Effect of neonatal hypothyroidism on maturation of nuclear triiodothyronine (T3) receptors in developing rat brain

1980 ◽  
Vol 95 (4) ◽  
pp. 495-499 ◽  
Author(s):  
Kazumasa Ishiguro ◽  
Yukichi Suzuki ◽  
Tamotu Sato
Keyword(s):  
Rat Brain ◽  
Binding Capacity ◽  
Physiological Role ◽  
Brain Maturation ◽  
Control Group ◽  
High Concentration ◽  
Neonatal Hypothyroidism ◽  
Developing Rat ◽  
T3 Receptors

Abstract. Changes of nuclear T3 receptors during brain maturation were studied in normal and hypothyroid rats. In normal rats, the higher receptor concentration present in the neonatal period (0.35 ± 0.04 ng T3/mg DNA) decreased at the age of 14 days (0.25 ± 0.02 ng T3/mg DNA), and remained at this level thereafter to 35 days of age (0.25 ± 0.03 T3/mg DNA). In contrast, hypothyroid rats showed a significantly higher concentration than that found in an age-matched control group at the age of 14 days (0.38 ± 0.07 ng T3/mg DNA), and maintained this level up to 35 days of age (0.37 ± 0.03 T3/mg DNA). The binding affinity was similar in both groups and throughout maturation (mean ± sd in normal groups: 1.9 ± 0.3 × 1010m−1, in hypothyroid groups: 1.7 ± 0.2 × 1010m−1). Plasma T3 concentrations showed changes reciprocal to those in the binding capacity of T3 receptors. These results indicate that nuclear T3 receptors in rat brain mature by the age of 14 days, in association with a decrease in binding capacity, and this process seems to be T3-dependent. The physiological role of the high concentration of T3 receptors observed in neonatal and hypothyroid rat brain during development is at present not clear.

Regulation of tubulin by triiodothyronine in hypothyroid rat brain

1985 ◽  
Vol 5 (8) ◽  
pp. 643-648 ◽  
Author(s):  
Anjana Mazumder ◽  
Kamal Das ◽  
Pranab K. Sarkar
Keyword(s):  
Protein Synthesis ◽  
Rat Brain ◽  
Brain Maturation ◽  
Normal Brain ◽  
Neonatal Brain ◽  
Organ Cultures ◽  
Postnatal Brain ◽  
Enhanced Sensitivity ◽  
Brain Exposure ◽  
Developing Rat

The effect of T3 (triiodothyronine) on the induction of tubulin in hypothyroid developing rat brain has been examined using organ cultures of brains from late fetal, neonatal and postnatalrats. The neonatal brain displayed maximum sensitivity to T3. Hypothyroidism resulted in a 26% decline in the level of tubulin in the neonatal brain as opposed to a 5–15% decline in the fetal or postnatal brain. Exposure of the hypothyroi d neonatal brain to T3 for 2 h in culture led to a 61% rise in the level of tubulin in contrast to a 41% increase seen in the case of normal brain. Total protein synthesis was not significantly affected. The preferential decline of tubulin in the neonatal hypothyroid brain, its enhanced sensitivity to T3 compared to normal brain, and the coincidence of the period of sensitivity to that of brain maturation indicate that the regulation of the level of tubulin by T3 in the developing brain is a natural ontogenic phenomenon.

scholarly journals Activation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase in homogenates of developing rat brain

1979 ◽  
Vol 182 (2) ◽  
pp. 367-370 ◽  
Author(s):  
W A Maltese ◽  
J J Volpe
Keyword(s):  
Rat Brain ◽  
Cholesterol Synthesis ◽  
Specific Activity ◽  
Postnatal Period ◽  
Developing Brain ◽  
Brain Maturation ◽  
Assay Mixture ◽  
Coa Reductase ◽  
Developing Rat ◽  
Homogenization Medium

The specific activity of 3-hydroxy-3-methylglutaryl-CoA reductase increases when homogenates of developing rat brain are incubated at 37 degrees C or kept on ice. This increase is completely blocked by the addition of F- to the homogenization medium and the assay mixture. The capacity for activation of the reductase is greatest during the early postnatal period and declines as brain maturation proceeds. The data suggest that catalytic modification of the reductase may play a role in the regulation of cholesterol synthesis in the developing brain.

scholarly journals Role of acute phase proteins in diagnosis of uremic pancreatitis and destructive pancreatitis in patients receiving renal replacement therapy (programmed hemodialysis)

2021 ◽  
Vol 38 (5) ◽  
pp. 115-122
Author(s):  
Kazim G. Gasanov ◽  
Viktor A. Zurnadzhyants ◽  
Eldar A. Kchibekov ◽  
M. I. Shikhragimov
Keyword(s):  
Renal Replacement Therapy ◽  
Serum Concentration ◽  
Blood Serum ◽  
Replacement Therapy ◽  
Acute Phase Proteins ◽  
Control Group ◽  
Serum Concentrations ◽  
High Concentration ◽  
Surgical Unit

Objective. To determine the blood serum 2-microglobulin and 2-macroglobulin concentration in patients undergoing renal replacement therapy (programmed hemodialysis) for the diagnosis of uremic pancreatitis and / or destructive pancreatitis. Materials and methods. The study involved 52 patients admitted to the Surgical Unit of Astrakhan "RZhD-Medicine" Hospital and City Clinical Hospital № 3. The blood serum 2-microglobulin and 2-macroglobulin concentration was analyzed in patients admitted on an emergency basis with suspicion of uremic pancreatitis and destructive pancreatitis, who receive renal replacement therapy (programmed hemodialysis). The control group included 50 outpatients undergoing renal replacement therapy (programmed hemodialysis). The study did not include patients with suspected pancreatitis who were not receiving renal replacement therapy. The period of the study is 20192021. Results. The concentration of blood serum 2-microglobulin is statistically higher than normal in all patients, who had received renal replacement therapy (programmed hemodialysis) in anamnesis. The most statistically high concentration of 2-microglobulin was revealed while studying patients with uremic pancreatitis (n = 34), and was (30.0 2.75 mg/l) compared with the blood serum concentration in patients with destructive pancreatitis (8 0.51 mg / l). The concentration of 2-macroglobulin was statistically lower in destructive pancreatitis (n = 18) and was 615 161 mg/l compared with uremic pancreatitis (980 216 mg/l). In the control group of outpatients (n = 50) receiving renal replacement therapy (programmed hemodialysis), no statistically significant blood serum concentrations of 2-microglobulin and 2-macroglobulin were found. Conclusions. A clear dependence of the concentration of 2-microglobulin and 2-macroglobulin on the severity of uremic pancreatitis and destructive pancreatitis was established. Statistically high values of 2-microglobulin concentrations were obtained in patients with uremic pancreatitis, and the 2-macroglobulin level was statistically low in destructive pancreatitis.

scholarly journals Leptin down-regulates KCC2 activity and controls chloride homeostasis in the neonatal rat hippocampus

2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Camille Dumon ◽  
Yasmine Belaidouni ◽  
Diabe Diabira ◽  
Suzanne M. Appleyard ◽  
Gary A. Wayman ◽  
...  
Keyword(s):  
Neurological Disorders ◽  
Physiological Role ◽  
Rat Hippocampus ◽  
Neonatal Rat ◽  
Chloride Homeostasis ◽  
Hypothalamic Nuclei ◽  
Hippocampal Networks ◽  
Developing Rat

Abstract The canonical physiological role of leptin is to regulate hunger and satiety acting on specific hypothalamic nuclei. Beyond this key metabolic function; leptin also regulates many aspects of development and functioning of neuronal hippocampal networks throughout life. Here we show that leptin controls chloride homeostasis in the developing rat hippocampus in vitro. The effect of leptin relies on the down-regulation of the potassium/chloride extruder KCC2 activity and is present during a restricted period of postnatal development. This study confirms and extends the role of leptin in the ontogenesis of functional GABAergic inhibition and helps understanding how abnormal levels of leptin may contribute to neurological disorders.

INFLUENCE OF NEONATAL HYPOTHYROIDISM ON AMINO ACIDS IN DEVELOPING RAT BRAIN

1966 ◽  
Vol 13 (10) ◽  
pp. 1017-1025 ◽  
Author(s):  
Alicia E. Ramírez De Guglielmone ◽  
Carlos J. Gómez
Keyword(s):  
Amino Acids ◽  
Rat Brain ◽  
Neonatal Hypothyroidism ◽  
Developing Rat

scholarly journals Leptin down-regulates KCC2 activity and controls chloride homeostasis in the neonatal rat hippocampus.

2020 ◽  
Author(s):  
Camille Dumon ◽  
Yasmine Belaidouni ◽  
Diabe Diabira ◽  
Suzanne Appleyard ◽  
Gary Wayman ◽  
...  
Keyword(s):  
Neurological Disorders ◽  
Physiological Role ◽  
Rat Hippocampus ◽  
Neonatal Rat ◽  
Chloride Homeostasis ◽  
Hypothalamic Nuclei ◽  
Hippocampal Networks ◽  
Developing Rat

Abstract The canonical physiological role of leptin is to regulate hunger and satiety acting on specific hypothalamic nuclei. Beyond this key metabolic function; leptin also regulates many aspects of development and functioning of neuronal hippocampal networks throughout life. Here we show that leptin controls chloride homeostasis in the developing rat hippocampus in vitro. The effect of leptin relies on the down-regulation of the potassium/chloride extruder KCC2 activity and is present during a restricted period of postnatal development. This study confirms and extends the role of leptin in the ontogenesis of functional GABAergic inhibition and helps understanding how abnormal levels of leptin may contribute to neurological disorders.

Aluminium-Induced Behavioral Changes and Oxidative Stress in Developing Rat Brain and the Possible Ameliorating Role of Omega-6/Omega-3 Ratio

2017 ◽  
Vol 17 (3) ◽  
pp. 106-117 ◽  
Author(s):  
Imene Benyettou ◽  
Omar Kharoubi ◽  
Nouria Hallal ◽  
Hadj Ali Benyettou ◽  
Kaddour Tair ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Rat Brain ◽  
Behavioral Changes ◽  
Omega 3 ◽  
Omega 6 ◽  
Developing Rat ◽  
And Oxidative Stress

scholarly journals Physiological role of a novel neuropeptide, apelin, and its receptor in the rat brain

2001 ◽  
Vol 77 (4) ◽  
pp. 1085-1096 ◽  
Author(s):  
Annabelle Reaux ◽  
Nadia De Mota ◽  
Ivana Skultetyova ◽  
Zsolt Lenkei ◽  
Said El Messari ◽  
...  
Keyword(s):  
Rat Brain ◽  
Physiological Role

Selective alterations in hepatic nuclear T3-receptors and enzyme responses by glucocorticoid deficit or excess

1983 ◽  
Vol 104 (4) ◽  
pp. 485-489 ◽  
Author(s):  
Alfredo R. Recúpero ◽  
Aldo H. Coleoni ◽  
Olga Cherubini ◽  
Adriana Oviedo
Keyword(s):  
Binding Capacity ◽  
Receptor Site ◽  
In Vitro Assays ◽  
Control Group ◽  
Basal Activity ◽  
Glycerophosphate Dehydrogenase ◽  
Vitro Effect ◽  
T3 Receptors ◽  
Apparent Association

Abstract. Glucocorticoid deficit in rats induced by adrenalectomy for a 10-day period resulted in an increase in the apparent association constant (Ka) of the liver nuclear T3-receptor while maximal binding capacity (MBC) remained unaltered compared to the intact (sham-operated) animals and to adrenalectomy plus dexamethasone (Sx + D) animals. In addition, a significant increase in the basal activity of liver mitochondrial α-glycerophosphate dehydrogenase (α-GPD) was observed, while cytosolic malic enzyme (ME) activity was not modified in this situation. Dexamethasone injection (5 mg/kg/day for 4–5 days) to previously adrenalectomized animals (Sx + D) induced a significant increase in MBC of nuclear T3-receptors. On the other hand, Ka value and α-GPD activity were restored to the values found in the control group. However, basal activity of ME as well as the response of this enzyme to a saturating dose of T3 was substantially increased by dexamethasone treatment. A non-specific in vitro effect of dexamethasone on MBC and ME was excluded as these parameters were not modified when dexamethasone was added immediately before the in vitro assays. The present study indicates that glucocorticoid deficit or excess is able to induce changes at the level of the nuclear T3-receptor site. The increase in the activity of cytolic ME induced by dexamethasone injection was associated with a simultaneous

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