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1.
Gen Comp Endocrinol ; 252: 36-47, 2017 10 01.
Artigo em Inglês | MEDLINE | ID: mdl-28743556

RESUMO

Thyroid hormones (TH) can increase cellular metabolism. Food deprivation in mammals is typically associated with reduced thyroid gland responsiveness, in an effort to suppress cellular metabolism and abate starvation. However, in prolonged-fasted, elephant seal pups, cellular TH-mediated proteins are up-regulated and TH levels are maintained with fasting duration. The function and contribution of the thyroid gland to this apparent paradox is unknown and physiologically perplexing. Here we show that the thyroid gland remains responsive during prolonged food deprivation, and that its function and production of TH increase with fasting duration in elephant seals. We discovered that our modeled plasma TH data in response to exogenous thyroid stimulating hormone predicted cellular signaling, which was corroborated independently by the enzyme expression data. The data suggest that the regulation and function of the thyroid gland in the northern elephant seal is atypical for a fasted animal, and can be better described as, "adaptive fasting". Furthermore, the modeling data help substantiate the in vivo responses measured, providing unique insight on hormone clearance, production rates, and thyroid gland responsiveness. Because these unique endocrine responses occur simultaneously with a nearly strict reliance on the oxidation of lipid, these findings provide an intriguing model to better understand the TH-mediated reliance on lipid metabolism that is not otherwise present in morbidly obese humans. When coupled with cellular, tissue-specific responses, these data provide a more integrated assessment of thyroidal status that can be extrapolated for many fasting/food deprived mammals.


Assuntos
Jejum/metabolismo , Focas Verdadeiras/metabolismo , Transdução de Sinais , Hormônios Tireóideos/metabolismo , Animais , Jejum/sangue , Iodeto Peroxidase/metabolismo , Modelos Biológicos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Receptores dos Hormônios Tireóideos/metabolismo , Focas Verdadeiras/sangue , Hormônios Tireóideos/sangue , Hormônios Tireóideos/genética
2.
Am J Physiol Regul Integr Comp Physiol ; 310(6): R502-12, 2016 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-26739649

RESUMO

Prolonged food deprivation in mammals typically reduces glucose, insulin, and thyroid hormone (TH) concentrations, as well as tissue deiodinase (DI) content and activity, which, collectively, suppress metabolism. However, in elephant seal pups, prolonged fasting does not suppress TH levels; it is associated with upregulation of adipose TH-mediated cellular mechanisms and adipose-specific insulin resistance. The functional relevance of this apparent paradox and the effects of glucose and insulin on TH-mediated signaling in an insulin-resistant tissue are not well defined. To address our hypothesis that insulin increases adipose TH signaling in pups during extended fasting, we assessed the changes in TH-associated genes in response to an insulin infusion in early- and late-fasted pups. In late fasting, insulin increased DI1, DI2, and THrß-1 mRNA expression by 566%, 44%, and 267% at 60 min postinfusion, respectively, with levels decreasing by 120 min. Additionally, we performed a glucose challenge in late-fasted pups to differentiate between insulin- and glucose-mediated effects on TH signaling. In contrast to the insulin-induced effects, glucose infusion did not increase the expressions of DI1, DI2, and THrß-1 until 120 min, suggesting that glucose delays the onset of the insulin-induced effects. The data also suggest that fasting duration increases the sensitivity of adipose TH-mediated mechanisms to insulin, some of which may be mediated by increased glucose. These responses appear to be unique among mammals and to have evolved in elephant seals to facilitate their adaptation to tolerate an extreme physiological condition.


Assuntos
Tecido Adiposo/efeitos dos fármacos , Tecido Adiposo/metabolismo , Jejum/metabolismo , Glucose/farmacologia , Insulina/farmacologia , Focas Verdadeiras , Transdução de Sinais/efeitos dos fármacos , Hormônios Tireóideos/biossíntese , Animais , Expressão Gênica/efeitos dos fármacos , Sistema Hipotálamo-Hipofisário/efeitos dos fármacos , Infusões Intravenosas , Iodeto Peroxidase/biossíntese , RNA Mensageiro/biossíntese , RNA Mensageiro/genética , Glândula Tireoide/efeitos dos fármacos , Receptores beta dos Hormônios Tireóideos/biossíntese , Hormônios Tireóideos/sangue , Hormônios Tireóideos/genética
3.
J Am Anim Hosp Assoc ; 48(2): 118-24, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22267173

RESUMO

This case describes the presentation and management of an 8 yr old phenotypically female intersex male dog presented for evaluation of a mass in the right inguinal region. The right inguinal space was surgically explored, and a large irregular mass resembling a fully developed testicle was identified in the right vaginal tunic. A second mass resembling an atrophied, but anatomically mature testicle, was identified in the left tunic. The larger mass was identified as a Sertoli cell tumor that had replaced all normal testicular tissue. The smaller mass was identified as a testicle that contained a small intratubular seminoma. The patient was diagnosed as having a phenotypic female sex, chromosomal male sex, and a gonadal male sex. Hormone assays completed before and after the gonadectomy and mass removal document an elevation of circulating progesterone presurgically that returned to baseline by 1 mo postsurgically. The source of the progesterone was identified to be the Leydig cells of the atrophied testicle.


Assuntos
Doenças do Cão/diagnóstico , Doenças do Cão/cirurgia , Neoplasias Testiculares/veterinária , Animais , Doenças do Cão/sangue , Cães , Feminino , Masculino , Fenótipo , Progesterona/sangue , Neoplasias Testiculares/sangue , Neoplasias Testiculares/diagnóstico , Neoplasias Testiculares/cirurgia
4.
Brain Res ; 1148: 205-16, 2007 May 07.
Artigo em Inglês | MEDLINE | ID: mdl-17368429

RESUMO

Thyroid hormones (THs) are important in the development and maturation of the central nervous system (CNS). The significant actions of THs during CNS development occur at the time when TH levels are lower than those in the mother and the hypothalamic-thyroid (HPT) axis is not fully functional. In the developing rat nervous system, primarily the cerebellum, the first three postnatal weeks represent a period of significant sensitivity to thyroid hormones. This study presents a spontaneous, inherited recessive hypothyroidism in Sprague-Dawley rats with devastating functional consequences to the development of the CNS. The clinical signs develop around 14 day's postnatal (dpn) and are characterized by ataxia, spasticity, weight loss and hypercholesterolemia. The afflicted rats died at 30 days due to severe neurological deficits. The deterioration affects the entire CNS and is characterized by progressive neuronal morphological and biochemical changes, demyelination and astrogliosis. The cerebellum, brain stem, neocortex, hippocampus and adrenal gland medulla appear to be most affected. Thyroid Stimulating Hormone (TSH), T3 and T4 levels were significantly lower in hypothyroid rats than control. Immunohistochemistry and RT-PCR demonstrated a reduction of Thyrotropin Releasing Hormone (TRH) in the hypothalamus of hypothyroid rats. The weight of both thyroid and pituitary glands were significantly less in hypothyroid rats than the corresponding normal littermate controls. Transmission electron microscopy demonstrates consistent postsynaptic dendritic, synaptic and spine alterative changes in the brain of hypothyroid rats. These data suggest that we discovered a tertiary form of inherited hypothyroidism involving the hypothalamus.


Assuntos
Encéfalo/anormalidades , Hipotireoidismo Congênito/complicações , Hipotálamo/fisiopatologia , Malformações do Sistema Nervoso/etiologia , Hormônios Tireóideos/metabolismo , Medula Suprarrenal/anormalidades , Medula Suprarrenal/metabolismo , Medula Suprarrenal/fisiopatologia , Animais , Encéfalo/metabolismo , Encéfalo/fisiopatologia , Hipotireoidismo Congênito/metabolismo , Hipotireoidismo Congênito/fisiopatologia , Feminino , Hipotálamo/metabolismo , Masculino , Microscopia Eletrônica de Transmissão , Degeneração Neural/genética , Degeneração Neural/metabolismo , Degeneração Neural/fisiopatologia , Malformações do Sistema Nervoso/metabolismo , Malformações do Sistema Nervoso/fisiopatologia , Neurônios/metabolismo , Neurônios/patologia , Tamanho do Órgão/fisiologia , Hipófise/anormalidades , Hipófise/metabolismo , Hipófise/fisiopatologia , Ratos , Ratos Mutantes , Ratos Sprague-Dawley , Glândula Tireoide/anormalidades , Glândula Tireoide/metabolismo , Glândula Tireoide/fisiopatologia , Tireotropina/metabolismo , Hormônio Liberador de Tireotropina/metabolismo
5.
Contemp Top Lab Anim Sci ; 36(1): 65-68, 1997 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12456188

RESUMO

We evaluated the relationship, in cynomolgus macaques (Mucucufascicularis), between rank for order of blood collection with serum concentrations of 3,5,3 -triiodothyronine (T3), thyroxine (T4), free thyroxine (lT4), and serum cortisol. These relationships were determined for males and females that were housed in two room arrangements. For both room arrangements, males and females were housed separately. For room arrangement 1, macaques were housed on both sides of the animal holding room. The sides of the animal holding room were designated as side A or side B. Blood was initially collected from animals on side A, then from animals on side B. Animals on side B were able to visually observe macaques on side A being physically restrained and sedated for blood collection. In room arrangement 2, the macaques were housed on only one side of the animal holding room and could not directly observe other animals being physically restrained and sedated for blood collection. The relationship for serum lT4 concentration with blood sample collection sequence was different for each room arrangement. For room arrangement 1, we observed an inverse relationship between serum lT4 concentration and the rank for order of blood collection. This finding was observed for males and females and was consistent with the lower serum lT4 value observed for animals housed on room side B. We also observed a trend for higher serum T4 concentration on room side A, but the reverse was true for serum cortisol concentration. In contrast, a macaque s rank for blood collection sequence in room arrangement 2 was not predictive of the rank for serum thyroid hormone (T3, T4, lT4) or serum cortisol concentration. These results suggest that the arrangement of cages in a nonhuman primate holding room contributes to the variability for serum FT4 concentrations.

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