Thyroxine Metabolism

Thyroxine metabolism is the set of processes that produce, transport, activate, and clear thyroxine (T4), a thyroid hormone that helps regulate energy use, development, and nervous-system function. In peripheral tissues, deiodinase enzymes remove iodine atoms from T4 to form the more active triiodothyronine (T3) or inactive reverse T3, while the hypothalamic-pituitary-thyroid axis adjusts secretion through negative feedback. In psychology and behavioral research, these pathways matter because altered thyroid hormone availability can affect brain development, mood, attention, and cognition, helping researchers interpret behavioral symptoms and investigate links between endocrine function and mental health.

Thyroxine Metabolism - Related Videos

Education

JoVE Core - Biology

What is Metabolism?

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2019

Overview Metabolism represents all of the chemical activity in a cell, including reactions that build molecules (anabolism) and those that break molecules down (catabolism). Anabolic reactions require energy, whereas catabolic reactions provide it. Thus, metabolism describes how cells transform energy through a variety of chemical reactions, which are often made more efficient with the help of enzymes. Metabolism Is the Sum of All of the Chemical Reactions That Take Place in an Organism

Research

JoVE Journal - Biology
Free Sample

Non-chromatographic Purification of Recombinant Elastin-like Polypeptides and their Fusions with Peptides and Proteins from Escherichia coli

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Cited by 48 •

2014

Elastin-like polypeptides are stimulus-responsive biopolymers with applications ranging from recombinant protein purification to drug delivery. This protocol describes the purification and characterization of elastin-like polypeptides and their peptide or protein fusions from Escherichia coli using their lower critical solution temperature phase transition behavior as a simple alternative to chromatography.

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides

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Cited by 6 •

2012

We describe here a technique that is now routinely used to isolate stably bound ribosome nascent chain complexes (RNCs). This technique takes advantage of the discovery that a 17 amino acid long SecM "arrest sequence" can halt translation elongation in a prokaryotic (E. coli) system, when inserted into (or fused to the C-terminus) of virtually any protein.

Isolation of Ribosome Bound Nascent Polypeptides in vitro to Identify Translational Pause Sites Along mRNA

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Cited by 2 •

2012

A technique to identify translational pause sites on mRNA is described. This procedure is based on isolation of nascent polypeptides accumulating on ribosomes during in vitro translation of a target mRNA, followed by the size analysis of the nascent chains using a denaturing gel electrophoresis.

Research

JoVE Journal - Biology
Free Sample

Metabolic Profile Analysis of Zebrafish Embryos

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Cited by 42 •

2013

Zebrafish represent a powerful vertebrate model that has been under-utilised for metabolic studies. Here we describe a rapid way to measure the in vivo metabolic profile of developing zebrafish that allows the comparison of different mitochondrial function parameters between genetically or pharmacologically manipulated embryos, thereby increasing the applicability of this organism.

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