 (6) ◽  
pp. 651-656
Author(s):  
Tsunefumi Kobayashi ◽  
Mizuho Tamura ◽  
Minoru Hayashi ◽  
Yasuhiro Itano ◽  
Hirofumi Tanabe ◽  
...  

1999 ◽  
Vol 79 ◽  
pp. 281
Author(s):  
Tsunefumi Kobayashi ◽  
Mizuho Tamura ◽  
Minoru Hayashi ◽  
Yasuhiro Katsuura ◽  
Hirofumi Tanabe ◽  
...  

Maturitas ◽  
1991 ◽  
Vol 13 (1) ◽  
pp. 51-63 ◽  
Author(s):  
Mohamad H. Rahimy ◽  
Nicholas Bodorb ◽  
James W. Simpkins

2002 ◽  
Vol 175 (1) ◽  
pp. 177-183 ◽  
Author(s):  
M Noguchi ◽  
Y Ikarashi ◽  
M Yuzurihara ◽  
K Mizoguchi ◽  
K Kurauchi ◽  
...  

We investigated the mechanism for the augmentation of the calcitonin gene-related peptide (CGRP)-induced elevation of skin temperature in ovariectomized (OVX) rats. I.v. injection of alphaCGRP (10 micro g/kg) elevated skin temperature of the hind paws. The elevation was significantly greater in OVX rats than in sham-operated rats and was inhibited by pretreatment with human CGRP(8-37) (100-1000 micro g/kg i.v.), a CGRP receptor antagonist, in a dose-dependent manner. In addition, ovariectomy not only potentiated vasorelaxation due to alphaCGRP but increased the number of CGRP receptors in mesenteric arteries. Further, the plasma concentration of endogenous CGRP was significantly lower in OVX rats. These results suggest that the low concentration of plasma CGRP due to ovarian hormone deficiency may induce the increase in the number of CGRP receptors due to up-regulation. Therefore, the increased number of CGRP receptors may be responsible for potentiation of exogenous alphaCGRP-induced elevation of skin temperature in OVX rats. The mechanism underlying the hot flashes observed in menopausal women may also involve, in part, the up-regulation of CGRP receptors following ovarian hormone deficiency.


2020 ◽  
Vol 70 (1) ◽  
Author(s):  
Shuri Marui ◽  
Yuta Masuda ◽  
Issei Kato ◽  
Kei Nagashima

AbstractThe present study aimed to determine the influence of estradiol (E2) and the interaction with circadian phases on thermoregulatory responses to mild heat in female rats. Heat loss and production during 3-h exposure to the environment at an ambient temperature of 28–34 °C were assessed by measuring abdominal temperature (Tabd), tail skin temperature, and oxygen consumption in ovariectomized rats with and without E2 replacement (OVX + E2 and OVX, respectively) and in control rats in the proestrus (P) and diestrus (D) phases. In the light phase, Tabd remained unchanged in all groups. Tabd increased in the dark phase, but was lower in the OVX + E2 and P groups than in the OVX and D groups. Oxygen consumption decreased at 34 °C, but to a lesser extent in the OVX + E2 group than in the OVX group. These results suggest that E2 activates thermoregulation in mild heat in the dark phase.


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