Taiy Chemical
PTH (28-48) (human)
Synonym parathyroid hormone (28-48)
Species Human
Protein Accession P01270
Purity >95%
Endotoxin Level <1.0 EU per μg
Biological Activity The ED50 is 2-8 ng/mL
Expression System E. coli
Fusion Tag None
Predicted Molecular Mass 2353 Da
Formulation Lyophilized from a 0.2 μm filtered solution in PBS
Reconstitution Reconstitute in water to a concentration of 0.1-1.0 mg/mL
Storage & Stability Store at -20°C. For long-term storage, store at -80°C. Avoid repeated freeze-thaw cycles.
FAQ
What is pTH (28-48) (human), and how does it differ from other parathyroid hormone treatments?

pTH (28-48) (human) is a specialized fragment of the human parathyroid hormone, specifically targeting the amino acid sequence from 28 to 48. This peptide stands out in the field of endocrinology because it encompasses a mid-region sequence distinct from the N-terminal or C-terminal fragments that are more commonly used in other parathyroid-related treatments. Most clinically used fragments, such as Teriparatide, are based on the N-terminal sequence, comprising the first 34 amino acids of the full-length parathyroid hormone (PTH) molecule. These treatments primarily focus on stimulating bone growth and treating osteoporosis, leveraging the potent anabolic effects of the N-terminal region. However, the mid-region fragment, pTH (28-48), offers a unique set of biological interactions that are currently being explored for their potential therapeutic benefits.

The pTH (28-48) sequence is hypothesized to engage with different receptors or protein-binding partners that might not be effectively targeted by the N-terminal or full-length hormone. This suggests a potentially distinct functional or modulatory role within the broader scope of calcium and phosphate metabolism regulation. Furthermore, preliminary studies indicate that this mid-region fragment may influence cell signaling pathways in a way that complements or differs from the action of the full-length hormone, potentially offering novel therapeutic avenues for diseases related to calcium imbalance or conditions such as hypercalcemia, hypocalcemia, and certain metabolic bone disorders.

In terms of therapeutic applications, researchers are investigating the nuanced effects of pTH (28-48) in comparison to the more prevalent forms. The focus is on understanding whether this peptide offers advantages such as reduced side effects, a different safety profile, or enhanced efficacy for specific patient populations that might not respond well to existing therapies. Additionally, pTH (28-48) might offer insights into poorly understood mechanisms of PTH action, further enriching our understanding of hormonal balance and its implications for human health.

Can pTH (28-48) (human) be used for osteoporosis treatment similar to other parathyroid hormone fragments?

While pTH (28-48) (human) represents an intriguing area of research, it is not currently employed as a direct treatment for osteoporosis like some other parathyroid hormone (PTH) fragments, such as Teriparatide, which is specifically designed from the N-terminal 1-34 sequence of the hormone. The N-terminal portion is renowned for its anabolic effects on bone, promoting osteoblast activity and increasing bone density over time. These properties make it highly effective for increasing bone mass in patients with osteoporosis, a condition characterized by weak and brittle bones.

In contrast, the mid-region fragment, pTH (28-48), is not traditionally associated with direct modulation of osteoblast activity. Its potential benefits are still the subject of ongoing research, particularly concerning its interaction with different receptors or signaling pathways compared to the N-terminal or full-length hormone. There's a growing body of exploratory work focusing on how this sequence might influence bone metabolism or other facets of calcium and phosphate homeostasis, potentially offering supplementary benefits when used in conjunction with other treatments.

Researchers are investigating whether pTH (28-48) could complement existing osteoporosis therapies by modulating aspects of calcium handling that are not addressed by traditional treatments or by offering a targeted approach to specific patient populations with unique metabolic profiles or needs. Additionally, pTH (28-48) could help shed light on the broader mechanisms of hormonal regulation that affect bone density and strength, possibly leading to the development of synergistic treatment protocols.

As scientific understanding of its role expands, it's conceivable that pTH (28-48) might be integrated into complex therapeutic regimens aimed at osteoporosis and other bone-related conditions. However, until more conclusive evidence is gathered through rigorous clinical trials, it remains primarily an object of research inquiry, and patients should rely on approved treatments under the guidance of their healthcare providers.

What are the potential benefits of using pTH (28-48) (human) in clinical settings?

The potential benefits of using pTH (28-48) (human) in clinical settings are primarily linked to its unique interaction within the body's hormonal systems, particularly in areas that remain underserved by conventional parathyroid hormone (PTH) therapies. As a distinct fragment encompassing the 28-48 amino acid sequence, it offers a promising avenue for expanding our understanding and treatment capabilities in cases involving complex calcium and phosphate homeostasis.

One of the most significant advantages hypothesized for pTH (28-48) is its possible involvement in nuanced regulatory processes that are not adequately addressed by full-length PTH or its N-terminal derivatives. This includes areas such as modulation of renal tubular reabsorption of calcium and phosphate, contributing to a more precise control of serum levels of these minerals. Such control is crucial for conditions where standard therapies do not achieve optimal balance or in cases of resistance to existing treatments.

Additionally, pTH (28-48) might offer an innovative approach for targeting specific PTH receptors or signaling pathways that could lead to localized effects without widespread systemic implications, potentially resulting in fewer side effects compared to traditional therapies. For instance, managing hypercalcemia or hypocalcemia with a targeted therapeutic peptide that limits systemic action could reduce the risk of complications such as nephrolithiasis, cardiovascular issues, or gastrointestinal disturbances.

In research contexts, pTH (28-48) is also being explored for its prospective role in elucidating the intricate network of hormonal interactions and their impact on cellular and systemic physiology. This peptide may act as a valuable tool for decoding complex endocrine pathways, contributing to both basic scientific understanding and applied clinical strategies. If proven effective, it could be part of combination therapies that incorporate its specific benefits with other PTH fragments to maximize therapeutic outcomes for metabolic bone diseases and related disorders.

Ultimately, the clinical benefits of pTH (28-48) will be determined by ongoing research, which aims to validate these hypotheses and define the scope of its application. This includes establishing its safety profile, determining optimal dosing regimens, and identifying patient populations that may benefit most from its unique properties, thus paving the way for advanced, personalized healthcare solutions.

How does pTH (28-48) (human) interact with body systems to regulate calcium levels?

The interaction of pTH (28-48) (human) with body systems to regulate calcium levels, while not as extensively documented as other parathyroid hormone (PTH) fragments, is an area of active investigation with intriguing scientific potential. The human body regulates calcium levels through a complex network involving the bones, kidneys, and gastrointestinal tract, alongside the regulatory hormone parathyroid hormone (PTH) itself.

Traditionally, PTH modulates calcium levels by increasing renal tubular calcium reabsorption, enhancing the intestinal absorption of calcium (indirectly through stimulating the activation of vitamin D), and mobilizing calcium from bones into the bloodstream. These actions are primarily driven by the N-terminal region of the hormone. However, pTH (28-48) introduces a new perspective, focusing on a mid-region fragment whose direct interaction within these systems is less conventional and is believed to be involved in fine-tuning certain aspects of calcium regulation.

In bone metabolism, the modulatory role of pTH (28-48) could involve signaling pathways that influence osteoclast and osteoblast activity differently than the N-terminal action generally associated with bone resorption and formation. Its unique interaction might provide insights into maintaining bone quality or mineralization, underscoring its potential in research areas addressing bone matrix integrity.

In the renal system, pTH (28-48) might exert a role in the nuanced regulation of calcium and phosphate reabsorption. By possibly interacting with distinct PTH receptors or influencing secondary messengers, this fragment could refine our approach to managing aberrant renal handling of calcium, thus potentially offering a targeted method for addressing hypercalciuria or hypophosphatemia.

Research into pTH (28-48) also opens up possibilities for understanding its effects on cellular pathways not traditionally associated with PTH. These might include cross-talk with other hormonal systems or intracellular feedback mechanisms that collectively influence whole-body calcium balance. Unlike the direct anabolic actions on bone or renal calcium transport seen with other PTH treatments, pTH (28-48) might participate in broader systemic regulation—impacting overall mineral balance subtly.

As scientific efforts continue to unveil the role of pTH (28-48) in calcium homeostasis, uncovering these interactions offers the promise of precise, tailored interventions for individuals whose calcium regulation does not conform to standard therapeutic approaches. Clinically, this could mean new opportunities for managing diseases marked by imbalances in calcium, thereby enhancing patient outcomes with more specialized treatment options.

Are there any known side effects or safety concerns associated with pTH (28-48) (human)?

At present, the understanding of side effects and safety concerns associated with pTH (28-48) (human) is still developing, as this peptide remains in the research phase and is not yet a standard therapeutic agent. As with any novel treatment under investigation, comprehensive safety evaluations are crucial to ensure that any potential risks are well understood and managed before clinical application.

Given the complexity of manipulating endocrine pathways and, specifically, the calcium-regulating functions of parathyroid hormone (PTH), it is vital to closely monitor how pTH (28-48) interacts with systemic physiology. The broader PTH hormone and its analogs have been associated with a variety of side effects, largely related to their ability to significantly alter calcium and phosphate metabolism. While the effects of the full hormone or its N-terminal fragments provide a reference, the distinct sequence of pTH (28-48) implies that its side effect profile could differ due to its unique interaction with receptors or intracellular signaling pathways.

Potential safety concerns involving pTH (28-48) could include hypercalcemia or hypocalcemia if calcium regulation is disrupted. The peptide’s effects on renal function might also lead to imbalances in calcium and phosphate reabsorption, potentially affecting kidney health over time. Further examination is essential to understand the peptide’s potency and specificity and to ensure its effects are confined to intended targets without broad systemic disturbances.

Another concern with peptide-based therapies is immunogenicity. As a human peptide fragment, pTH (28-48) might be considered less likely to trigger an immune response compared to non-native or significantly modified sequences. However, the risk of developing antibodies that could neutralize the peptide's effects or cross-react with endogenous hormones remains an area warranting detailed investigation.

Owing to its potential interactions with cellular signaling mechanisms, it is also important to evaluate pTH (28-48) for any unintended long-term effects on cellular growth or differentiation, which might contribute to disease processes if not properly controlled.

Clinical trials and preclinical studies that rigorously assess these facets are necessary to establish a comprehensive safety profile for pTH (28-48) (human). In turn, such data will facilitate informed decisions regarding its therapeutic viability and guide appropriate dosing and monitoring protocols to mitigate risks while harnessing its possible benefits for patient care.

How does pTH (28-48) (human) research contribute to the development of future therapies?

Research into pTH (28-48) (human) plays a pivotal role in advancing the development of future therapies by expanding our understanding of parathyroid hormone (PTH) biology and its applications beyond current boundaries. By focusing on a specific mid-region of the hormone, scientific inquiry is redefined, challenging conventional paradigms that have predominantly relied on full-length PTH or its N-terminal fragments.

The investigation into pTH (28-48) provides a unique opportunity to delve into lesser-known pathways and interactions that play significant, yet not fully elucidated, roles in endocrine regulation. This research enriches the foundational knowledge necessary for engineering therapies that are both innovative and effective, especially for conditions that do not respond adequately to existing treatments. By discerning the subtleties of how this peptide modulates calcium and phosphate metabolism, new therapeutic potentials may emerge, specifically targeting inefficiencies or aberrations in these processes.

Moreover, pTH (28-48) research contributes to the design of treatments that are potentially more selective. As the peptide's interactions with different cellular receptors or secondary messengers are characterized, the door opens for developing targeted medications. These could minimize off-target effects and, therefore, reduce complications such as widespread calcium imbalances or the development of kidney stones often seen with more traditional, systemic PTH actions.

One foreseeable impact of this research is the refinement of diagnostic pathways for metabolic bone diseases or calcium-related disorders. By better understanding the role of specific PTH fragments, novel biomarkers might be identified, leading to early and more precise diagnosis. Consequently, this would enable personalized medicine approaches where interventions are tailored not just to symptoms, but underlying physiological profiles.

Additionally, pTH (28-48) research fosters a broader scope of therapeutic collaboration. Potential synergies with other treatments—whether they involve hormonal, pharmaceutical, or even nutraceutical approaches—can be explored for cumulative benefits. As insights gathered from pTH (28-48) research filter into clinical strategies, there's the potential not just to treat but also to fundamentally alter disease progression pathways, particularly in chronic or debilitating conditions.

In conclusion, the pursuit of knowledge surrounding pTH (28-48) (human) is a testament to the ever-evolving landscape of medical science. Its exploration not only informs immediate therapeutic strategies but also sets the stage for revolutionary advancements that harness the body's own regulatory systems, aimed at improving health outcomes and quality of life for patients across the globe.
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