scholarly journals Stomach secretes estrogen in response to blood triglyceride levels in males

2021 ◽  
Author(s):  
Yoshimitsu Kanai ◽  
Takao Ito ◽  
Yuta Yamamoto ◽  
Naoko Yamagishi
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Feeding Behavior ◽  
Fasting Blood Glucose ◽  
Parietal Cells ◽  
Vagal Afferents ◽  
Male Rats ◽  
Glucose Levels ◽  
The Central Nervous System ◽  
Gastric Parietal Cells

Abstract The central nervous system receives body energy information and controls feeding behavior and lipogenesis1. Ghrelin, insulin, leptin and vagal afferents transmit the status of fasting, blood glucose, body fat, and food intake, respectively2-5. Estrogen, which is secreted from adipocytes and gastric parietal cells and from the ovaries in females, also acts upon the central nervous system and liver to inhibit feeding behavior and lipogenesis6-9. How blood triglyceride levels are monitored and how estrogen levels are regulated from the perspective of the lipid homeostasis is not well understood. Using male rats, we show that gastric parietal cells secrete estrogen in response to blood triglyceride levels. Parietal cells predominantly use fatty acid as an energy source. When male rats are administered olive oil or glucose, blood estrogen levels increase as the blood triglyceride, but not glucose, levels rise. Estrogen levels in stomach tissues increase as the blood triglyceride levels rise, and blood triglyceride level-dependent increases of blood estrogen levels are cancelled in gastrectomized rats. We therefore propose that in males, parietal cells in the stomach act as a sensor for the blood triglyceride levels and can secrete estrogen to inhibit the hepatic lipogenesis and feeding behavior when blood triglyceride levels are high.

Apoptosis in rat jejunal mucosa is regulated partly through the central nervous system, which controls feeding behavior

2005 ◽  
Vol 20 (8) ◽  
pp. 1285-1291 ◽  
Author(s):  
TAISAN LIN ◽  
HIROYUKI SAKATA ◽  
AKIFUMI OOTANI ◽  
TAKEHIRO FUJISE ◽  
SEIJI TSUNADA ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Feeding Behavior ◽  
Jejunal Mucosa ◽  
The Central Nervous System

scholarly journals Disrupted Leptin Signaling in the Lateral Hypothalamus and Ventral Premammillary Nucleus Alters Insulin and Glucagon Secretion and Protects Against Diet-Induced Obesity

Endocrinology ◽  
2016 ◽  
Vol 157 (7) ◽  
pp. 2671-2685 ◽  
Author(s):  
Heather C. Denroche ◽  
Maria M. Glavas ◽  
Eva Tudurí ◽  
Subashini Karunakaran ◽  
Whitney L. Quong ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Weight Gain ◽  
Blood Glucose ◽  
Glucagon Secretion ◽  
Hypothalamic Nucleus ◽  
Leptin Signaling ◽  
Glucose Levels ◽  
The Central Nervous System

Leptin signaling in the central nervous system, and particularly the arcuate hypothalamic nucleus, is important for regulating energy and glucose homeostasis. However, the roles of extra-arcuate leptin responsive neurons are less defined. In the current study, we generated mice with widespread inactivation of the long leptin receptor isoform in the central nervous system via Synapsin promoter-driven Cre (Leprflox/flox Syn-cre mice). Within the hypothalamus, leptin signaling was disrupted in the lateral hypothalamic area (LHA) and ventral premammillary nucleus (PMV) but remained intact in the arcuate hypothalamic nucleus and ventromedial hypothalamic nucleus, dorsomedial hypothalamic nucleus, and nucleus of the tractus solitarius. To investigate the role of LHA/PMV neuronal leptin signaling, we examined glucose and energy homeostasis in Leprflox/flox Syn-cre mice and Leprflox/flox littermates under basal and diet-induced obese conditions and tested the role of LHA/PMV neurons in leptin-mediated glucose lowering in streptozotocin-induced diabetes. Leprflox/flox Syn-cre mice did not have altered body weight or blood glucose levels but were hyperinsulinemic and had enhanced glucagon secretion in response to experimental hypoglycemia. Surprisingly, when placed on a high-fat diet, Leprflox/flox Syn-cre mice were protected from weight gain, glucose intolerance, and diet-induced hyperinsulinemia. Peripheral leptin administration lowered blood glucose in streptozotocin-induced diabetic Leprflox/flox Syn-cre mice as effectively as in Leprflox/flox littermate controls. Collectively these findings suggest that leptin signaling in LHA/PMV neurons is not critical for regulating glucose levels but has an indispensable role in the regulation of insulin and glucagon levels and, may promote the development of diet-induced hyperinsulinemia and weight gain.

Oxytocin in the central nervous system and sexual behaviour in male rats

1987 ◽  
Vol 414 (1) ◽  
pp. 133-137 ◽  
Author(s):  
Andy M. Hughes ◽  
Barry J. Everitt ◽  
Stafford L. Lightman ◽  
Kathryn Todd
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Sexual Behaviour ◽  
Male Rats ◽  
The Central Nervous System

scholarly journals Oestrogenic effects of neonatal administration of raloxifene on hypothalamic-pituitary-gonadal axis in male and female rats

Reproduction ◽  
2001 ◽  
pp. 915-924 ◽  
Author(s):  
L Pinilla ◽  
LC Gonzalez ◽  
F Gaytan ◽  
M Tena-Sempere ◽  
E Aguilar
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Body Weight ◽  
Oestrogen Receptor ◽  
Female Rats ◽  
Male Rats ◽  
Selective Oestrogen Receptor Modulators ◽  
Male And Female Rats ◽  
The Central Nervous System ◽  
Neonatal Administration

Selective oestrogen receptor modulators constitute a family of drugs that are used increasingly in the management of oestrogen-associated pathology. Raloxifene is a selective oestrogen receptor modulator that is used to treat and prevent osteoporosis in post-menopausal women. The actions of raloxifene on bone, breast, uterus and serum cholesterol concentrations have been widely analysed, but very few studies have investigated the possible actions of this drug on the central nervous system. The central nervous system of the newborn rat is very sensitive to oestrogen action. In this study a series of experiments was conducted to analyse the effects of different doses of raloxifene (50, 100, 250 or 500 microg per rat per day) administered to neonatal rats on days 1-5 of age. Female rats treated with raloxifene showed decreased gonadotrophin secretion, hyperprolactinaemia, advanced vaginal opening, decreased body weight, persistent presence of cornified epithelial cells in vaginal smears, anovulation, inhibition of positive feedback between oestradiol and LH, and infertility. Male rats showed delayed balanopreputial separation, reduced body weight and hyperprolactinaemia. All these changes resemble those obtained after neonatal administration of oestradiol benzoate, thus indicating, for the first time, that raloxifene exerts an oestrogenic action on the hypothalamic-pituitary structures controlling reproductive function in rats.

scholarly journals Stomach secretes estrogen in response to the blood triglyceride levels

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Takao Ito ◽  
Yuta Yamamoto ◽  
Naoko Yamagishi ◽  
Yoshimitsu Kanai
Keyword(s):  
Feeding Behavior ◽  
Body Fat ◽  
Energy Homeostasis ◽  
Fasting Blood Glucose ◽  
Gastric Gland ◽  
Vagal Afferents ◽  
Dependent Manner ◽  
The Status ◽  
Gastric Parietal Cells ◽  
Body Energy

AbstractMammals receive body energy information to maintain energy homeostasis. Ghrelin, insulin, leptin and vagal afferents transmit the status of fasting, blood glucose, body fat, and food intake, respectively. Estrogen also inhibits feeding behavior and lipogenesis, but increases body fat mass. However, how blood triglyceride levels are monitored and the physiological roles of estrogen from the perspective of lipid homeostasis remain unsettled. Here, we show that stomach secretes estrogen in response to the blood triglyceride levels. Estrogen-secreting gastric parietal cells predominantly use fatty acids as an energy source. Blood estrogen levels increase as blood triglyceride levels rise in a stomach-dependent manner. Estrogen levels in stomach tissues increase as blood triglyceride levels rise, and isolated gastric gland epithelium produces estrogen in a fatty acid-dependent manner. We therefore propose that stomach monitors and controls blood triglyceride levels using estrogen, which inhibits feeding behavior and lipogenesis, and promotes triglyceride uptake by adipocytes.

EFFECTS OF ADRENAL ANDROGEN IN THE CENTRAL NERVOUS SYSTEM ON BLADDER FUNCTION IN MALE RATS

2009 ◽  
Vol 181 (4S) ◽  
pp. 81-82
Author(s):  
Yoshiji Miwa ◽  
Keiko Nagase ◽  
Taisei Kaneda ◽  
Nobuyuki Oyama ◽  
Hironobu Akino ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Male Rats ◽  
Bladder Function ◽  
Adrenal Androgen ◽  
The Central Nervous System

THE INFLUENCE OF SEX ON THE MATURATION OF THE CENTRAL NERVOUS SYSTEM IN THE ALBINO RAT

1951 ◽  
Vol 7 (3) ◽  
pp. 271-279 ◽  
Author(s):  
J. T. EAYRS
Keyword(s):  
Spinal Cord ◽  
Central Nervous System ◽  
Nervous System ◽  
The Body ◽  
Female Rats ◽  
Male Rats ◽  
Albino Rat ◽  
Litter Mate ◽  
Male And Female Rats ◽  
The Central Nervous System

The growth of the body and central nervous system and the emergence of stereotyped behaviour have been studied in male and female rats during the first 24 days of life. The effects of daily injections of equine gonadotrophin on these measures have also been investigated. The weight of the body and of the central nervous system was significantly less in the female than in the male. The daily administration of 10 i.u. of equine gonadotrophin was without effect on either. The movements of the trunk and limbs concerned in the body-righting reflex became coordinated more slowly in the gonadotrophin-injected animals than in their litter-mate controls. At 15 days old, male rats were able to right in mid-air more successfully than litter-mate females. The placing reflex appeared earlier in the male than in the female. Its appearance was accelerated in the females given gonadotrophin, but not in the males. In the ventral funiculus of the spinal cord of 24-day-old experimental animals, the axis cylinders occupied more space relative to that occupied by myelin than did those of the controls. The total amount of myelin present was unchanged. There was no sex difference in the progress of myelination in the spinal cord. The significance of these findings in relation to the secretion of sex hormones is discussed. It is suggested that the secretion of androgen may be responsible for an acceleration of nervous maturation.

scholarly journals Proposal of open field test as a model of varenicline pharmacokinetic study in rats

2018 ◽  
Vol 11 (3) ◽  
Author(s):  
Julia Zaccarelli-Magalhães ◽  
Thaisa Meira Sandini ◽  
André Rinaldi Fukushima ◽  
Helenice De Souza Spinosa
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Single Dose ◽  
Open Field ◽  
Field Test ◽  
Open Field Test ◽  
Male Rats ◽  
Control Group ◽  
Immobility Time ◽  
The Central Nervous System

Varenicline is a medication used for smoking treatment that acts as a partial agonist for nicotinic cholinergic receptors α4β2 and α3β4 and as a total agonist of receptor α7 in the central nervous system. Pharmacokinetic is important information for medications that acts in the central nervous system. This kind of assay is commonly done by expensive and complex analytical techniques. Therefore, the aim of this study was to evaluate the possibility of using the open field test as a pharmacokinetic model for varenicline in male rats exposed to a single dose of varenicline. Male rats received a single dose orally (gavage) of three different concentrations of varenicline: 0.03 (therapeutic dose for humans), 0.1 and 0.3 mg/kg or water (control group). The open field observations were recorded 30 min, 1, 2, 4, 6, 24, 48, 72 h and 7 days after the administration of varenicline or water. The results showed alterations in locomotion and rearing frequencies, as well as in immobility time observed in open field, which is consistent with this drug’s plasma peak. Consequently, this behavioral test apparently can be considerate as a model for pharmacokinetic evaluation of varenicline.

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