Publications by authors named "Alice Batistuzzo"

Article Synopsis
  • About half of the global population carries the Ala92-DIO2 allele, which can reduce the effectiveness of the enzyme that converts T4 to T3, affecting metabolism.
  • Research using two types of mice (C57Bl/6J and FVB/N) found that the metabolic effects of the Ala92-Dio2 allele vary significantly, with FVB mice showing notable issues like hypercholesterolemia and liver fat accumulation, while B6 mice did not exhibit these problems.
  • The study highlights that the genetic background influences how the Ala92-DIO2 allele impacts metabolism, suggesting future clinical trials should consider this variability to understand why previous studies have shown mixed results across different populations.
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The regulation of thyroid activity and thyroid hormone (TH) secretion is based on feedback mechanisms that involve the anterior pituitary TSH and medial basal hypothalamus TSH-releasing hormone. Plasma T3 levels can be "sensed" directly by the anterior pituitary and medial basal hypothalamus; plasma T4 levels require local conversion of T4 to T3, which is mediated by the type 2 deiodinase (D2). To study D2-mediated T4 to T3 conversion and T3 production in the anterior pituitary gland, we used mouse pituitary explants incubated with 125I-T4 for 48 hours to measure T3 production at different concentrations of free T4.

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Norepinephrine plays an important role in modulating memory through its beta-adrenergic receptors (Adrβ: β, β and β). Here, we hypothesized that multisensory stimulation would reverse memory impairment caused by the inactivation of Adrβ (AdrβKO) with consequent inhibition of sustained glial-mediated inflammation. To test this, 21- and 86-day-old AdrβKO mice were exposed to an 8-week multisensory stimulation (MS) protocol that comprised gustatory and olfactory stimuli of positive and negative valence; intellectual challenges to reach food; the use of hidden objects; and the presentation of food in ways that prompted foraging, which was followed by analysis of GFAP, Iba-1 and EAAT2 protein expression in the hippocampus (HC) and amygdala (AMY).

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Gestational hypothyroidism can impair development, cognition, and mood. Here, we tested whether multisensory stimulation (MS) improves the phenotype of rats born to surgically thyroidectomized (Tx) dams suboptimally treated with LT4. 8-week-old female Tx Wistar rats were kept on daily LT4 (0.

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The Thr92Ala-Dio2 polymorphism has been associated with reduced cognition in 2-month-old male mice and increased risk for cognitive impairment and Alzheimer's disease in African Americans. This has been attributed to reduced thyroid hormone (TH) signaling and endoplasmic reticulum (ER) stress in the brain. Here we studied the Thr92Ala-Dio2 mouse model and saw that older male mice (7-8-month-old) exhibited a more severe cognition impairment, which extended to different aspects of declarative and working memories.

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Objective: Patient-centered studies have shown that several patients on thyroid hormone replacement therapy for hypothyroidism exhibit persistent symptoms, including "brain fog." Here, we aimed to determine which of these specific symptoms are associated with brain fog, identify patient-reported factors that modify these symptoms, and identify patient concerns related to brain fog not included in thyroid-specific questionnaires.

Methods: A survey on brain fog symptoms adapted from thyroid-specific patient-reported outcome was distributed online.

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Clinical and subclinical hypothyroidism are the most common hormonal dysfunctions during pregnancy. Insufficient maternal thyroid hormones (THs) in the early stages of pregnancy can lead to severe impairments in the development of the central nervous system because THs are critical to central nervous system development. In the fetus and after birth, THs participate in neurogenic processes, cell differentiation, neuronal activation, axonal growth, dendritic arborization, synaptogenesis and myelination.

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