Toxins have evolved in plants, animals and microbes, often as part of defensive and/or prey-capture strategies. Although non-peptide toxins are typically orally active, peptide toxins are usually found in animal venoms associated with specialized envenomation apparatus that allows their delivery into the soft tissue of animals via subcutaneous, intramuscular or intravenous routes.
Crude venoms contain a diverse array of different peptides, many of which are bioactive. Small peptides present in the venom of cone snails, a family of widely distributed marine molluscs, are highly structured mini-proteins that have evolved in ∼ 500 species of fish-, mollusc- and worm-hunting cone snails for rapid prey immobilization and defence. Their small size, relative ease of synthesis, structural stability and target specificity make them important pharmacological probes.
Venom peptides target a wide variety of membrane-bound protein channels and receptors. Of the cone snail venom peptides characterized to date, a surprising number have been found to be highly selective for a diverse range of mammalian ion channels and receptors associated with pain signalling pathways, including the nicotinic acetylcholine receptors (α-conotoxins), the noradrenaline transporter (χ-conopeptides), sodium channels (μ- and μO-conotoxins), calcium channels (ω-conotoxins), the N-methyl-D-aspartate receptor (conantokins) and the neurotensin receptor (contulakins).
It is well established that Ca2+ influx into nerve terminals through voltage-sensitive calcium channels (VSCCs) is the trigger that initiates neurotransmitter release. ω-Conotoxins are unique tools with which to identify and determine the physiological role of different neuronal VSCCs and might be potent analgesics for chronic pain.
Like the structurally related VSCCs, voltage-sensitive sodium channels (VSSCs) play a key role in the nervous system. A number of these VSSC subtypes are implicated in clinical states such as pain, stroke and epilepsy. Venoms have evolved to target these channels. Although sodium channel activators are typically toxic, subtypes-elective inhibitors may have considerable therapeutic potential.
Potassium channels are a large and diverse family of proteins implicated in the regulation of many cellular functions. Of the numerous potassium channel-blocking peptides that have been identified, only a small number have shown promising results in animals.
Chloride channels are also among the many membrane proteins overexpressed in different types of cancers. Chlorotoxin isolated from the scorpion Leiurus quinquestriatus binds to specific Ca2+-activated chloride channels and certain tumours and gliomas, and so might have potential in the treatment of cancer.
The first example of a successful venom-based drug is Captopril, which inhibits the angiotensin-converting enzyme, an essential enzyme for the production of angiotensin, a vasoconstrictor associated with hypertension.
As a consequence of their high selectivity, venom peptides have proved particularly useful for in vitro and in vivo proof-of-concept studies. However, for therapeutic applications, a number of issues associated with safety, pharmacokinetics and delivery need to be addressed. It remains to be determined how many of the peptides that are present in venoms can find a clinical utility.
Venomous animals have evolved a vast array of peptide toxins for prey capture and defence. These peptides are directed against a wide variety of pharmacological targets, making them an invaluable source of ligands for studying the properties of these targets in different experimental paradigms. A number of these peptides have been used in vivo for proof-of-concept studies, with several having undergone preclinical or clinical development for the treatment of pain, diabetes, multiple sclerosis and cardiovascular diseases. Here we survey the pharmacology of venom peptides and assess their therapeutic prospects.
Toxins have evolved in plants, animals and microbes multiple times as part of defensive and/or prey capture strategies. Non-peptide toxins are typically orally active and include many food-borne toxins of DINOFLAGELLATE origin, such as the ciguatoxins and brevetoxins which activate voltage-sensitive sodium channels1, the diarrhoetic shellfish poisons which inhibit protein phosphatases2,3, and the paralytic shellfish poisons (saxitoxins) which inhibit sodium channels. Puffer fish and crabs apparently accumulate lethal levels of another sodium-channel inhibitor (tetrodotoxin) from bacteria4, whereas certain frogs can accumulate alkaloids, such as batrachotoxin and epibatidine, through their diet5. Many of these toxins have proven to be invaluable research tools and have provided leads for potential new therapies. An example is provided by epibatidine and its analogues, which produce potent antinociception6,7, probably by activating certain nicotinic acetylcholine receptors that stimulate the release of noradrenaline in the spinal cord8.
By contrast, peptide toxins are usually found in animal venom associated with specialized ENVENOMATION APPARATUS that allows their delivery into the soft tissue of animals via subcutaneous, intramuscular or intravenous routes (Fig. 1). Most venoms comprise a highly complex mixture of peptides, often with diverse and selective pharmacologies. Despite this diversity, venom peptides seem to have evolved from a relatively small number of structural frameworks that are particularly well suited to addressing the crucial issues of potency and stability (Fig. 2). It is this evolved biodiversity that makes venom peptides a unique source of leads and structural templates from which new therapeutic agents might be developed.
In this review, peptides found in the venom of cone snails, spiders, scorpions, snakes, the Gila monster lizard and sea anemone (Fig. 1) are discussed in relation to their therapeutic potential, and that of the targets they modulate. Where possible, we focus on venom peptides that have been investigated for in vivo efficacy. The reader is directed to other publications that discuss related venom peptides that have been investigated in vitro in terms of their potency, selectivity and mechanism of action.
Unravelling venom biodiversity
As indicated above, crude venoms contain a diverse array of different peptides, many of which are bioactive. Nowhere is this diversity more apparent than within the small peptides (conotoxins and conopeptides) present in the venom of cone snails, a family of widely distributed marine molluscs (Fig. 3). These peptides are highly structured mini-proteins that have evolved in ∼500 species of fish-, mollusc- and worm-hunting cone snails for rapid prey immobilization and defence (see Fig. 3 for examples). Their small size, relative ease of synthesis, structural stability and target specificity make them important pharmacological probes. It is estimated that >50,000 conopeptides exist, but <0.1% have been characterized pharmacologically. Of those characterized to date, a surprising number have been found to be highly selective for a diverse range of mammalian ion channels and receptors associated with pain signalling pathways, including the nicotinic acetylcholine receptors (α-conotoxins), the noradrenaline transporter (χ-conopeptides), sodium channels (μ- and μO-conotoxins), calcium channels (ω-conotoxins), the N-methyl-D-aspartate (NMDA) receptor (conantokins) and the neurotensin receptor (contulakins) (Table 1). Cone snails are not the only species that produce peptides in their venom; however, those found in spiders, snakes, sea anemones and scorpions are typically of larger size.
How are peptides of interest identified amongst the large numbers of related molecules that are present in animal venoms? In general, three approaches are taken. Traditionally, assay-directed fractionation has been used. The development of novel high-throughput assays for a diversity of targets, along with improved separation and sequencing capabilities, have simplified peptide isolation and characterization. For example, ω-conotoxin GVIA (ω-GVIA) was first isolated from Conus geographus venom fractions that caused shaking in mice following intracerebroventricular administration9, whereas ω-CVIA–D were isolated from fractions that inhibited binding of 125I-GVIA to rat brain membranes10. The polymerase chain reaction and chemical approaches (for example, mass spectrometry) are increasingly being used to overcome the bias associated with assay-directed methods, which identify the major activity (potency × quantity) at the expense of less abundant components. Chemical synthesis of the peptide allows confirmation of activity and further characterization across multiple targets, both in vitro and in vivo.
Optimizing venom peptides
Venom peptides need to be sufficiently stable to survive chemical degradation in solution at ambient temperature and enzymatic degradation by processing proteases present in the venom itself11, as well as those in the tissues of prey species. This stability is often achieved naturally through the use of post-translational modifications (PTMs) and/or disulphide bonds which fold the peptide into a stabilized structure. Typical PTMs include amidation (C-terminal), sulphation (Tyr), bromination (Trp), glycosylation (Thr), γ-carboxylation (Glu), hydroxylation (Pro), pyroglutamation, N-C-cyclization and isomerization to D-amino acids. Specific enzymes are used during the production of venom peptides to introduce these modifications at specific locations, which can enhance peptide bioavailability and potency in addition to stability. Despite these modifications, venom peptides are not always optimal for all requirements associated with potential therapeutic applications. Issues surrounding the therapeutic use of peptides include formulation, cost of production, stability, selectivity and mechanism of action. Chemical synthesis of analogues allows structure–activity relationships (SARs) to be developed that can guide the coordinated optimization of these features. As part of this process, optimized oxidation conditions need to be established to favour the correct formation of disulphide bonds after synthesis (see Table 1).
Identified complementary interactions between the peptide and its target can be used to define the docking of the peptide with the goal of guiding the design of analogues (including small molecules) with tailored properties at specific molecular targets (Box 1). This approach is particularly relevant to the larger venom peptides, which are unlikely to escape the surveillance of the immune system. One limitation of peptides is their inability to cross epithelial layers, including the blood–brain barrier. Owing to their relatively large size and hydrophilic nature, the oral bioavailability of venom peptides (∼10–40 amino acids) is generally poor. This typically means that peptides need to be administered to the site of action by either intravenous, intrathecal, intraperitoneal, intramuscular, subcutaneous or epidural injection. Emerging approaches to improving peptide delivery, such as lipophilic modifications12, might eventually allow oral delivery to peripheral and central targets. However, combining targeted delivery with a restricted target distribution can be an advantage when a particular target of interest is found both centrally and peripherally, and efficacy is derived from drug interaction at the central sites, but side effects arise from an action of the drug in the periphery, for example.
The selectivity and mechanism of action of venom peptides also needs to be taken into consideration in anticipation of putative adverse side effects. Most ion-channel modulators that are used in the clinic and that have good therapeutic indices are state-dependent blockers13. These compounds preferentially associate with a gating conformation of the channel that is relevant for drug efficacy; they derive safety from their lower affinity for different conformational states of the channel that are present in other tissues, or which are found only in the absence of disease. So, small molecules can often achieve functional selectivity despite lacking target selectivity. In the case of pore-blocking peptides, the mechanisms of functional selectivity are not obvious, as it is thought that these agents bind with similar affinity to the different gating conformations of the channel. To overcome this limitation, it might be possible to exploit the relatively undeveloped families of gating-modifying peptides. Potassium-channel-gating modifiers, for example, seem to bind to a region of the protein that is only available when the channel opens14,15,16, and could display target selectivity because there is little conservation in the sequence of the putative receptor site for these peptides within related channels17. However, channel-gating modifiers have not been investigated for therapeutic benefit in animal models. One of the limitations in their use could be related to the difficulty of obtaining large amounts of these peptides. Improvements in their synthesis and folding will facilitate the evaluation of these agents18.
Pharmacology of venom peptides
Venom peptides target a wide variety of membrane-bound protein channels and receptors. Examples of the structural diversity of membrane protein targets with therapeutic potential are shown in Fig. 4 (see Box 1 for further details). Venom peptides acting at these and other targets are described below.
Calcium channel peptides. It has long been established that Ca2+ influx into nerve terminals through voltage-sensitive calcium channels (VSCCs) is the trigger that initiates neurotransmitter release. In recent years, much has been learned about the nature of VSCCs. These channels have been classified into six groups according to their electrophysiological and pharmacological properties, and are termed L-, N-, P-, Q-, T- and R-type channels19,20,21. Studies investigating the role of VSCCs in neurotransmitter release have indicated that the release of a particular neurotransmitter is coupled to the activity of different calcium channel subtypes in different neurons. In addition, multiple splice variants of calcium channels exist in central and peripheral tissues22. Given this diversity, considerable opportunity exists to develop selective inhibitors of VSCCs.
The ω-conotoxins are unique tools with which to identify and determine the physiological role of different neuronal VSCCs. A range of different VSCC peptides are produced by cone snails9,10,23, spiders24,25,26,27 and snakes28. As N-type (Cav2.2) VSCCs participate in the ascending pain pathways (see Fig. 5), and are upregulated in the spinal cord in chronic pain states29 along with the auxiliary α2δ1 subunit30, it is not surprising that ω-conotoxins specific for N-type VSCCs are potent analgesics31,32. Extensive SAR studies have allowed the development of a pharmacophore model for ω-conotoxins33 that might allow the rational development of specific N-type VSCC inhibitors. Recently, ω-CVID was found to inhibit an otherwise resistant VSCC found in parasympathetic nerve terminals, despite being ∼106-fold selective for N-type over P/Q-type VSCCs34. The implications of inhibiting this 'R-type' calcium channel for pain conditions are unclear, but these neurons arise from cell bodies in the spinal cord that could be involved in spinal signal processing. Sub-nanomolar bolus intrathecal doses of ω-MVIIA or ω-CVID produce analgesia for up to 24 hours in inflammatory35 and neuropathic36 pain models (see Fig. 5), with ω-CVID displaying a wider therapeutic index than ω-MVIIA. ω-MVIIA (SNX111/Ziconotide/Prialt; Elan) is in late Phase III trials, and ω-CVID (AM336; AMRAD) is entering Phase II trials for the treatment of chronic pain. Inhibitors able to target specific VSCC splice variant/auxilliary subunit combinations specifically associated with ascending pain pathways could produce analgesia with fewer side effects.
Sodium-channel toxins. Like the structurally related VSCCs, voltage-sensitive sodium channels (VSSCs) are crucial to the functioning of the nervous system. On the basis of their susceptibility to blockade by tetrodotoxin (TTX), which acts at 'site 1' in the P-loop region of the α-subunit, VSSCs can be divided into TTX-sensitive (TTX-S) and TTX-resistant (TTX-R) classes; members of both classes share considerable sequence similarity and are closely related structurally37. The former class includes the neuronal TTX-S type I/Nav1.1 channel, the type II/Nav1.2 channel, the type III/Nav1.3, PN1/Nav1.7 and PN4/Nav1.6 channels, and the skeletal muscle TTX-S μ1/Nav1.4 channel. The TTX-R sodium channels include the cardiac H1/Nav1.5 channel, which is partially TTX-resistant, and the neuronal TTX-R SNS/ PN3/Nav1.8 and NaN/PN5/Nav1.9 channels (Ref. 37). A number of these VSSC subtypes are implicated in clinical states such as pain (see Fig. 5), stroke and epilepsy. For example, there is now compelling evidence that PN3/SNS/Nav1.8, a TTX-R sodium channel located specifically in sensory neurons38,39, is important in neuropathic pain40,41. Given their crucial role in the central and peripheral nervous system, it is not surprising that a number of venoms from spiders42,43, sea anemone and coral44,45,46, scorpions47, and cone snails48,49,50 have evolved to target these channels. In addition, an unusual spider toxin has been identified that inhibits proton-gated sodium channels associated with pain pathways51.
Although sodium-channel activators are typically toxic, subtype-selective inhibitors might have considerable therapeutic potential. Despite this therapeutic potential, little progress has been made towards the development of peptides that are subtype-selective inhibitors of VSSCs. Given the latent pharmacology revealed by TTX, pore blockers such as the μ-conotoxins52 seem to hold most potential as subtype-selective inhibitors of VSSCs. By contrast, the intra-membrane local anaesthetic site, where many classes of small molecules act, is conserved across the different VSSCs and could be more problematic for conferring subtype discrimination. However, state- and frequency-dependent blockade for many drugs that bind in this region, such as phenytoin, carbamazepine, lamotrigine and lidocaine, has allowed the therapeutic use of these compounds in the treatment of epilepsy, neuropathic pain and arrhythmias.
Potassium-channel toxins. Potassium channels are a large and diverse family of proteins that are implicated in the regulation of many cellular functions, such as smooth muscle and neuronal excitability, proliferation, electrolyte secretion and volume regulation. Peptide inhibitors have helped elucidate the physiological role of some potassium channels in native tissues, including Kv1 channels in the enteric nervous system53, and high-conductance calcium-activated potassium channels in smooth muscle tissues such as bladder54. Obviously, blocking potassium channels will lead to many pathophysiological conditions. There are, however, examples in which the blockade of a specific potassium channel can produce a desired therapeutic outcome. For instance, first-line therapy for the treatment of type 2 diabetes are sulphonylureas, a group of compounds that block the ATP-dependent potassium channel in pancreatic β-cells55. In addition, dofetilide (Tikosyn; Pfizer), an inhibitor of the cardiac rapid delayed rectifier channel IKr, has been approved by the US FDA for the conversion and maintenance of sinus rhythm in patients with atrial fibrillation56. Cognitive enhancers, such as linopirdine and XE-991, are blockers of cloned KCNQ channels that underlie the native muscarinic current in a variety of neurons57. These agents have been shown to enhance the stimulus-evoked release of neurotransmitters, including acetylcholine, in the central nervous system, and to improve learning and memory in behavioural animal models. In a number of clinical trials with chronic spinal cord injury and multiple sclerosis patients, the nonselective potassium-channel blocker 4-aminopyridine has been shown to produce improvements in sensory and motor function56. It is thought that in demyelinated axons, the expression and distribution of channels such as Kv1.1 and Kv1.2 is altered, leading to increased channel activity and, as a consequence, to axonal dysfunction. The erythrocyte calcium-activated potassium channel is the pathway responsible for potassium efflux from the cell that drives chloride and water loss. As such, blockers of the erythrocyte channel have utility in the treatment of sickle-cell anaemia by preventing erythrocyte dehydration58. Blockers of the voltage-gated potassium channel Kv1.3 have been shown to inhibit the delayed-type hypersensitivity reaction to tuberculin in YUCATAN MINI-PIGS, indicating that these channels could be targets of immunosuppressants59,60. Together, these findings indicate that the inhibition of potassium channels can have important therapeutic consequences. Peptide blockers of potassium channels that bind to external epitopes represent an interesting alternative for drug intervention61. These peptides have been shown to display good selectivity and potency for certain potassium channels and, because of their lack of cell penetration, should not cause the side effects that result from binding to intracellular targets.
Of the numerous potassium-channel-blocking peptides that have been identified, only a small number have shown promising results in animals. The first peptide to be tested in vivo was margatoxin (MgTX) from the scorpion Centruroides margaritatus, which is a potent blocker of the voltage-gated potassium channels Kv1.1, Kv1.2, and Kv1.3 (Ref. 70). In human T cells, Kv1.3 channels control the resting membrane potential, and their blockade causes membrane depolarization62 and, as a consequence, an attenuation of the increase in cytoplasmic calcium levels that occur on T-cell activation59. In in vitro assays, Kv1.3 blockers inhibit human T-cell proliferation, indicating that Kv1.3 channels represent a target for the development of novel immunosuppressants59,63,64. MgTX depolarizes the T cells of both pigs and humans in vitro59, with a plasma t1/2 of ∼2 hours in pigs. MgTX also inhibits the delayed-type hypersensitivity reaction to tuberculin in the mini-pigs, as determined by both the size of induration and the extent of T-cell infiltration59. The effect of MgTX was similar in magnitude to that of the immunosuppressant agent FK506, although lower concentrations of peptide were needed to achieve similar efficacy. No major toxicity events were noticed in these experiments, with hypersalivation and diarrhoea53 observed during continuous infusion of the peptide. However, bolus intravenous injection of higher doses of MgTX led to plasma concentrations >10 nM that caused transient hyperactivity in the pigs, indicating a possible effect on Kv1.1 and Kv1.2 channels in the brain. A possible central effect has particular relevance to immunosuppressed patients who might have a compromised blood–brain barrier.
ShK from the sea anemone Stichodactyla helianthus also blocks Kv1.1 and Kv1.3 channels and has shown efficacy in animal models of multiple sclerosis. ShK has a different three-dimensional structure to MgTX and related scorpion toxins (see Fig. 2)65, but blocks potassium channels by binding to the outer vestibule and plugging the pore, in a similar manner to MgTX. Multiple sclerosis is a disease of the central nervous system of immunological aetiology, and is characterized by disseminated patches of demyelination in the brain and spinal cord, which results in multiple and varied neurological symptoms and signs, usually with remissions and exacerbation. Recently, Kv1.3 channels have been proposed to be crucial in the pathogenesis of multiple sclerosis and other autoimmune diseases66,67. Myelin-reactive encephalitogenic rat T cells express high levels of Kv1.3 channels after repeated antigenic stimulation in vitro67. Adoptive transfer of these T cells into rats induces experimental autoimmune encephalomyelitis, which can be reversed by ShK. In humans, activated myelin-reactive T (TEM) cells from patients with multiple sclerosis express significantly higher levels of Kv1.3 channels than naive or central memory T cells, and Kv1.3 inhibitors such as ShK suppress proliferation of TEM cells68. Therefore, selective Kv1.3 inhibitors might represent an appropriate therapy for the treatment of autoimmune diseases such as multiple sclerosis, as well as perhaps type 1 diabetes, psoriasis and rheumatoid arthritis. The pharmacokinetic properties of ShK in different species are not known, and ways to deliver therapeutic concentrations of the peptide need to be considered. ShK is expected to produce similar side effects to MgTX, including effects on the enteric nervous system53. The potential central effects of ShK also need to be considered, because the blood–brain barrier could be compromised in autoimmune diseases.
Selective potassium-channel blockers might also have potential in the treatment of cancer, as human ether-a-go-go-related gene (hERG) K+ channels seem to be overexpressed in different tumours69,70. In this regard, the selectivity of ErgTx toxins71, BeKM-1 (Ref. 72) and APETx-1 (Ref. 73) for hERG K+ channels might have therapeutic implications.
Chloride-channel toxins. Chloride channels are also among the many membrane proteins overexpressed in different types of cancers. Chlorotoxin isolated from the scorpion Leiurus quinquestriatus74 binds to specific Ca2+-activated chloride channels75 and certain tumours and gliomas, and therefore might have potential in the treatment of cancer76. Although recent studies indicate that chlorotoxin inhibits matrix metalloproteinase 2, which is also upregulated in gliomas77, and might not be a general chloride-channel inhibitor78, the radioactive 131I-chlorotoxin analogue has cytolytic activity, and therefore the potential to selectively affect tumours and gliomas of neuroectodermal origin79,80. On the basis of these findings, TransMolecular Inc. is running trials with 131I-TM-601 (131I-chlorotoxin) as an investigational new drug for the treatment of gliomas.
Toxins inhibiting nicotinic acetylcholine receptors. The α-conotoxins are a rapidly growing class of small peptides that competitively inhibit nicotinic acetylcholine receptors (nAChRs). Similarly to the snake α-neurotoxins which have been intensively studied81, α-conotoxins bind at the interface between specific subunits, allowing them to discriminate among different nAChR subtypes82. Muscle-selective α-conotoxins (for example, α-GI, see Table 1) or miniproteins engineered from α-neurotoxins (Box 1) could represent an alternative to the use of small-molecule curare-mimetic muscle relaxants, which are used during surgery but have slower than ideal recovery periods83. As mentioned in the introduction, agonists of nAChRs function as analgesics. However, a novel α-conotoxin, Vc1.1, has been recently identified as having potential analgesic properties84.
Venom peptides for cardiovascular disease. The first example of a successful venom-based drug is captopril (Capoten; Anakena), which inhibits angiotensin-converting enzyme (ACE), an essential enzyme for the production of angiotensin, which is in turn a vasoconstrictor associated with hypertension. The route by which Cushman and Ondetti developed captopril at Bristol-Myers Squibb is described in Box 2. ACE inhibitors continue to be an important class of antihypertensive agents, despite the development of alternative pharmacologies85, such as B-type natriuretic peptides86, which are approved for use in acutely decompensated chronic heart failure. A stabilized synthetic form of the natriuretic peptide from the green mamba Dendroapsis augusticeps also seems to have therapeutic potential87.
Snake-venom peptides have since been used to guide the development of novel antithrombotics that act as competitive antagonists of the binding of ligand (for example, fibrinogen) to integrin αIIbβ3 on activated platelets. Among the most specific αIIbβ3 inhibitors is eptifibatide (Integrilin; Millennium Pharmaceuticals), a cyclic heptapeptide developed to mimic the high selectivity of barbourin88, a snake disintegrin that possesses a KDG motif, rather than the RGD motif found in other disintegrins89 and integrins90. Eptifibatide and the small-molecule RGD-mimetic tirofiban (Aggrastat; Merck)91 are both used clinically in intravenous formulations. Orally active αIIbβ3 antagonists with limited bioavailability have since been developed, but seem to be no more effective than widely used antiplatelet agents such as aspirin92. Ancrod from the venom of the Malayan pit viper Agkistrodon rhodostoma, and batroxobin from the venom of Bothrops atrox moojeni, enzymatically cleave blood fibrinogen93 and seem to reduce neurological deficits when used in the early stages of stroke94.
Snake venoms also contain peptides with antihaemorrhagic properties. These include textilinin, a novel antifibrinolytic serine protease inhibitor from common brown snake (Pseudonaja textilis) venom95 that is now in preclinical development as a novel anti-bleeding product for use in open-heart surgery (Q70033; QRxPharma). Many of the wide range of haemostatic factors found in snake venoms have been used in the development of laboratory diagnostics (for example, those produced by Pentapharm Ltd and Gradipore) to measure levels of fibrinogen, prothrombin, blood-clotting factors and protein C associated with haemostatic disorders.
Venom peptides might also prove useful in the development of novel treatments for hypertension (ρ-conopeptides) and atrial fibrillation (GsMTx-4). The ρ-conopeptides are selective, non-competitive inhibitors of the α1-adrenoceptor96,97. GsMTx-4 from the tarantula Grammostola spatulata98 is a novel blocker of mechanosensitive ion channels99 that inhibits atrial fibrillation100.
Noradrenaline transporter inhibitors. The noradrenaline transporter (NET) is important in reducing the concentration of neuronally released noradrenaline, and as a consequence influences learning and memory, as well as endocrine and autonomic functions101. Drugs that inhibit the NET have antidepressant and/or psychostimulant effects102, produce antinociception through the enhancement of descending inhibitory pathways in the spinal cord103, and might also be useful in the treatment of cardiovascular disorders and urinary incontinence104. The χ-conopeptides are highly specific, non-competitive inhibitors of noradrenaline uptake by human and rat NET96. The pharmacology of the χ-conopeptides was first identified in rat vas deferens contractility studies, which are sensitive to inhibition by NET96. Intrathecal χ-MrIA produces analgesia in a hot-plate assay105, and is more potent and efficacious than morphine in a rat chronic constriction injury model of neuropathic pain106. A variant of χ-MrIA (Xen2174), is being developed as a novel analgesic by Xenome Ltd. Interestingly, the binding site for χ-conopeptides on the NET partially overlaps the tricyclic antidepressant binding site107,108.
NMDA receptor antagonists. Conantokins are specific inhibitors of the NMDA receptor. They are helical peptides109,110 that competitively inhibit glutamate activation, especially at NR2B receptors111. Analogues of conantokin-G discriminate among different NMDA receptor subtypes in human brain112, and the anti-epileptic effects of the conantokins113 have been explored by Cognetix Inc. Reflecting the probable role of NMDA receptors in pain neuroplasticity, Malmberg et al.114 showed that intrathecal conantokin-G and -T also have analgesic activity in pain models of tissue damage (formalin test), nerve injury (partial sciatic nerve ligation) and inflammation (complete Freund's adjuvant) in mice at doses that were ∼20-fold lower than those required to impair motor function. So, subtype-specific inhibitors of the NMDA receptor also have therapeutic potential in the management of pain. Further studies are required to determine whether subtype-specific inhibitors of NMDA receptors are devoid of central adverse effects, including effects on memory and learning.
Neurotensin receptor agonists. Cone snails produce a glycosylated neurotensin analogue named contulakin-G115 that is a potent analgesic in a wide range of animal models of pain116. Interestingly, contulakin-G is 100-fold less potent than neurotensin for neurotensin receptor 1 (NTSR1), but ∼100-fold more potent as an analgesic, indicating an additional mechanism(s) of action besides the neurotensin receptor. On the basis of its potency and wide therapeutic window, contulakin-G (CGX-1160) is in early stage clinical development by Cognetix for the treatment of pain.
Venom peptides useful in diabetes. Glucagon-like peptide-1 (GLP1) is an insulinotropic hormone secreted from endocrine cells of the small and large intestine in a nutrient-dependent manner. GLP-1 inhibits gastric emptying and food intake, and controls blood glucose levels. A GLP-related peptide, exendin-4 from the venom of the Gila monster Heloderma suspectum117, has been shown to be active in vivo118. On the basis of this activity, exendin-4 (Exenatide; Amylin Pharmaceuticals) is presently in Phase III clinical trials for the treatment of type 2 diabetes. Surprisingly, GLP-related peptides, including exendin-4, share structural homology to α-latrotoxin from the black widow spider119 and might have potential in the treatment of Alzheimer's disease120.
As a consequence of their high selectivity, venom peptides have proved particularly useful for in vitro and in vivo proof-of-concept studies. However, for therapeutic applications, a number of issues associated with safety, pharmacokinetics and delivery need to be addressed. Optimization of peptide delivery to peripheral and central targets will help to determine whether or not these peptides can be considered candidates for drug development. Peptides that block channels by altering the gating mechanism might have potential to become selective potassium-channel inhibitors, whereas pore-blocking toxins could be designed to be selective inhibitors of subtypes of sodium channels. It remains to be determined how many of the peptides that are present in venoms can find a clinical utility.
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We thank Iain Sharpe, Christina Schroeder, Sebastien Dutertre and Alun Jones for help in preparing the figures. Supported by grants from the NHMRC and ARC, Australia.
Online Mendelian Inheritance in Man
Unicellular algae that produce a range of toxins that enter the food chain during blooms.
- ENVENOMATION APPARATUS
Highly specialized glands secreting peptides injected via hollow teeth, stings, harpoons and nematocyst tubules.
- YUCATAN MINI-PIG
Yucatan mini-pigs are used experimentally because their immune system resembles the human situation.
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