Synonym |
Calcitonin (porcine) |
Species |
Porcine |
Protein Accession |
P01258 |
Purity |
Greater than 95% |
Endotoxin Level |
Less than 1 EU/μg |
Biological Activity |
Not specified |
Expression System |
Not specified |
Fusion Tag |
None |
Predicted Molecular Mass |
About 3354 Da |
Formulation |
Lyophilized from a sterile-filtered solution in 0.1% TFA |
Reconstitution |
Reconstitute in water to a concentration of 0.1-1 mg/ml |
Storage & Stability |
Store lyophilized protein at -20°C. Aliquot reconstituted protein and store at -20°C. Avoid
repeated freeze-thaw cycles. |
FAQ
What is Calcitonin (porcine), and how does it function in the body?
Calcitonin is a hormone that
plays a crucial role in calcium and bone metabolism. It is naturally produced in the parafollicular
cells (also known as C-cells) of the thyroid gland in humans and other animals. Calcitonin (porcine)
specifically refers to the calcitonin hormone that is derived from pigs. This hormone is of particular
interest because its structure and function are similar to that of human calcitonin, making it a useful
model for studying the physiological actions and therapeutic potential of calcitonin analogs in
humans.
In its physiological role, calcitonin lowers blood calcium levels when they rise above a
certain threshold. It achieves this by inhibiting the activity of osteoclasts, which are the cells
responsible for breaking down bone tissue and releasing calcium into the bloodstream. By reducing
osteoclast activity, calcitonin effectively slows the release of calcium from bones, contributing to
bone preservation and maintaining proper calcium homeostasis in the body. Calcitonin also reduces renal
tubular reabsorption of calcium, thereby increasing calcium excretion in the urine, which further aids
in reducing blood calcium levels.
Beyond its critical role in calcium homeostasis, calcitonin has
been studied for its potential therapeutic applications. Conditions like osteoporosis, Paget's disease,
and hypercalcemia of malignancy are associated with excessive bone resorption or elevated calcium
levels, making calcitonin a candidate for treatment. In osteoporosis, for instance, the goal of
calcitonin therapy is to inhibit further bone loss and reduce the risk of fractures by lowering bone
turnover rates.
While calcitonin derived from porcine sources is particularly studied due to its
comparability to human calcitonin, it's important to note the differences as well. The slight molecular
variations mean that while porcine calcitonin can be informative in research and preclinical studies,
synthetic or recombinant human calcitonin is usually preferred for clinical treatments in humans to
avoid immune reactions and compatibility issues. Understanding these nuances is essential in both
research and therapeutic contexts.
How is Calcitonin (porcine) used in research, and what are its
potential benefits?
Calcitonin (porcine) holds significant value in scientific research,
predominantly due to its structural and functional similarity to human calcitonin, which allows it to
serve as a model for understanding the hormone's role in various physiological and pathological
processes. One of the principal areas of research involving calcitonin (porcine) is its influence on
bone metabolism and calcium homeostasis. Researchers utilize calcitonin to study its effects on
osteoclasts, the bone-resorbing cells, to gain insights into how bone density can be preserved and how
conditions like osteoporosis can be managed or prevented.
In addition to bone health, calcitonin
(porcine) provides a framework for exploring its analgesic properties, which have been of growing
interest in pain management research. Studies have suggested that calcitonin may have a direct effect on
certain types of nociceptive pathways, which are related to the sensory neurons that respond to
potentially damaging stimuli by sending pain signals to the brain and spinal cord. Research utilizing
porcine calcitonin can thus help clarify its potential mechanisms of action in modulating pain, opening
avenues for new therapeutic strategies for chronic pain conditions.
Calcitonin (porcine) is also
employed to probe the regulatory mechanisms of calcium and phosphate metabolism, particularly in the
context of endocrine functions and disorders. By understanding how calcitonin affects other hormones
involved in mineral metabolism, such as parathyroid hormone and vitamin D, researchers can better
comprehend the complex interactions that maintain mineral balance and apply this knowledge to diseases
where these processes are dysregulated.
Moreover, calcitonin (porcine) serves as a critical tool
in pharmacological research to assess the efficacy and safety of calcitonin analogs or derivatives being
developed for therapeutic use. By experimenting with calcitonin sourced from porcine models, researchers
can simulate human-like responses in preliminary studies, which helps in optimizing dosages, delivery
methods, and minimizing potential side effects in subsequent human trials.
Ultimately, the
benefits derived from research using calcitonin (porcine) are manifold. From improving our understanding
of fundamental biological processes to aiding the development of novel treatments for diseases affecting
millions worldwide, calcitonin (porcine) stands as an invaluable resource in both basic and applied
biomedical research.
Are there any known side effects associated with the use of Calcitonin
(porcine)?
Calcitonin (porcine), like many biologically active peptides used in research and
clinical settings, can be associated with a range of side effects, although these can vary depending on
the method of administration and the species being studied. It's crucial to distinguish between side
effects observed in laboratory research settings and those encountered in clinical scenarios with
synthetic or recombinant human calcitonin, as direct human use of porcine calcitonin is less common due
to the potential for immunogenic reaction.
In research environments where calcitonin (porcine) is
used for animal studies, side effects are often evaluated to understand not only the basic
pharmacodynamics of the hormone but also to anticipate possible reactions in human analogs. Commonly
observed effects in animal studies, particularly in mammals, include variations in blood calcium levels
due to its potent activity on inhibiting osteoclastic bone resorption. Given calcitonin’s ability to
rapidly decrease serum calcium, hypocalcemia can occur if dosages are not carefully managed. Symptoms of
hypocalcemia include muscle spasms, tingling, and carpopedal spasms, which are important parameters to
monitor in research settings.
Another consideration is the impact of calcitonin (porcine) on the
gastrointestinal system. Nausea and vomiting are frequently reported side effects when calcitonin is
administered in ways that allow systemic absorption, such as via injection. These reactions are believed
to be linked to calcitonin’s interactions with central nervous system pathways that control nausea but
also reflect its broad systemic hormone effects.
Moreover, there is the potential for allergic
reactions or immune response when a non-human peptide hormone like porcine calcitonin is introduced into
a different species. These immune reactions can range from mild, such as localized skin reactions or
irritation, to more severe anaphylactic reactions, although it’s worth noting that such adverse effects
are less common with calcitonin derived from recombinant sources specifically engineered for human
compatibility.
In sum, while calcitonin (porcine) is a vital tool for understanding bone
metabolism and developing therapeutic interventions, understanding and managing its side effects is
crucial, particularly where translational research aims to apply these findings to human medicine. The
continued study of its safety profile helps inform the development of safer, more effective therapeutic
alternatives in treating disorders like osteoporosis and related conditions.
What are the
differences between Calcitonin (porcine) and synthetic or recombinant human calcitonin used in medical
treatments?
Calcitonin (porcine) and synthetic or recombinant human calcitonin, while similar in
function, exhibit distinct differences that make each suitable for different applications—calcitonin
(porcine) predominantly in research, and synthetic human calcitonin typically in therapeutic contexts.
The primary difference lies in their origin and molecular structure. Calcitonin (porcine) is a natural
hormone extracted from pigs, structured to mimic the calcitonin as found in porcine systems. In
contrast, synthetic or recombinant human calcitonin is engineered to match the exact amino acid sequence
of human calcitonin or to be very closely related. This close mimicry is crucial for reducing immune
responses during therapeutic use in humans.
One significant advantage of using recombinant human
calcitonin is its reduced immunogenicity compared to porcine calcitonin. While porcine calcitonin can
evoke an immune response if used directly in humans due to minor molecular differences perceived as
foreign by the immune system, synthetic or recombinant human calcitonin minimizes the risk of such
adverse immune reactions. The recombinant form is preferred in clinical settings for treatments like
osteoporosis, where long-term hormone therapy may be required, and where patient tolerance and immune
response are critical considerations.
Another critical difference is related to their
pharmacokinetic properties. Synthetic or recombinant calcitonin is designed to optimize its stability,
absorption, and activity when administered, whether by injection, nasal spray, or oral formulations,
whereas porcine calcitonin’s use is mainly confined to investigational settings where such parameters
are less critical to manage. The delivery methods for human calcitonin are also continuously being
improved to enhance patient adherence and minimize potential side effects such as gastrointestinal
discomfort.
In terms of research applications, calcitonin (porcine) remains a valuable tool for
preliminary studies, preclinical trials, and educational purposes. Its utility in foundational studies
helps establish baseline responses and understand hormone action mechanisms. However, due to its
potential for cross-species immune interactions, researchers ultimately prefer derivatives that can be
safely transitioned to synthetic or recombinant human formulations for therapeutic
exploration.
Ultimately, both forms of calcitonin have their roles, but the evolution of
synthetic recombinant human calcitonin offers health care providers more reliable and applicable options
for effective patient care. This distinction underscores the importance of precision and orientation
toward patient safety and efficacy in therapeutic drug design and deployment.
What are the
current research trends involving Calcitonin (porcine)?
Recent research trends involving
Calcitonin (porcine) have reflected an increased understanding of its multifaceted role, beyond
traditional approaches focusing solely on calcium and bone metabolism. Scientists are exploring broader
implications, such as its potential neuroprotective effects, applications in cancer treatment, and the
exploration of its role in pain management.
A prominent area of study is the investigation of
calcitonin’s potential neuroprotective properties. Emerging evidence suggests that calcitonin may help
in neural health and cognitive function, offering protective benefits against neurodegenerative diseases
such as Alzheimer’s disease. Research is being conducted to understand the pathways through which
calcitonin influences neural cells, potentially reducing oxidative stress and combating neuronal
apoptosis. Calcitonin (porcine) serves as a model peptide in exploring these effects before
transitioning into studies that can lead to human therapies.
Another significant trend is
examining calcitonin’s implications in oncology, particularly in managing hypercalcemia related to
malignancies. Its role in modulating calcium levels is well-documented, but ongoing research seeks to
understand how calcitonin could be integrated into more comprehensive cancer treatment protocols.
Studies are examining its potential to affect tumor growth and metastasis, although these areas are
still at an early stage, warranting further in-depth exploration to draw definitive
conclusions.
Pain management also remains a critical research focus, as calcitonin has been
observed to have analgesic properties in clinical and preclinical studies. Researchers are dedicating
efforts to delineating the pathways and mechanisms through which calcitonin exerts these effects, which
involve modulating sensory inputs and inflammatory responses possibly via central nervous system
pathways. Calcitonin (porcine) models are instrumental in these early-stage investigations as scientists
seek to validate findings that can improve chronic pain conditions' management.
In addition to
these applications, researchers continue to explore the hormone’s mechanisms in greater detail,
employing calcitonin (porcine) in experimental setups to explore receptor interactions, signaling
pathways, and genetic influences on its activity. Such foundational research is crucial for designing
next-generation analogs with improved efficacy and reduced side effects.
These research endeavors
reflected an overarching goal of harnessing calcitonin’s physiological and pharmacological potential,
indicating a promising future where this hormone might contribute to medical breakthroughs across
diverse domains. Explorations strive not only to deepen theoretical understanding but also to translate
these insights into tangible health solutions.