Taiy Chemical
TRH, Thyroliberin
Synonym TRH, Thyrotropin-releasing hormone
Species Human
Protein Accession P20396
Purity Greater than 98%
Endotoxin Level < 1.0 EU per 1 μg of the protein
Biological Activity Fully biologically active when compared to a standard. The ED50 as determined by inducing prolactin secretion in rat pituitary cells is less than 3 ng/ml, corresponding to a specific activity of > 3.3 × 10^5 IU/mg.
Expression System E. coli
Fusion Tag None
Predicted Molecular Mass 3600 Da
Formulation Lyophilized from a 0.2 μm filtered solution of 20 mM Tris, 50 mM NaCl, pH 8.0
Reconstitution It is recommended to reconstitute the lyophilized TRH in sterile 18MΩ-cm H2O not less than 100 µg/ml, which can then be further diluted to other aqueous solutions.
Storage & Stability Store lyophilized TRH at -20°C. Aliquot the product after reconstitution to avoid repeated freezing/thawing cycles. Reconstituted TRH can be stored at 4°C for a limited period of time.
FAQ
What is TRH, Thyroliberin, and what role does it play in the endocrine system?

Thyrotropin-releasing hormone (TRH), also known as thyroliberin, is a pivotal hypothalamic hormone that serves as the primary regulator of thyroid-stimulating hormone (TSH) secretion by the anterior pituitary gland. TRH is a tripeptide hormone, meaning it consists of three amino acids, and it is synthesized in the neurons of the hypothalamus. It plays an integral role in the hypothalamus-pituitary-thyroid (HPT) axis, which is crucial for maintaining the body's metabolic homeostasis. Once TRH is released into the hypothalamic-pituitary portal circulation, it travels to the anterior pituitary gland, where it binds to the TRH receptor on the surface of thyrotroph cells. This binding action stimulates the cells to secrete TSH into the bloodstream.

TSH is responsible for prompting the thyroid gland to produce and release thyroid hormones, primarily thyroxine (T4) and triiodothyronine (T3). These hormones regulate various aspects of metabolism, such as energy utilization, heat production, and protein synthesis, making TRH an essential factor in overall metabolic regulation. Beyond stimulating TSH production, TRH also influences the release of prolactin, another pituitary hormone, though this is a minor role compared to its impact on TSH secretion.

In addition to its endocrine functions, TRH is recognized for its neuromodulatory effects in the central nervous system. It influences specific neurological pathways, contributing to mood regulation, nociception, and thermoregulation. This underscores the multifaceted nature of TRH, highlighting its importance beyond the traditional view of a solely endocrine regulator. Understanding TRH's functions and mechanisms provides insight into the complexities of endocrine and neurological interconnections, prompting further research into its therapeutic potentials for disorders like hypothyroidism, depression, and neurodegenerative diseases.

What are the therapeutic applications of TRH, Thyroliberin, in modern medicine?

Thyrotropin-releasing hormone (TRH), also known by its alternative name thyroliberin, has garnered interest in the medical field for its potential therapeutic applications, stemming from its role in regulating the hypothalamus-pituitary-thyroid (HPT) axis and its neuromodulatory effects. One primary area of exploration is in the treatment of hypothyroidism, particularly central or secondary hypothyroidism caused by inadequate stimulation of the thyroid gland due to insufficient TSH production by the pituitary gland. As TRH stimulates TSH production, administering TRH might offer a direct method to increase TSH levels and, consequently, thyroid hormone production in affected individuals.

However, the therapeutic applications of TRH extend beyond thyroid disorders. Due to its neuromodulatory effects, TRH has been investigated for its potential in treating neurodegenerative diseases and mood disorders. Research has suggested that TRH could exert neuroprotective effects and improve motor function, making it an area of interest in conditions like amyotrophic lateral sclerosis (ALS) and spinocerebellar degeneration. Furthermore, TRH may possess antidepressant properties, with studies indicating its potential effectiveness in treating refractory depression; it may help modulate mood by influencing neurotransmitter release and neuronal excitability.

Additionally, TRH's ability to influence neurotransmission and neuroendocrine responses illuminates its potential to address various neurological and psychiatric conditions. Its role in enhancing arousal and mitigating fatigue could be leveraged in treating conditions characterized by excessive somnolence or lack of motivation. As research progresses, the understanding of TRH's mechanisms will likely expand, potentially leading to its integration into therapeutic approaches for a broader range of health issues.

However, while the therapeutic possibilities are promising, there are challenges related to the systemic administration of TRH, including its rapid degradation in the bloodstream. Consequently, the development of analogs or delivery methods that increase its stability and bioavailability is crucial for translating the therapeutic potential of TRH into practical medical applications.

How does TRH, Thyroliberin, impact neurological function and behavior?

Thyrotropin-releasing hormone (TRH), commonly referred to as thyroliberin, is traditionally recognized for its role in the endocrine system, particularly regarding the regulation of the hypothalamus-pituitary-thyroid (HPT) axis. However, its influence extends significantly into the central nervous system (CNS), where it acts as a neuromodulator with profound effects on neurological function and behavior. TRH's involvement in the CNS is facilitated through widespread distribution across various brain regions, including the spinal cord, cerebellum, and limbic system, which are involved in motor control, emotional processing, and autonomic functions.

TRH has been implicated in mood regulation, largely due to its ability to interact with neurotransmitter systems like serotonin, dopamine, and acetylcholine. It enhances catecholamine release, which contributes to its potential antidepressant effects. This neuromodulatory role makes TRH relevant in research focused on mood disorders, including depression, where traditional treatments may be inadequate. In clinical settings, TRH has been shown to evoke arousal and alertness, suggesting potential applications in treating disorders marked by excessive sleepiness or lack of motivation.

Additionally, TRH influences the body's response to stress and has been found to impact the hypothalamic-pituitary-adrenal (HPA) axis, which regulates the stress response. By modulating the release of corticotropin-releasing hormone (CRH) and subsequently affecting cortisol levels, TRH can influence how the body copes with stress, highlighting its relevance in understanding stress-related disorders. Beyond mood and stress, TRH has been studied for its neuroprotective properties. Research suggests it can enhance neuronal survival, potentially offering therapeutic benefits in neurodegenerative diseases like Alzheimer's and Parkinson's diseases, where it may mitigate neuronal death and improve cognitive functions.

Moreover, TRH impacts thermoregulation, nociception, and food intake, indicating a broad spectrum of influence over physiological processes. Its ability to reduce pain perception and regulate body temperature showcases its multifaceted contributions to maintaining homeostasis. As the complexities of TRH’s roles in the CNS continue to unravel, it becomes increasingly apparent that TRH holds promise not only as a hormonal regulator but also as a pivotal player in maintaining neurological and behavioral equilibrium.

What are the effects of TRH, Thyroliberin, on metabolism and energy balance?

Thyrotropin-releasing hormone (TRH), also referred to as thyroliberin, is a crucial component of the hypothalamus-pituitary-thyroid (HPT) axis, which plays a significant role in regulating metabolism and energy balance within the body. TRH is synthesized in the hypothalamus and stimulates the anterior pituitary gland to release thyroid-stimulating hormone (TSH). In turn, TSH promotes the thyroid gland to produce thyroid hormones, primarily thyroxine (T4) and triiodothyronine (T3). These hormones are integral to maintaining metabolic rate and energy balance, highlighting the pivotal role of TRH in these processes.

Thyroid hormones influence the basal metabolic rate (BMR), which refers to the amount of energy expended while at rest. They modulate the expression of genes involved in energy metabolism, enhance mitochondrial activity, and regulate the metabolism of carbohydrates, proteins, and fats. By controlling these metabolic pathways, TRH indirectly influences how the body uses and stores energy. An increase in thyroid hormone levels, stimulated by TRH, typically leads to enhanced metabolism, increased energy expenditure, and weight loss, while a deficiency results in the opposite effects.

Moreover, TRH has a direct impact on appetite and feeding behavior. Research has indicated that TRH can modulate the release of appetite-regulating neuropeptides and neurotransmitters within the hypothalamus, affecting feeding behavior and energy intake. It also interacts with other hormones such as leptin and ghrelin, which are crucial for hunger regulation and energy balance. The complex interplay between TRH and these regulatory systems ensures that the body maintains energy homeostasis, adapting to the varying demands of the environment.

In addition to its metabolic effects, TRH influences thermogenesis, the process of heat production in organisms. Thermogenesis plays a vital role in managing body temperature and energy expenditure, especially in response to cold environments or during periods of overfeeding. By influencing thyroid hormone levels, TRH indirectly promotes adaptive thermogenesis, which is essential for maintaining body temperature and metabolic health.

As research progresses, understanding the direct and indirect effects of TRH on metabolism opens doors for potential therapeutic interventions to address metabolic disorders such as obesity, metabolic syndrome, and hypothyroidism. By manipulating the TRH-signalling pathway, it may be possible to develop treatments that effectively modulate energy expenditure and improve metabolic health.

Can TRH, Thyroliberin, be used as a diagnostic tool in evaluating thyroid function?

Thyrotropin-releasing hormone (TRH), or thyroliberin, is a fundamental hypothalamic hormone involved in controlling the secretion of thyroid-stimulating hormone (TSH) from the anterior pituitary gland. Given its pivotal role in regulating thyroid function via the hypothalamus-pituitary-thyroid (HPT) axis, TRH has been explored as a diagnostic tool in evaluating thyroid function, particularly through the TRH stimulation test. This test was traditionally used to assess the functional responsiveness of the pituitary gland and differentiate between various forms of hypothyroidism and hyperthyroidism.

In a TRH stimulation test, TRH is administered intravenously, prompting the anterior pituitary to release TSH, which can subsequently be measured to assess pituitary function. In a healthy individual, this should lead to a noticeable increase in TSH levels, as the pituitary responds to the TRH stimulus. The test is particularly insightful for evaluating patients with secondary (pituitary) or tertiary (hypothalamic) hypothyroidism. In secondary hypothyroidism, the pituitary gland's response is typically blunted or absent because the gland itself is malfunctioning. In tertiary hypothyroidism, where the defect lies in the hypothalamus, the pituitary gland usually shows a normal or exaggerated response due to prolonged underexposure to TRH.

Moreover, the TRH test has been utilized in diagnosing hyperthyroidism, especially in distinguishing between primary hyperthyroidism and inappropriate TSH secretion by evaluating the pituitary's responsiveness to TRH. In primary hyperthyroidism, where the thyroid gland is overactive, the pituitary response to TRH is often reduced due to negative feedback from elevated thyroid hormones. Although the advent of more sophisticated hormone assays and imaging techniques has relegated the TRH stimulation test to a secondary role, it remains a useful diagnostic tool in specific contexts where standard tests yield inconclusive results.

Despite its diagnostic potential, the TRH stimulation test has limitations, such as variability in TRH response among individuals and potential adverse reactions to TRH administration. As a result, it is not routinely used in modern thyroid function evaluation, with reliance primarily placed on serum TSH, free T4, and free T3 measurements. Nonetheless, in cases of central hypothyroidism or complex endocrine disorders, the TRH stimulation test may still provide valuable insight into pituitary and hypothalamic function. As endocrinological research evolves, integrating TRH testing with advanced diagnostic methods may enhance our understanding and management of thyroid-related conditions.

How does TRH, Thyroliberin, influence prolactin secretion, and what are its implications?

Thyrotropin-releasing hormone (TRH), also known as thyroliberin, is primarily recognized for its role in regulating the thyroid-stimulating hormone (TSH) secretion from the anterior pituitary gland. However, TRH also exerts a significant influence on the secretion of prolactin, another hormone produced by the anterior pituitary. Prolactin plays a crucial role in lactation, reproductive functioning, and immune system regulation. The relationship between TRH and prolactin secretion highlights the intricate interplay within the endocrine system, suggesting broader implications for physiological processes and potential therapeutic applications.

The mechanism by which TRH influences prolactin secretion involves its action on the anterior pituitary cells, known as lactotrophs. Upon TRH binding to its receptor on these cells, signaling pathways are activated that lead to increased prolactin gene expression and secretion. This effect is particularly evident during conditions where physiological demands for prolactin are high, such as pregnancy and lactation, when TRH can enhance prolactin release to facilitate mammary gland development and milk production.

Furthermore, the effect of TRH on prolactin secretion underscores its involvement in reproductive health. Prolactin has an inhibitory effect on the reproductive axis by suppressing gonadotropin-releasing hormone (GnRH) secretion and thus reducing luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels. This can have clinical implications, such as in prolactinoma, a condition characterized by excessive prolactin production leading to reproductive dysfunctions like amenorrhea, infertility, and galactorrhea. Understanding TRH's role in prolactin regulation can aid in the therapeutic management of such conditions by modulating TRH activity to normalize prolactin levels.

Moreover, the interaction between TRH and prolactin is of interest in psychiatric research, particularly concerning the hormone's role in behavior and emotional regulation. Prolactin has been implicated in stress response and mood regulation, suggesting that TRH's influence on prolactin secretion might contribute to neuropsychological processes. This relationship offers potential avenues for exploring new treatments for mood disorders, as altering TRH or prolactin levels could have therapeutic effects.

While the physiological and clinical relevance of TRH's modulation of prolactin is established, the intricate details of these mechanisms warrant further exploration. As research in endocrinology advances, understanding TRH's influence on prolactin secretion can lead to novel insights into managing various reproductive, metabolic, and psychological disorders by harnessing the modulatory capabilities of TRH within the endocrine system.
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