Evaluation of Thyroid Function in North Indians with Alopecia Areata: Response to Intravenous Injection of 100 μg Thyrotropin Releasing Hormone (TRH)

1999 ◽  
Vol 26 (6) ◽  
pp. 339-342 ◽  
Author(s):  
Vinod K Sharma ◽  
Ravinder Sialy ◽  
Bhushan Kumar ◽  
Somesh Gupta
2021 ◽  
pp. 1-30
Author(s):  
Ying Sun ◽  
Xin Du ◽  
Zhongyan Shan ◽  
Weiping Teng ◽  
Yaqiu Jiang

Abstract Iodine is an important element in thyroid hormone biosynthesis. Thyroid function is regulated by the hypothalamic-pituitary-thyroid axis (HPT). Excessive iodine leads to elevated thyroid stimulating hormone (TSH) levels, but the mechanism is not yet clear. Type 2 deiodinase (Dio2) is a selenium-containing protease that plays a vital role in thyroid function. The purpose of this study was to explore the role of hypothalamus Dio2 in regulating TSH increase caused by excessive iodine and to determine the effects of iodine excess on thyrotropin-releasing hormone (TRH) levels. Male Wistar rats were randomized into five groups and administered different iodine dosages (folds of physiological dose): normal iodine (NI), 3-fold iodine (3HI), 6-fold iodine (6HI), 10-fold iodine (10HI), and 50-fold iodine (50HI). Rats were euthanized at 4, 8, 12, or 24 weeks after iodine administration. Serum TRH, TSH, total thyroxine (TT4), and total triiodothyronine (TT3) were determined. Hypothalamus tissues were frozen and sectioned to evaluate expression of Dio2, Dio2 activity, and monocarboxylate transporter 8 (MCT8). Prolonged high iodine intake significantly increased TSH expression (p < 0.05), but did not affect TT3 and TT4 levels. Prolonged high iodine intake decreased serum TRH levels in the hypothalamus (p < 0.05). Dio2 expression and activity in the hypothalamus exhibited an increasing trend compared at each time point with increasing iodine intake (p < 0.05). Hypothalamic MCT8 expression was increased in rats with prolonged high iodine intake(p < 0.05). These results indicate that iodine excess affects the levels of Dio2, TRH, and MCT8 in the hypothalamus.


1974 ◽  
Vol 52 (5) ◽  
pp. 1012-1019 ◽  
Author(s):  
A. Dupont ◽  
F. Labrie ◽  
L. Levasseur ◽  
A. V. Schally

Thirty seconds after an intravenous injection of 0.5 ml of 2.5 × 10−6 M [3H]thyrotropin-releasing hormone (TRH) to male rats, the radioactivity was distributed in an apparent volume of 134 ml, thus reflecting its rapid disappearance from the blood. The pattern of plasma radioactivity after intravenous injection of [3H]TRH could be represented by the sum of three exponentials, suggesting a three-compartment model of plasma disappearance of radioactivity. The half-life of TRH and of its metabolites calculated from the first exponential curve was 2.2 min. Thin-layer electrophoresis of methanol extracts of plasma collected 1, 7, 20, and 30 min after injection of [3H]TRH showed that the neurohormone was transformed into TRH-free acid in proportions of 58, 58, 52, and 47%, respectively. The first 60 min seemed to be the most important period for elimination of the hormone and its metabolites by the kidney. In fact, 60 min after injection, 38% of the total radioactivity was found in the bladder. At 2, 15, and 30 min after injection of [3H]TRH, high accumulation of radioactivity occurred in kidneys, pineal gland, and anterior and posterior (including intermediate) lobes of the pituitary. High levels of radioactivity were seen in kidneys and anterior pituitary gland at all time intervals studied.


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