Fact-checked by Grok 2 weeks ago

Apitoxin

Apitoxin, also known as bee venom, is a bitter, colorless toxic liquid produced by the venom glands in the of bees (Apis mellifera) and used primarily as a defense mechanism against predators to protect the colony. It consists of a complex mixture of over 18 biologically active components, including (80-85%), peptides, enzymes, amines, , phospholipids, minerals, carbohydrates, and volatile compounds. The primary bioactive peptide in apitoxin is , which constitutes 40-60% of the dry venom weight and is a 26-amino-acid amphipathic responsible for many of its pharmacological effects through mechanisms such as disruption and pore formation. Other key components include (10-12%), which exhibits enzymatic activity contributing to tissue damage and inflammation; apamin (2-3%), a affecting potassium channels; degranulating (MCD) peptide (2-3%), which triggers release; and , an that enhances spread by breaking down in tissues. Worker bees synthesize and store approximately 300 μg of apitoxin in their sacs, injecting 50-140 μg per , after which the barbed stinger often remains embedded, leading to the bee's death. Apitoxin has been employed in since ancient times, documented in Egyptian, Greek, and Chinese practices for treating conditions such as , , , and dermal diseases. In modern , or bee venom therapy (BVT), it is administered via direct stings, injections, , or topical creams to leverage its anti-inflammatory, analgesic, antimicrobial, and anti-arthritic properties, particularly through inhibition of pro-inflammatory pathways like and reduction of cytokines such as TNF-α and IL-6. Emerging research highlights its potential anticancer effects, where induces and inhibits in various lines by targeting Rac1 and signaling, as well as neuroprotective benefits in models of and by modulating neuroinflammation and T-cell responses; recent 2025 studies also explore nanomaterial-enhanced targeting for and applications in systemic (SLE) and aphthous ulcers. However, its clinical application is limited by risks of allergic reactions, at high doses, potential vascular toxicity such as disruption of vascular and aortic dysfunction observed in 2025 mouse models, and the need for delivery strategies like conjugates to enhance specificity and safety.

Biological Role

Natural Function in Bees

Apitoxin serves as the primary defensive in honey bees, evolved to deter predators and safeguard the from threats such as vertebrates and . In the eusocial Aculeate , including the genus , the system originated from an ancestral reproductive apparatus, initially functioning to paralyze prey, before adapting into a specialized that enhances . This evolutionary shift underscores apitoxin's role beyond predation, incorporating properties that contribute to immunity by inhibiting growth on hive surfaces and nestmates. Apitoxin is produced exclusively in the venom glands of worker bees (Apis mellifera and related species), which are caste members responsible for hive defense. The venom gland consists of a long, filamentous structure located anterior to the sting apparatus in the , lined with secretory cells that synthesize and excrete into a non-muscularized reservoir sac connected to the sting. Upon , worker bees possess an empty venom sac, which gradually fills over the first two weeks of adult life through continuous glandular , reaching peak capacity before the glands begin to later in the phase of their lifespan. This accumulation aligns with behavioral transitions, as older forager workers, often serving as guards, amass the highest reserves to mount collective defenses. A typical worker stores approximately 300 micrograms of dry in its , enabling the delivery of 50–140 micrograms of during stinging events that can recruit additional defenders via alarm pheromones. In colony defense dynamics, this limited individual capacity necessitates coordinated swarming attacks, where multiple stings overwhelm intruders, as a single bee's autotomizing continues pumping post-detachment. Such strategies protect the hive's resources and brood, with 's scaling the response to size. Across species, apitoxin's defensive function remains conserved for colony protection, though potency and antimicrobial efficacy vary; for instance, venom from the giant honey bee () exhibits higher antioxidant activity compared to that of the western honey bee (Apis mellifera) or the smaller , reflecting adaptations to diverse ecological pressures. Africanized honey bees (Apis mellifera scutellata hybrids) deliver lower venom volumes per sting but compensate with aggressive swarming behavior, while overall composition shows minor differences in toxicity across species.

Venom Delivery Mechanism

The stinger, a specialized ovipositor-derived apparatus in female workers, consists of three main components: the piercing part formed by a central stylet flanked by two s, each equipped with approximately 10 rearward-facing barbs for penetration and retention; the sac, which stores 1–2 mg of liquid connected via a narrow (about 39 μm in diameter) to the basal bulb; and associated muscles, including the protractor (M198) and retractor (M199) muscles attached to accessory plates that drive lancet movement. The barbs on the lancets, measuring 12–22 μm in length and arranged in a spiral , facilitate deep insertion up to 1.3 mm while preventing easy withdrawal. The injection process begins with the bee thrusting the stinger forward upon contact, where the stylet and lancets penetrate the target's perpendicularly in about 1.5 seconds, with the lancets reciprocating past the stylet tip to create a pumping . , typically 50–140 μg dry weight (or 0.05–0.14 μL liquid) per sting, is then released through the hollow canal and the gap at the lancet tips into the subcutaneous tissues, with at least 90% delivered within 20 seconds and the process completing in under 1 minute even after . Due to the barbs, the stinger anchors firmly, leading to its detachment from the as it attempts to flee; the autotomized apparatus continues independent pumping for approximately 30 seconds, often resulting in the worker bee's death from loss and organ damage. Upon injection, the venom disperses rapidly into surrounding tissues, eliciting an immediate pain response primarily through the activation of nociceptors by components like melittin, which forms pores in cell membranes and triggers the release of pain mediators such as protons, ATP, and serotonin. This results in localized inflammation, edema, and a sharp stinging sensation that serves as a deterrent. In contrast to other like wasps, which possess smoother or less prominently barbed stingers allowing multiple stings without , honey bees exhibit a one-time aggressive strategy where the barbed retention maximizes delivery at the cost of the worker's life, enhancing protection during threats. This underscores apitoxin's in territorial rather than predation or oviposition.

Chemical Composition

Major Bioactive Peptides

Apitoxin, the of the honeybee Apis mellifera, contains several major bioactive s that constitute a significant portion of its dry weight and contribute to its pharmacological profile. These s, primarily , apamin, and degranulating peptide (MCD), exhibit distinct structural features and biological activities, including membrane perturbation and modulation. Together, they account for over 50% of the 's peptide content, with their interactions enhancing the overall potency of the in disrupting cellular processes. Melittin is the predominant in apitoxin, comprising 40-60% of the dry weight. It consists of 26 in the sequence GIGAVLKVLTTGLPALISWIKRKRQQ-NH₂, forming an amphipathic α-helical structure with a hydrophobic N-terminal region and a hydrophilic, positively charged C-terminal domain. This configuration enables to insert into bilayers, forming pores that lead to membrane disruption and by lysing red blood cells. Apamin represents 2-3% of the dry venom weight and is an 18-amino-acid with the sequence CNCKAPETALCARRCQQH-NH₂, stabilized by two intramolecular bridges (between Cys¹-Cys¹¹ and Cys³-Cys¹⁵). Its compact structure allows selective blockade of small-conductance calcium-activated channels (SK channels), thereby modulating neuronal excitability and function. The structure-function relationship of apamin relies on its positively charged residues, which facilitate binding to regions. Mast cell degranulating (MCD), also known as peptide 401, accounts for 2-3% of the dry weight and features a 22-amino-acid sequence IKCNCKRHVIKPHICRKICGKN-NH₂, cross-linked by two bonds similar to apamin. This cationic induces of s, triggering the release of and other inflammatory mediators through direct interaction with cell surface receptors. Its activity is closely tied to the amphipathic distribution of basic residues, which promotes membrane association and intracellular signaling. The relative proportions of these peptides—melittin dominating at up to 60%, with apamin and MCD each at low single-digit percentages—underlie the synergistic effects in apitoxin's potency, where 's lytic action facilitates the penetration and efficacy of apamin and MCD at target sites. This interplay amplifies venom-induced physiological responses, such as enhanced ion flux and mediator release.

Enzymes and Other Constituents

Apitoxin, the produced by honeybees (Apis mellifera), consists primarily of water in its fresh form, comprising approximately 88% of the total volume, with the remaining dry weight made up of bioactive peptides, enzymes, amines, and other minor compounds. In the dry weight, peptides account for about 50%, enzymes around 12%, and amines approximately 1%, alongside smaller amounts of sugars, , and . These non-peptide components, particularly the enzymes and amines, play key roles in the venom's pharmacological effects, including tissue disruption and immediate physiological responses. The primary enzyme in apitoxin is (PLA2), constituting 10-12% of the dry weight. This enzyme catalyzes the hydrolysis of phospholipids at the sn-2 position, releasing and lysophospholipids, which serve as precursors for inflammatory mediators such as prostaglandins and leukotrienes. The resulting cascade amplifies local and pain at the site of , contributing to the venom's defensive potency. Hyaluronidase, present at 1.5-2% of the dry weight, functions as a that degrades , a key component of the in connective tissues. By breaking down these chains through a hydrolytic mechanism involving acid-base , lowers tissue and facilitates the of other components, enhancing overall penetration and efficacy. This spreading factor activity is characterized by relatively low substrate specificity and optimal activity at neutral , typical of many hyaluronidases. Minor non-peptide constituents include bioactive amines such as histamine (0.5-2%), dopamine (0.1-1%), and norepinephrine (0.1-0.5%) of the dry weight. Histamine induces vasodilation and smooth muscle contraction, triggering immediate allergic-like responses and localized edema. Dopamine and norepinephrine, acting as catecholamines, contribute to nociception by stimulating adrenergic and dopaminergic receptors, thereby intensifying pain signaling and sympathetic activation upon injection. These amines collectively account for the rapid onset of stinging sensation and hypersensitivity reactions observed in envenomation.

Historical Use

Traditional Medicine Practices

Apitoxin, the venom produced by honeybees, has been employed in across various ancient civilizations for its purported therapeutic effects. In , records indicate its use dating back over 5,000 years for treating a range of ailments, though specific applications were often intertwined with broader practices involving bee products. In around 400 BCE, , known as the father of , recommended bee stings to alleviate joint pain and , applying live stings directly to affected areas to induce inflammation believed to counteract chronic conditions. This practice was echoed by Roman figures like , who documented similar uses for pain relief. Traditional Asian practices, particularly in Chinese medicine, incorporated apitoxin since the (206 BCE–220 CE), where it was recorded in medical texts for treating and skin conditions through primitive forms of bee venom . Healers applied it to reduce and promote healing in rheumatic disorders and dermatological issues, viewing it as a means to balance vital energies. In 19th-century European folk remedies, bee stings gained popularity for conditions like and ; for instance, Austrian physician Filip Terč treated over 660 patients with rheumatic arthritis, including gout-related joint pain, using thousands of controlled stings, reporting high success rates in pain relief. Earlier in the century, similar anecdotal uses emerged in rural communities for , with stings applied to pathways to soothe chronic discomfort. Traditional methods of application primarily involved direct stings from live bees to target sites, allowing natural delivery of the venom, though crude extracts were occasionally obtained by squeezing the venom glands or surgical removal from bees. Cultural beliefs across these traditions often attributed "vitalizing" properties to apitoxin, positing that it stimulated blood circulation, enhanced vital energy flow, and restored bodily balance.

Emergence of Apitherapy

, encompassing the therapeutic use of bee products including apitoxin (bee venom), transitioned from ancient folk remedies to a more structured medical approach in the late . This emergence was driven by systematic observations and early clinical documentation in , where physicians began exploring bee stings as a targeted treatment for inflammatory conditions like . Prior empirical uses in ancient civilizations laid the groundwork, but formalized interest arose amid growing scientific inquiry into natural therapies during the industrial era. A pivotal moment came in 1888 when Austrian physician Philipp Terč published "Report on the Peculiar Connection Between Bee Stings and Rheumatism," detailing the first known clinical trial of intentional stings for . Terč's work, based on observations of patients experiencing symptom relief after accidental stings, marked the inception of therapy (BVT) as a deliberate practice and is credited with initiating modern . This publication spurred further experimentation across Europe, where physicians like Franz Kretschy in began advocating for controlled applications of live stings to treat joint disorders. The early 20th century saw gain traction beyond , particularly in the United States, through the efforts of Hungarian-American physician Bodog F. Beck. In 1935, Beck published Bee Venom Therapy, a seminal text compiling clinical cases and advocating BVT for and other ailments, drawing on his clinical experiences with injections. This book popularized the practice internationally and emphasized standardized dosing to mitigate risks. Concurrently, in 1930, the German pharmaceutical company Mack began commercial production of purified bee , enabling safer, non-sting delivery methods and broadening accessibility. Advancements in venom collection further propelled apitherapy's emergence during the mid-20th century. In the 1960s, researchers in developed non-lethal electric shock techniques to harvest from honeybees, improving purity and yield for pharmaceutical use. By the , BVT had gained recognition as a complementary in several , Asian, and countries, reflecting its shift from remedy to a field supported by and technological innovation. Terč's birthday, March 25, was later declared World Day by the international organization Apimondia in 2016.

Therapeutic Applications

Treatment of Inflammatory Conditions

Apitoxin, the venom produced by honeybees, has been employed in therapeutic protocols for managing inflammatory conditions such as (RA) and (OA), primarily through its capacity to alleviate joint swelling and pain. In clinical applications, diluted apitoxin injections administered directly into affected joints or surrounding tissues have demonstrated reductions in inflammation markers and improved mobility in patients with RA and OA. For instance, bee venom acupuncture (BVA), which involves injecting purified apitoxin at points near inflamed areas, has shown efficacy in randomized controlled trials for these arthritic conditions by decreasing joint tenderness and stiffness. Similarly, topical formulations like creams containing apitoxin have been used to target localized inflammation in OA, providing effects without systemic exposure. The anti-inflammatory actions of apitoxin in these conditions are largely attributed to its major components, and (PLA2), which modulate pro-inflammatory pathways. inhibits the production of such as tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6), key mediators in RA and OA progression, by suppressing signaling and reducing inflammatory gene expression in synovial cells. PLA2 further contributes by blocking release, thereby limiting synthesis and amplification in inflamed joints. These mechanisms have been observed in both models of human chondrocytes and animal models of collagen-induced , where apitoxin treatment significantly lowered TNF-α and IL-6 levels compared to controls. Application methods for apitoxin in inflammatory treatments vary to minimize adverse reactions while maximizing , often starting with low doses and titrating based on tolerance. Protocols typically involve BVA with 0.1–1 mg of purified apitoxin per session, administered 1–3 times weekly for 4–8 weeks, using dilutions of 0.005–1.0 mg/mL to affected joints in or patients. Alternative approaches include direct injections of diluted apitoxin (0.1–0.5 mg) or application of sacs from live bees for controlled stinging, particularly for localized issues. Oral supplements containing micro-doses of apitoxin (e.g., 25–50 μg per capsule) are emerging but less studied for , often combined with for joint support. Historical evidence from early 20th-century practices supports these uses, with reports of apitoxin stings effectively treating tendinitis and by reducing swelling in overactive bursa and tendons, as documented in European folk medicine traditions.

Applications in Neurological and Other Disorders

Apitoxin has shown potential in treating neurological disorders such as () by modulating and reducing demyelination in experimental models. However, a 2005 randomized crossover study found no significant improvements in fatigue, motor symptoms, or disease progression in MS patients receiving bee sting therapy. Animal studies using experimental autoimmune encephalomyelitis (EAE), a model for MS, demonstrated that venom reduces clinical symptoms, inflammatory cell infiltration, and pathological changes in the . For (), apitoxin and apamin exhibit neuroprotective properties by preserving dopaminergic neurons and improving motor function in preclinical models. In a model of induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (), bee venom administration provided sustained protection against neurodegeneration, reducing neuronal loss and improving some behavioral outcomes such as locomotor activity, though not rotarod performance. Apamin specifically enhances these benefits by modulating ion channels to mitigate and inflammation in the . These findings indicate apitoxin's role in slowing the chronic degenerative processes characteristic of . Beyond neurological applications, apitoxin's anticancer potential stems primarily from melittin, which induces apoptosis in tumor cells through membrane permeabilization and disruption of cancer cell integrity. In breast cancer cell lines such as MCF7 and MDA-MB-231, melittin suppresses growth factor receptor activation and promotes apoptotic cell death, reducing cell viability and migration. Similarly, in prostate cancer models, melittin triggers apoptosis by altering mitochondrial function and inhibiting proliferation without significant toxicity to normal cells. These mechanisms highlight melittin's selective cytotoxicity against various solid tumors. Apitoxin also demonstrates antimicrobial activity, particularly against bacteria like , via melittin's disruption of bacterial membranes. Studies on methicillin-sensitive and resistant S. aureus strains showed that apitoxin and inhibit bacterial growth, with minimum inhibitory concentrations indicating efficacy comparable to some antibiotics. For skin conditions, apitoxin alleviates symptoms of and through its anti-inflammatory peptides, which reduce lesion severity and T-cell proliferation in affected tissues. Clinical evaluations confirmed that intradermal bee venom injections improve psoriasis plaques more effectively than alone. To enhance targeted delivery and minimize systemic side effects, nanoparticle-encapsulated forms of apitoxin have been developed for these applications. nanoparticles loaded with bee venom or improve and sustain release, showing enhanced antitumor effects in models and in . Similarly, apitoxin-encapsulated nanoparticles exhibit potent antimicrobial activity against pathogens while enabling precise application in skin therapies and . These formulations represent a promising advancement for clinical .

Scientific Research

Pharmacological Mechanisms

Apitoxin, the venom of the honeybee Apis mellifera, exerts its pharmacological effects primarily through its bioactive peptides and enzymes, with being the most abundant and potent component, comprising up to 50% of the dry venom weight. , a 26-amino-acid amphipathic , interacts with membranes by adopting an α-helical conformation that inserts into the , forming transient pores that disrupt membrane integrity and lead to in target cells such as , tumor cells, and inflammatory leukocytes. This pore-forming action facilitates the leakage of cellular contents, including ions and metabolites, and at higher concentrations, it induces or via secondary signaling cascades. Additionally, activates (), an present in apitoxin, which hydrolyzes phospholipids to release , thereby triggering pathways such as the production of resolvins and protectins that mitigate excessive immune responses. Apamin, another key peptide in apitoxin accounting for 2-3% of its composition, functions as a selective blocker of small-conductance calcium-activated (SK) channels, particularly SK2 and SK3 subtypes, which are widely expressed in neuronal and tissues. By binding to the extracellular pore region of these channels, apamin inhibits efflux, thereby prolonging action potentials and increasing neuronal excitability, which can enhance synaptic transmission and modulate learning-related processes in the . In cells, apamin's blockade of SK channels disrupts the hyperpolarization necessary for relaxation, leading to increased contractility in response to stimuli, as observed in vascular and gastrointestinal tissues where SK channels contribute to nitric oxide-mediated . This mechanism underlies apamin's role in altering cellular excitability without directly affecting voltage-gated channels. The pharmacological actions of apitoxin's components are amplified by synergistic interactions, notably through , an constituting about 2% of the , which degrades in the extracellular matrix to enhance the diffusion and bioavailability of peptides like and apamin into target tissues. Collectively, these elements contribute to by regulating profiles; for instance, low concentrations of apitoxin suppress pro-inflammatory cytokines such as TNF-α and IL-6 while promoting mediators like IL-10, thereby balancing immune responses in preclinical models of inflammation. This modulation occurs via inhibition of signaling and activation of regulatory T cells, providing a mechanistic basis for apitoxin's broader potential. Apitoxin's effects exhibit dose-dependent biphasic responses, where low doses (e.g., 0.1-1 μg/mL) predominantly elicit and immunomodulatory outcomes through selective activation of protective pathways, whereas higher doses (e.g., >10 μg/mL) shift toward due to widespread membrane disruption and PLA2-mediated . This duality is evident in cellular assays, where sublytic concentrations of promote resolution of inflammation without cell death, contrasting with lytic doses that cause and tissue damage. Such highlight the importance of precise dosing in therapeutic contexts to harness beneficial mechanisms while minimizing toxicity.

Clinical Studies and Evidence

Clinical studies on apitoxin, the of honeybees, have primarily focused on its potential in managing and associated with , with several randomized controlled trials (RCTs) conducted in during the early 2000s and 2010s. A double-blind RCT involving 80 patients with compared apitoxin to normal saline injections, demonstrating significant reductions in tender and swollen joint counts, morning stiffness duration, , and levels after two months of treatment (p < 0.05). Another RCT with 60 participants with knee reported substantial relief in 82.5% of the apitoxin group compared to 55% in the standard group (p < 0.01), based on patient-reported outcomes. A 2008 prospective RCT in examined apitoxin pharmacopuncture versus warm needling in 49 patients with knee , finding improved scores and function in the apitoxin group, though with small sample sizes limiting generalizability. For neurological disorders, evidence remains mixed, with limited high-quality human trials. A 2005 randomized crossover trial in 26 patients with relapsing-remitting tested live bee stings (delivering apitoxin) versus , showing no significant reduction in disease activity, , or after 24 weeks, alongside increased risk of allergic reactions. In contrast, a non-randomized in 10 Iranian patients with reported decreased functional and improved following subcutaneous apitoxin injections over six months, though without a control group and small cohort size. For Parkinson's disease, three RCTs indicated symptom improvement via Unified Parkinson's Disease Rating scores in two studies (p < 0.05), but no benefit in the third, highlighting inconsistent outcomes. Anticancer research on apitoxin has advanced through and animal models in the , showing promise but lacking robust human data. Studies demonstrated that apitoxin and its component induce and inhibit in , , , and other cancer cell lines, with targeted formulations enhancing specificity and reducing toxicity in murine models. For instance, honeybee venom suppressed growth factor receptor activation in cells , suggesting potential as an adjunct therapy. As of 2025, recent preclinical studies have further demonstrated its effects on cells and the use of melittin-based nanoparticles for enhanced cancer therapy. However, no phase I human trials for were identified as of 2025, with preclinical work emphasizing the need for safer delivery systems to translate findings clinically. Meta-analyses up to 2025 underscore efficacy gaps in apitoxin across conditions. A 2020 systematic review of 12 RCTs (n=904) for various conditions, including musculoskeletal such as , found significant reduction (e.g., visual analog scale improvements, p < 0.05) but noted small sample sizes (often <50 per arm), short durations (4–12 weeks), and high risk of due to inadequate blinding. For neurological applications, the review highlighted variable results and called for larger, standardized trials to heterogeneity in dosing and administration. Anticancer meta-analyses were absent, with reviews stressing the transition from promising preclinical anti-proliferative effects to studies, hampered by issues and concerns. Overall, while apitoxin shows potential for symptom alleviation, limitations like limited and underreporting necessitate further rigorous RCTs.

Safety and Regulation

Potential Adverse Effects

Apitoxin, the produced by honeybees, commonly induces local reactions at the of exposure, manifesting as pain, swelling, and . These effects are primarily attributed to the release of , which promotes and fluid leakage leading to swelling and redness, and , a major component that disrupts cell membranes and triggers intense pain through activation. In clinical settings, such as bee venom therapy, these local symptoms occur frequently, with studies reporting pruritus, , and in up to 35.8% of cases across audits and studies. Systemic effects represent a more serious concern, particularly , which affects approximately 1-3% of the population sensitized to hymenopteran s and arises from IgE-mediated . Symptoms include , , urticaria, and potentially life-threatening airway obstruction, with incidence rates in immunotherapy cohorts reaching up to 14% for broader systemic reactions, though severe is rarer at around 0.014-0.2%. These reactions can occur even with diluted apitoxin in therapeutic applications, underscoring the need for careful monitoring. Rare complications from apitoxin exposure include , characterized by muscle breakdown and potential , typically following multiple stings that overwhelm the body's detoxification capacity. This condition has been documented in cases involving massive , leading to elevated levels and renal failure in up to 25% of severe instances. , an immune complex-mediated reaction, may also develop after repeated therapeutic exposures, presenting with fever, , rash, and approximately 7-14 days post-injection. Severity of adverse effects is influenced by the dose of apitoxin delivered and individual factors such as prior or underlying conditions. For instance, more than 50 stings can precipitate systemic beyond allergic responses, while fatalities from overload generally require 500-1,000 stings in non-allergic individuals, though allergic persons face heightened risk from far fewer. Heightened , often assessed via testing, amplifies the potential for severe outcomes in both natural encounters and controlled .

Contraindications and Guidelines

Apitoxin therapy is absolutely contraindicated in individuals with a history of to bee venom, as it poses a severe of life-threatening allergic reactions. It is also contraindicated during and due to potential adverse effects on fetal development and , as well as in patients with cardiovascular instability, such as uncontrolled or recent , where the venom's hypotensive or inflammatory effects could exacerbate conditions. Prior to initiating therapy, testing is recommended, typically involving an of 0.05 mL of diluted bee venom to assess . In terms of regulatory status, the U.S. Food and Drug Administration (FDA) classifies purified as a biological product and has approved its use solely for in desensitizing individuals allergic to insect stings, but it remains unapproved for most therapeutic applications like treating inflammatory or neurological conditions as of 2025. In contrast, in , bee venom formulations have been approved for treating since 2003. is considered part of traditional and complementary medicine in various cultures. The (WHO) encourages the integration of evidence-based traditional and complementary medicines into national health systems under proper supervision to ensure safety. Safe administration protocols emphasize starting with micro-doses to minimize risks, such as 0.01 mg (10 μg) of purified apitoxin via subcutaneous injection, gradually escalating based on tolerance under medical supervision. Monitoring during sessions includes assessment every 15-30 minutes and availability of emergency equipment like epinephrine auto-injectors for management, with sessions limited to 12-20 for chronic conditions and post-treatment observation for at least 30 minutes. Ethical and legal considerations for apitoxin use in clinics require obtaining from patients, detailing potential risks, lack of FDA approval for non-desensitization uses, and the experimental nature of the therapy, while ensuring administration only by qualified practitioners to comply with local medical regulations.