Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
SUMMARYFood deprivation in mammals is typically associated with reduced thyroid hormone (TH) concentrations and deiodinase content and activity to suppress metabolism. However, in prolonged-fasted, metabolically active elephant seal pups, TH levels are maintained, if not elevated. The functional relevance of this apparent paradox is unknown and demonstrates variability in the regulation of TH levels, metabolism and function in food-deprived mammals. To address our hypothesis that cellular TH-mediated activity is upregulated with fasting duration, we quantified the mRNA expression and protein content of adipose and muscle deiodinase type I (DI1) and type II (DI2), and TH receptor beta-1 (THrβ-1) after 1, 3 and 7 weeks of fasting in northern elephant seal pups (N=5-7 per week). Fasting did not decrease the concentrations of plasma thyroid stimulating hormone, total triiodothyronine (tT 3 ), free T 3 , total thyroxine (tT 4 ) or free T 4 , suggesting that the hypothalamic-pituitary-thyroid axis is not suppressed, but rather maintained during fasting. Mean mRNA expression of adipose DI1 and DI2 increased threefold and fourfold, respectively, and 20-and 30-fold, respectively, in muscle. With the exception of adipose DI1, protein expression of adipose DI2 and muscle DI1 and DI2 increased twofold to fourfold. Fasting also increased adipose (fivefold) and muscle (fourfold) THrβ-1 mRNA expression, suggesting that the mechanisms mediating cellular TH activity are upregulated with prolonged fasting. The data demonstrate a unique, atypical mechanism of TH activity and regulation in mammals adapted to prolonged food deprivation in which the potential responsiveness of peripheral tissues and cellular TH activity are increased, which may contribute to their lipid-based metabolism.Key words: lipid metabolism, reverse T3, seal, thyroxine, triiodothyronine. THE JOURNAL OF EXPERIMENTAL BIOLOGY 4648 concentration in hibernating ground squirrels results from reduced TH metabolism, accompanied by a reduction in nuclear receptors, suggesting that TH function is suppressed despite the increase in circulating levels (i.e. cryptically hyperthyroid) (Magnus and Henderson, 1988a;Magnus and Henderson, 1988b). Such variability in the regulation of TH levels and function in food-deprived mammals demonstrates the diversity of TH physiology during periods of acute or chronic food deprivation, and highlights the necessity to perform more comprehensive studies into the functional relevance of these differences.Northern elephant seals, Mirounga angustirostris (Gill 1866), naturally fast from food and water for up to 3 months while on land (Ortiz et al., 1978; Crocker et al., 1998;Le Boeuf and Laws, 1994), and during the post-weaning fast, oxidation of non-esterified fatty acids (NEFAs) accounts for approximately 95% of the pup's metabolic rate (Ortiz et al., 1978;Viscarra et al., 2012). The fasting metabolism of seals is primarily dependent on lipid oxidation (Crocker et al., 1998;Pramfalk et al., 2011; Crocker et al., 2012a; Crocker et al., 2012...
SUMMARYFood deprivation in mammals is typically associated with reduced thyroid hormone (TH) concentrations and deiodinase content and activity to suppress metabolism. However, in prolonged-fasted, metabolically active elephant seal pups, TH levels are maintained, if not elevated. The functional relevance of this apparent paradox is unknown and demonstrates variability in the regulation of TH levels, metabolism and function in food-deprived mammals. To address our hypothesis that cellular TH-mediated activity is upregulated with fasting duration, we quantified the mRNA expression and protein content of adipose and muscle deiodinase type I (DI1) and type II (DI2), and TH receptor beta-1 (THrβ-1) after 1, 3 and 7 weeks of fasting in northern elephant seal pups (N=5-7 per week). Fasting did not decrease the concentrations of plasma thyroid stimulating hormone, total triiodothyronine (tT 3 ), free T 3 , total thyroxine (tT 4 ) or free T 4 , suggesting that the hypothalamic-pituitary-thyroid axis is not suppressed, but rather maintained during fasting. Mean mRNA expression of adipose DI1 and DI2 increased threefold and fourfold, respectively, and 20-and 30-fold, respectively, in muscle. With the exception of adipose DI1, protein expression of adipose DI2 and muscle DI1 and DI2 increased twofold to fourfold. Fasting also increased adipose (fivefold) and muscle (fourfold) THrβ-1 mRNA expression, suggesting that the mechanisms mediating cellular TH activity are upregulated with prolonged fasting. The data demonstrate a unique, atypical mechanism of TH activity and regulation in mammals adapted to prolonged food deprivation in which the potential responsiveness of peripheral tissues and cellular TH activity are increased, which may contribute to their lipid-based metabolism.Key words: lipid metabolism, reverse T3, seal, thyroxine, triiodothyronine. THE JOURNAL OF EXPERIMENTAL BIOLOGY 4648 concentration in hibernating ground squirrels results from reduced TH metabolism, accompanied by a reduction in nuclear receptors, suggesting that TH function is suppressed despite the increase in circulating levels (i.e. cryptically hyperthyroid) (Magnus and Henderson, 1988a;Magnus and Henderson, 1988b). Such variability in the regulation of TH levels and function in food-deprived mammals demonstrates the diversity of TH physiology during periods of acute or chronic food deprivation, and highlights the necessity to perform more comprehensive studies into the functional relevance of these differences.Northern elephant seals, Mirounga angustirostris (Gill 1866), naturally fast from food and water for up to 3 months while on land (Ortiz et al., 1978; Crocker et al., 1998;Le Boeuf and Laws, 1994), and during the post-weaning fast, oxidation of non-esterified fatty acids (NEFAs) accounts for approximately 95% of the pup's metabolic rate (Ortiz et al., 1978;Viscarra et al., 2012). The fasting metabolism of seals is primarily dependent on lipid oxidation (Crocker et al., 1998;Pramfalk et al., 2011; Crocker et al., 2012a; Crocker et al., 2012...
Fasting typically suppresses thyroid hormone (TH)‐mediated cellular events and increases sirtuin 1 (SIRT1) activity. THs may regulate metabolism through nongenomic pathways and directly through activation of adenosine monophosphate‐activated protein kinase (AMPK). Adult male elephant seals (Mirounga angustirostris) are active, hypermetabolic, and normothermic during their annual breeding fast, which is characterized by stable TH levels. However, the contribution of TH to maintenance of their fasting metabolism is unknown. To investigate the fasting effects on cellular TH‐mediated events and its potential association with SIRT1 and AMPK, we quantified plasma TH levels, mRNA expressions of muscle SIRT1 and TH‐associated genes as well as the phosphorylation of AMPK in adult, male northern elephant seals (n = 10/fasting period) over 8 weeks of fasting (early vs. late). Deiodinase type I (DI1) expression increased twofold with fasting duration suggesting that the potential for TH‐mediated cellular signaling is increased. AMPK phosphorylation increased 61 ± 21% with fasting suggesting that cellular metabolism is increased. The mRNA expression of the TH transporter, monocarboxylate transporter 10 (MCT10), increased 2.4‐fold and the TH receptor (THrβ‐1) decreased 30‐fold suggesting that cellular uptake of T4 is increased, but its subsequent cellular effects such as activation of AMPK are likely nongenomic. The up‐regulation of SIRT1 mRNA expression (2.6‐fold) likely contributes to the nongenomic activation of AMPK by TH, which may be necessary to maintain the expression of PGC‐1α. These coordinated changes likely contribute to the up‐regulation of mitochondrial metabolism to support the energetic demands associated with prolonged fasting in adult seals.
Thyroid hormones play an important role in the regulation of lipid metabolism. Subclinical hypothyroidism is defined as a slight increase in thyroid-stimulating hormone (TSH) with normal levels of thyroxine (T4). Hypothyroidism could be associated with altered lipid panels. This study aimed at evaluating the association between hypothyroidism and altered lipid profile. Data of 54 patients with subclinical hypothyroidism and 54 healthy individuals were collected from SBMCH laboratory. The participants belong to the age group of 20-50 years. Patients with TSH in the range of 4.2 to 10 mU/L, and T4 in the range 0.8 to 2.8 ng/dL were ruled out as hypothyroid. Control had a normal TSH ranging from 0.5 to 4.2 mU/L. The total serum cholesterol (TC), high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, and triglyceride (TG) levels were examined in both groups and the results were recorded. Participants with hypothyroidism had significantly higher LDL and lower HDL levels than the control group irrespective of age group and gender (P-value <0.001), but no difference in TG and TC levels (P-value <0.05) were observed. The prevalence of dyslipidemia and hypothyroidism was only significant in females (P-value =0.009). There was significant correlation between the prevalence of dyslipidemia and hypothyroidism regardless of gender (P-value =0.04). Hypothyroidism is associated with dyslipidemia, and biochemical screening for dyslipidemia is recommended in all patients with subclinical hypothyroidism.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.