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.