Taiy Chemical
PTH (1-31) Amide (human)
Synonym pTH (1-31) amide (human)
Species Human
Protein Accession N/A
Purity Greater than 95%
Endotoxin Level Less than 0.1 ng/µg
Biological Activity N/A
Expression System Chemical synthesis
Fusion Tag N/A
Predicted Molecular Mass N/A
Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA
Reconstitution It is recommended to reconstitute the lyophilized pTH (1-31) in sterile 18MΩ-cm H2O not less than 100μg/ml, which can then be further diluted to other aqueous solutions.
Storage & Stability Lyophilized pTH (1-31) although stable at room temperature for 3 weeks, should be stored desiccated below -18°C.
FAQ
What is pTH (1-31) amide (human), and what role does it play in human health?

Parathyroid hormone (PTH) is a critical regulator of calcium and phosphate metabolism in the body. Produced by the parathyroid glands, it plays a pivotal role in maintaining serum calcium levels within a narrow physiological range. The pTH (1-31) amide is a peptide fragment of the full-length PTH molecule, specifically consisting of the first 31 amino acids modified at the C-terminus to include an amide group. This modification is significant because the N-terminal region of PTH is primarily responsible for its biological activity, meaning that pTH (1-31) amide retains many of the skeletal effects of the full-length hormone.

In human health, PTH's primary actions are on the bones, kidneys, and, indirectly, the intestines. It stimulates osteoclasts in the bones to increase bone resorption, releasing calcium and phosphate into the bloodstream. In the kidneys, PTH increases calcium reabsorption in the distal tubules while promoting phosphate excretion. This finely tuned balance is crucial for various physiological processes, including nerve conduction, muscle contraction, and blood coagulation. Additionally, PTH facilitates the conversion of vitamin D to its active form in the kidneys, which then enhances intestinal absorption of calcium and phosphate.

Understanding the specific role of pTH (1-31) amide involves appreciating its potential therapeutic implications. As a potent fragment of PTH, it could provide benefits in conditions where bone health is compromised. For instance, osteoporosis, a condition characterized by bone density loss and increased fracture risk, could be managed more effectively with treatments targeting bone regeneration and reducing further bone resorption. The action of pTH (1-31) amide, with its ability to stimulate bone formation without the simultaneous catabolic effects, is a promising area for research and therapeutic development. Thus, dissecting the role of this peptide in human health not only enhances our understanding of PTH’s broader biological functions but also points toward innovative treatments for metabolic bone diseases.

How is pTH (1-31) amide (human) used in medical research?

In medical research, pTH (1-31) amide (human) serves as a powerful tool for exploring various aspects of bone biology and calcium homeostasis. Its specific configuration makes it an interesting candidate for studying PTH’s primary functions independent of its full-length counterpart. The pTH (1-31) amide is often employed to examine the anabolic effects of PTH on bone formation, distinct from its resorptive activities, which are appreciated in the context of managing osteoporosis and other bone degenerative diseases. Researchers are particularly interested in this fragment due to its capacity to promote osteoblastic activity, leading to new bone matrix formation.

One area where pTH (1-31) amide is profoundly impactful is in the development of new osteoporosis treatments. Traditional therapies often focus on inhibiting bone resorption, which, while beneficial, do not address the deficit in bone formation. The ability of pTH (1-31) amide to stimulate osteoblasts and enhance bone mass represents a paradigm shift toward anabolic treatment strategies that not only halt bone loss but actively rebuild bone. This is crucial for developing therapeutics that can improve bone density and structural integrity more holistically.

Moreover, pTH (1-31) amide is also used to delineate the mechanisms of PTH receptor interactions. The understanding of ligand-receptor dynamics is fundamental for the design of receptor-selective drugs that can maximize therapeutic benefits while minimizing side effects. These insights are critical, especially for patients who might be sensitive to the hypercalcemic effects of full-length PTH treatments, by selectively activating pathways that enhance bone formation without eliciting significant hypercalcemia.

In addition to these areas, the use of pTH (1-31) amide in research extends to evaluating its potential in addressing hypoparathyroid conditions. Here, maintaining an anabolic environment without excessive calcium mobilization can significantly enhance patient outcomes. With ongoing research, the nuanced understanding provided by studies involving pTH (1-31) amide continues to propel forward the possibilities for tailored, effective treatments in endocrinology and bone health.

What are the potential benefits of pTH (1-31) amide (human) in treating osteoporosis?

Osteoporosis is a prevalent bone disease characterized by decreased bone mass and structural deterioration, increasing fracture risk. Traditional treatment modalities primarily focus on inhibiting bone resorption; however, these approaches do not facilitate new bone formation, a necessary component for restoring bone health in osteoporotic patients. Here is where pTH (1-31) amide (human) shows promise. This peptide fragment holds the potential for a fundamentally different treatment approach—an anabolic therapy that encourages new bone growth, providing a substantial benefit over existing therapies.

The mechanism by which pTH (1-31) amide exerts its beneficial effects primarily involves stimulating osteoblast activity. Osteoblasts are the cells responsible for bone formation, synthesizing new bone matrix, and facilitating mineralization. By actively promoting osteoblastic function, pTH (1-31) amide can help rebuild bone architecture, thereby increasing bone mass and strength. This not only counteracts the bone loss associated with osteoporosis but also fortifies skeletal integrity, reducing the likelihood of fractures, which are a significant concern.

Furthermore, clinical research suggests that pTH (1-31) amide has a dual role of stimulating bone formation without proportionately increasing bone resorption, as seen with full-length PTH or other anabolic treatments. This selective stimulation is particularly critical for patients who need bone density improvement without experiencing adverse hypercalcemic side effects. By providing an improved safety profile, pTH (1-31) amide stands out as a potential therapy, especially for patients with underlying conditions that may predispose them to calcium metabolism disorders.

Additionally, the benefit of using pTH (1-31) amide in treating osteoporosis extends to potential improvements in bone quality. Beyond mere increases in bone mineral density (BMD), enhancing the quality of bone microarchitecture and the toughness of bone are essential for reducing fracture risks. The peptide’s influence on collagen arrangement and mineral distribution in the bone matrix could markedly improve these quality parameters, leading to more significant clinical outcomes than those achievable by simply mitigating bone loss.

These multifaceted benefits underscore the transformative potential of pTH (1-31) amide as part of osteoporosis management. With its focus on bone building rather than merely slowing bone breakdown, it aligns with therapeutic goals aimed at restoring natural bone strength and durability, offering hope for improved quality of life for individuals at risk for or suffering from osteoporosis.

How does pTH (1-31) amide (human) differ from other parathyroid hormone treatments?

The pTH (1-31) amide (human) differs from other parathyroid hormone treatments in several critical ways that pertain to its structure, mechanism of action, and therapeutic effects, particularly in the context of bone health management. At the structural level, pTH (1-31) amide represents a truncated form of the full parathyroid hormone, consisting of the first 31 amino acids of the polypeptide, modified at the C-terminus to form an amide. These modifications provide it the ability to act selectively within the body, targeting specific receptor-mediated pathways that provide its therapeutic effect.

Full-length PTH or other extended forms of the hormone usually stimulate both anabolic and catabolic pathways. While beneficial for enhancing bone formation, this dual action often results in increased bone resorption as well, which can lead to a less-than-ideal therapeutic profile for certain patients. Conversely, pTH (1-31) amide’s shorter structure and targeted receptor interactions predominantly stimulate osteoblastic activity without a commensurate increase in osteoclastic activity. This results in a net anabolic effect—more bone formation—as opposed to a simultaneous stimulation of bone resorption that might counteract gains in bone density.

From a pharmacodynamic perspective, this selective action is highly desirable in patients where bone density preservation and increase are critical, such as those with osteoporosis. This makes pTH (1-31) amide an attractive candidate for developing therapeutics aimed at enhancing bone mass and structural integrity while minimizing adverse effects such as hypercalcemia, a common concern in treatments involving longer forms of parathyroid hormone or its analogs.

The differences extend to administration strategies and patient compliance as well. The selective and targeted nature of pTH (1-31) amide could potentially translate into dosing advantages, where lower doses achieve the desired outcome, improving patient adherence by reducing complexity in treatment regimens. This is vital in long-term management scenarios, where consistent therapeutic engagement is crucial for success.

Such distinct characteristics of pTH (1-31) amide not only differentiate it from other forms of parathyroid hormone treatments but also open new avenues for its application beyond where traditional PTH analogs are employed. It highlights the peptide's potential for broader use in treating various metabolic or degenerative bone conditions, providing a novel approach that leverages its unique mechanism, efficacy, and safety profile.

What are the safety considerations associated with using pTH (1-31) amide (human)?

When considering the use of pTH (1-31) amide (human) for therapeutic applications, understanding its safety profile is of paramount importance. One of the notable advantages of this peptide is its selective mechanism of action. Because it predominantly stimulates bone formation without significantly increasing bone resorption, the risk of hypercalcemia—a common side effect associated with general PTH therapies—is reduced. Hypercalcemia can cause various symptoms and complications, such as muscular weakness, fatigue, and in severe cases, cardiac arrhythmias. Therefore, the reduced impact on calcium mobilization is a significant safety benefit of pTH (1-31) amide.

However, as with any hormonal treatment, potential risks need to be carefully monitored. The administration of hormones or hormone-like substances can have systemic effects, where unintended stimulation of pathways can occur. For pTH (1-31) amide, while the risk is minimized compared to full-length PTH treatments, vigilance in monitoring patients for signs of hypercalcemia is still warranted, particularly in those with underlying health conditions affecting calcium metabolism or renal function.

Moreover, long-term use of anabolic agents, even those selective for osteoblasts, requires consideration given the delicate balance of bone remodeling processes. Excessive promotion of bone formation without matched resorption can, in some cases, lead to aberrant bone growth or alterations in bone quality. These concerns necessitate ongoing research and careful clinical planning, including periodic bone density assessments to ensure balanced bone turnover is maintained.

Patient-specific factors also play a crucial role in determining the safety and efficacy of pTH (1-31) amide treatments. Medical history, concurrent medications, and pre-existing conditions all influence therapeutic decisions. For instance, patients with severe kidney disease may face challenges related to calcium handling, necessitating tailored approaches to treatment and more rigorous monitoring of physiological responses to pTH (1-31) amide.

Finally, potential allergic reactions and injection site reactions are standard safety considerations for any peptide-based treatment administered subcutaneously. While such occurrences are generally rare and mild, they must be accounted for when planning a patient’s treatment regimen. Educating patients about the signs of adverse reactions and regularly reviewing their condition during follow-up appointments is essential to managing such risks effectively.

Thus, while pTH (1-31) amide presents a favorable safety profile due to its targeted action, comprehensive screening, and careful monitoring during treatment, it remains essential to minimize risks and maximize clinical benefits.
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