Abstract
Skeletal muscle necrosis is a common clinical manifestation of snakebite envenoming. The predominant myotoxic components in snake venoms are catalytically-active phospholipases A2 (PLA2) and PLA2 homologs devoid of enzymatic activity, which have been used as models to investigate various aspects of muscle degeneration. This review addresses the changes in the contractile apparatus of skeletal muscle induced by these toxins. Myotoxic components initially disrupt the integrity of sarcolemma, generating a calcium influx that causes various degenerative events, including hypercontraction of myofilaments. There is removal of specific sarcomeric proteins, owing to the hydrolytic action of muscle calpains and proteinases from invading inflammatory cells, causing an initial redistribution followed by widespread degradation of myofibrillar material. Experiments using skinned cardiomyocytes and skeletal muscle fibers show that these myotoxins do not directly affect the contractile apparatus, implying that hypercontraction is due to cytosolic calcium increase secondary to sarcolemmal damage. Such drastic hypercontraction may contribute to muscle damage by generating mechanical stress and further sarcolemmal damage.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
Skeletal muscle degeneration occurs in a variety of pathologies that include genetic disorders, e.g., Duchenne muscular dystrophy and other dystrophies (Saini-Chohan et al. 2012; Bargui et al. 2021), ischemia reperfusion injury (Gillani et al. 2012), cachexia (Ali and Garcia 2014), and toxic damage induced by synthetic and natural compounds (Nagahama et al. 2019; Janssen et al. 2020). Local and systemic muscle degeneration are characteristic of envenomings by a variety of snakes of the families Viperidae and Elapidae (Warrell 2010; Gutierrez et al. 2017). Local myonecrosis induced by viperid species is often associated with other tissue alterations, including vascular damage, edema, nerve damage, and blistering, and may lead to permanent tissue loss and dysfunction (Gutierrez et al. 2009). In turn, systemic myotoxicity, i.e., rhabdomyolysis, is observed in envenomings by some elapid and few viperid species. Such widespread muscle breakdown is associated with myoglobinuria, hyperkalemia, and acute kidney injury (Azevedo-Marques et al. 1985; Gutierrez et al. 2017; Johnston et al. 2022).
Snake venom-induced myotoxicity is due to the action of a variety of venom components, mainly secreted phospholipase A2 (PLA2) enzymes, PLA2 homologs devoid of enzymatic activity, matrix-degrading metalloproteinases, and a group of low molecular mass myotoxins having homology with β-defensins (Harris and Cullen 1990; Gutierrez and Ownby 2003; Lomonte 2023). By far, the most important myotoxic components in snake venoms are PLA2s and PLA2 homologs (Gutierrez and Ownby 2003; Lomonte and Križaj 2021). Since these toxins induce a synchronous pattern of muscle damage, they have become useful tools for studying the cellular processes involved in skeletal muscle degeneration and regeneration (Harris and Cullen 1990; Harris 2003). In particular, myotoxic PLA2s and PLA2 homologs from the venoms of the species Bothrops asper (family Viperidae, group II secreted PLA2s) and Notechis scutatus (family Elapidae, group I secreted PLA2s) have been extensively used in these investigations, although studies with other similar toxins have been also carried out (Dixon and Harris 1996; Gutierrez and Ownby 2003; Lomonte 2023). Some of these myotoxins are catalytically-active Asp-49 enzymes that cleave the sn-2 ester bond in phospholipids, while PLA2 homologs (also referred to as PLA2-like myotoxins) display mutations in residue 49 and other residues of the so-called calcium-binding loop, thus rendering these proteins enzymatically inactive, although keeping the ability to damage muscle fibers (Francis et al. 1991; Ward et al. 2002; Gutierrez and Ownby 2003; Lomonte and Rangel 2012).
The mechanism of action of myotoxic PLA2s and PLA2 homologs has been investigated by using a variety of experimental models (rodent in vivo tests, ex vivo muscle preparations and isolated cells, intravital microscopy, cell culture models, and phospholipid vesicles) (Dixon and Harris 1996; Gutierrez and Ownby 2003; Lomonte 2023). These investigations have shown that the first stage in the action of these toxins is the binding to the skeletal muscle plasma membrane, followed by the disruption of the integrity of muscle sarcolemma, either by enzymatic degradation of phospholipids or by a catalytically-independent destabilization of the membrane (Dixon and Harris 1996; Fernandez et al. 2013; Fernandes et al. 2014). The identity of the membrane receptors for these toxins remains largely unknown, although some candidates have been proposed (reviewed in Lomonte and Križaj (2021)).
This initial sarcolemmal destabilization leads to loss of ion gradients and depolarization (Harris et al. 2003; Melo et al. 2004), as well as to the release of muscle cytosolic enzymes, such as creatine kinase and aspartate aminotransferase (Gutierrez et al. 1984a; Preston et al. 1990). A key event in these early stages of cell damage is a prominent influx of calcium following the steep concentration gradient across the sarcolemma (Gutierrez et al. 1984a; Villalobos et al. 2007; Cintra-Francischinelli et al. 2009). The consequent increase in cytosolic calcium concentration promotes a complex series of intracellular degenerative events, such as mitochondrial degeneration, activation of calcium-dependent proteinases and cytosolic PLA2s, degradation of intracellular membranes, and hypercontraction of myofilaments, which bring the cell beyond the point-of-no-return and necrosis (Gutierrez et al. 1984b; Gutierrez and Ownby 2003; Harris et al. 2003; Montecucco et al. 2008). This minireview describes the main alterations of the contractile apparatus of muscle fibers as a consequence of the action of venom myotoxic PLA2s and PLA2 homologs. Further, it highlights some possible experimental strategies to be explored with the aim of reducing muscle damage, by selectively targeting key elements of the contractile mechanism.
A prominent early alteration in myofibrillar structure is characteristic of myonecrosis induced by venom PLA2s and PLA2 homologues
Within minutes of injection of these myotoxic components in mice or rats, there is histological evidence of myofilament hypercontraction, as revealed by the formation of dense myofibrillar aggregates in the cytoplasm, leaving spaces devoid of myofibrils (Gutierrez et al. 1984b, 1991; Johnson and Ownby 1993; Harris et al. 2003). Such notorious histological change is used to estimate the fraction of fibers affected by the venom, i.e., the necrotic index, as a quantitative indicator of the myotoxic activity of venoms or toxins (Teixeira et al. 2003). At the ultrastructural level, dense amorphous masses of filaments are formed, alternating with spaces devoid of myofibrillar material. Sarcomeres are shortened and there is misalignment between Z lines (Dixon and Harris 1996; Harris et al. 2003). In other regions, the characteristic structural organization of the sarcomeres is completely lost (Gutierrez et al. 1984b; Dixon and Harris 1996). The hypercontracted masses can be also observed by scanning electron microscopy (Dixon and Harris 1996). Ultrastructural observations in muscle affected by PLA2-rich myotoxic venom and by purified myotoxins revealed that the plasma membrane was disrupted in areas showing hypercontraction of myofilaments (Gutierrez et al. 1984b; Dixon and Harris 1996). Histologically, these areas present ‘delta lesions’. i.e., wedge-shaped lesions associated with myofilament hypercontraction (Gutierrez et al. 1984b, 1989, 1991). This can be interpreted in the light of the early damage to the sarcolemma, generating a calcium influx that induces hypercontraction.
The dynamics of this hypercontraction process was studied by intravital microscopy by applying the venom of Bothrops asper and a myotoxin to the mouse cremaster muscle (Lomonte et al. 1994). Early muscle fiber contractions were followed, 3 to 4 min after application of the myotoxic agents, by the focal loss of striations and a slow retraction of myofibrils in opposite directions, generating a row of hypercontracted material alternating with empty spaces within the cells. Electron microscopic evidence shows numerous foci of hypercontracted myofibrils in a single muscle fiber (Dixon and Harris 1996).
Does hypercontraction amplify sarcolemmal damage and necrosis?
Electron microscopic observations highlighted that the integrity of sarcolemma is interrupted in regions with hypercontracted myofibrils after injection of myotoxic PLA2s (Gutierrez et al. 1984b; Dixon and Harris 1996). This can be interpreted in two ways: (a) the toxins initially affect the integrity of the sarcolemma, causing a calcium influx that promotes hypercontraction, or (b) hypercontraction of myofilaments generates a mechanical stress that disrupts the sarcolemma (Dixon and Harris 1996). These possibilities are not exclusive, since an initial toxin-mediated disruption of the sarcolemma would induce a calcium influx, causing hypercontraction which, in turn, may generate mechanical stress in undamaged sarcolemma, causing its disruption, hence expanding fiber damage, a hypothesis that needs to be explored experimentally.
Alterations in specific components of the myofibrils along the degenerative process
Immunohistochemical and immunochemical studies have addressed the changes in the immunostaining of several myofibrillar proteins along the course of the PLA2-induced degenerative events. There is an early loss of desmin immunostaining in necrotic fibers (Gutierrez et al. 1990; Harris et al. 2003). Desmin locates peripherally to Z discs and plays a key role in the structural and mechanical integrity of the contractile apparatus (Lazarides 1980; Paulin and Li 2004; Sweeney and Hammers 2018). Thus, desmin loss is likely to be associated with the overall disorganization of the contractile apparatus. In agreement, the degeneration of Z lines correlated with the loss of the immunostaining of desmin in muscle injected with a myotoxic venom (Vater et al. 1992). Loss of immunostaining for desmin was used to identify areas of muscle damage in venom-injected muscle (de Oliveira et al. 2023). Immunostaining of other myofibrillar proteins, i.e., α-actinin and titin, is reduced or lost at later time intervals (between 3 and 7 h), as well as dystrophin staining (Gutierrez et al. 1990; Harris et al. 2003). Likewise, staining of β-dystroglycan is affected at later time intervals, i.e., 12 h, in necrotic fibers (Vater et al. 1995). These alterations are likely to contribute to the overall disorganization of myofibrillar structure and to the loss of integration of myofibrils with the plasma membrane. In particular, the loss of α-actinin is likely to play a key role in such disorganization (Gutierrez et al. 1990).
A shift in the ultrastructure of hypercontracted masses occurs as a consequence of the action of muscle proteinases
Histological and ultrastructural observations in skeletal muscle affected by a myotoxic PLA2 highlight a change in the morphology of hypercontracted myofilament masses in necrotic fibers. By 3 h and afterwards a more uniform distribution of the disorganized myofibrillar material is observed. Instead of being formed by dense hypercontracted masses alternating with spaces devoid of myofibrillar material, this material becomes more uniformly distributed in the cellular space (Gutierrez et al. 1984b, 1990). In the case of myonecrosis induced by B. asper myotoxic PLA2, such shift in myofibrillar material correlates with the loss of immunostaining of α-actinin (Gutierrez et al. 1990). α-actinin is located at the Z disc and contributes to the formation of a lattice-like structure that provides stability and integration to the contractile machinery (Sjoblom et al. 2008). Owing to the role of this protein in the mechanical integration of myofibrillar contraction, it was suggested that the redistribution of myofibrillar material is likely to be due to degradation of α-actinin, which occurs after loss of desmin. Noteworthy, when this structural shift occurs, there is no overt degradation of actin and myosin, the main components of the contractile apparatus (Gutierrez et al. 1986, 1990).
Such selective hydrolysis of key myofibrillar components, such as desmin and α-actinin, is likely due to the action of calpains, a group of cytosolic calcium-dependent cysteine proteinases that play a key role in protein turnover (Hyatt and Powers 2020). Calpains are activated by the increase in cytosolic calcium concentration in myotoxin-induced necrosis following plasma membrane disruption. Calpain-1 is known to cleave desmin in muscle atrophy (Aweida et al. 2018; Cohen 2020).
Degradation of actin and myosin occurs at a later stage and is mostly mediated by proteinases from invading phagocytic cells
In contrast to desmin, titin and α-actinin, the degradation of actin and myosin occurs later on in the course of the unfolding of degenerative events in skeletal muscle fibers affected by myotoxic venoms and PLA2s (Gutierrez et al. 1986, 1990; Abul Faiz et al. 1995). In the case of necrosis due to B. asper venom and myotoxic PLA2, SDS-PAGE analysis of muscle proteins indicates that reduction in the intensity of bands having the molecular masses of actin and myosin occurred mainly after 24 h of the onset of necrosis (Gutierrez et al. 1986, 1990). This coincides with the time-course of the arrival of neutrophils and macrophages to the necrotic tissue, thus suggesting that such degradation is due to the action of lysosomal proteinases of these inflammatory cells (Gutierrez et al. 1986, 1990). This pattern of myofibrillar protein degradation fits within the ‘two step’ model proposed by Ishiura et al. (1984) for muscle degeneration induced by plasmocid, in which the early loss of α-actinin is mediated by cytosolic muscle calcium-dependent proteinases, while the degradation of actin and myosin depends on the action of proteinases from invading inflammatory cells. Figure 1 summarizes the main events occurring in the contractile apparatus of skeletal muscle fibers as a consequence of the action of myotoxic PLA2s and PLA2 homologs.
Do myotoxic PLA2s and PLA2 homologs have a direct action on the intracellular structures of skeletal muscle?
Although a large body of experimental evidence indicates that the sarcolemma is the primary site of action of snake venom myotoxic PLA2s and PLA2 homologs, more recent observations show intracellular localization of these toxins in myotubes in culture and in muscle cells in vivo (Massimino et al. 2018; Vargas-Valerio et al. 2021). Whether this occurs by endocytosis or secondary to sarcolemmal disruption remains to be assessed. Interestingly, a PLA2 homolog from B. asper venom binds and colocalizes in myotubes with nucleolin, a nucleolar protein that is also present on the cell surface, and also pulls down this protein in extracts of membranes obtained from ex vivo skeletal muscle preparations (Massimino et al. 2018). Furthermore, this binding is relevant to the cytotoxic action of this myotoxin since nucleolin antagonists inhibit toxin internalization and cytotoxicity (Massimino et al. 2018). Thus, myotoxins can reach the intracellular space by diverse mechanisms and might affect intracellular structures and processes as part of their mechanism of action. For instance, a myotoxic PLA2 from B. asper venom inhibits Ca2+ ATPase and hydrolyzes phospholipids of rabbit skeletal muscle sarcoplasmic reticulum in vitro (Gutierrez et al. 1987). We have recently explored whether myotoxic PLA2 and PLA2 homolog from B. asper venom affect the contractile apparatus of skeletal muscle. The main results of these studies are summarized in the next section.
Studies on skinned muscle preparations and future research
The recent finding that PLA2 myotoxins can be internalized into muscle cells (Massimino et al. 2018; Vargas-Valerio et al. 2021), together with the above-mentioned hypercontraction, loss of striation and loss of immunostaining for some sarcomeric proteins observed after injection of myotoxins in animal models, has raised new questions to further elucidate their mechanisms of action. Once inside the sarcoplasm, do PLA2 myotoxins interact with sarcomeric proteins?; do they alter the structure and mechanical properties of myofilaments?; do they directly or indirectly modify the mechanisms of force generation or relaxation? To investigate these possibilities, we followed a reductionist strategy (i.e., removing the cell membrane and studying the effect of myotoxins in skinned muscle preparations compared to intact tissue; see Batters et al. 2014; Kalakoutis et al. 2021; Lewalle et al. 2022). In parallel, we tested the effect of small molecules (i.e., myosin inhibitors; see Rauscher et al. 2018; Marston 2019) on toxin-induced hypercontraction. The combined use of these tools allows us to dissect the effects of myotoxins at key events in excitation–contraction coupling (Dirksen et al. 2022). The main results to date obtained from these efforts are briefly described below.
In a first study (Lopez-Davila et al. 2021), single rat cardiomyocytes were used as an ex vivo experimental model. Although cardiomyocytes are not the main target of these toxins in envenomings, our growing understanding of the structural, functional and pathological similarities and differences between skeletal and cardiac muscle makes cardiomyocytes a useful model to explore the mechanism of action of myotoxins (Saini-Chohan et al. 2012; Henderson et al. 2017; Sweeney and Hammers 2018; Bargui et al. 2021; Glancy and Balaban 2021). In single intact cardiomyocytes, the Lys49 PLA2 homolog Mt-II, from B. asper venom, induced disruption of the plasma membrane and increased intracellular calcium concentrations, calcium transient amplitudes, and unloaded cell shortening. Over time, these changes typically lead to irreversible hypercontraction in a dose-dependent manner (i.e., time to hypercontraction was inversely proportional to toxin concentration, on a timescale of few minutes). On the other hand, Mt-II did not alter key parameters of force development in skinned, isometrically held single cardiomyocytes, as cooperativity, rate constant and calcium sensitivity of active force development and maximal active and passive force did not differ from control measurements. Interestingly, the irreversible hypercontraction observed in intact cardiomyocytes was reversed by the myosin inhibitor para-Aminoblebbistatin (AmBleb (Varkuti et al. 2016)). This opens the possibility of using small molecular inhibitors to modulate this aspect of toxin-induced cytotoxicity (Lopez-Davila et al. 2021).
In a subsequent study, we extended these observations to skeletal muscle preparations (a primary target of myotoxins), using both catalytically-active PLA2 (Mt-I) and inactive PLA2 homolog (Mt-II). Essentially, the irreversible hypercontraction observed in intact cardiomyocytes was readily reproduced after treatment with either Mt-I or Mt-II in myotubes differentiated in vitro from mouse C2C12 myoblasts. As observed for skinned cardiomyocytes, the toxins did not affect the main parameters of force development measured in single, isometrically held rabbit psoas skinned fibers (Lopez-Davila et al. 2023). The results of these studies are summarized in Fig. 2.
Studying the effects of myotoxins in skinned muscle preparations allows screening for possible effects on the full spectrum of sarcomeric proteins, thus avoiding effects that depend on sarcolemmal disruption. An additional advantage of this strategy is the access to the broadly conserved sarcomere assembly of this preparation, which is important for both the biochemistry and function of sarcomeric proteins (Lewalle et al. 2022). The lack of effect at this level implies that further elaboration of the reductionist approach, e.g., by applying myotoxins to isolated sarcomeric proteins, would not be relevant. On the other hand, the fact that the myosin inhibitor abolished hypercontraction in intact cardiomyocytes calls for its use to further explore the role of hypercontraction in the overall cell damage induced by these toxins.
As mentioned above, it has been hypothesized that myotoxins induce a high contractile force as a consequence of calcium influx, which in turn could cause mechanical damage of sarcolemma and other cellular structures, which would expand the process of cell degeneration. This raises the possibility of testing whether compounds targeting key sarcomeric proteins (e.g., myosin inhibitors or troponin modulators) would reduce the extent of muscle damage as a possible therapeutic tool. This can be addressed by using some of the methods described in this review, such as myotube cell culture, as well as ex vivo and in vivo models. Furthermore, experiments on intact, loaded muscle preparations could generate worthwhile insight. Targeting the sarcomeric proteins to correct muscle function at the level of the crossbridge cycle, as currently intended for cardiac and skeletal myopathies (Hwang and Sykes 2015), could become an emerging strategy for dealing with snake venom-induced skeletal muscle necrosis, a hypothesis that needs to be evaluated.
Data availability
Not applicable.
References
Abul Faiz M, Harris JB, Maltin CA, Mantle D (1995) Comparison of structural protein and proteolytic enzyme levels in degenerating and regenerating rat muscle induced by Notechis scutatus venom. Comp Biochem Physiol B 110:241–253. https://doi.org/10.1016/0305-0491(94)00128-h
Ali S, Garcia JM (2014) Sarcopenia, cachexia and aging: diagnosis, mechanisms and therapeutic options—a mini-review. Gerontology 60:294–305. https://doi.org/10.1159/000356760
Aweida D, Rudesky I, Volodin A, Shimko E, Cohen S (2018) GSK3-beta promotes calpain-1-mediated desmin filament depolymerization and myofibril loss in atrophy. J Cell Biol 217:3698–3714. https://doi.org/10.1083/jcb.201802018
Azevedo-Marques MM, Cupo P, Coimbra TM, Hering SE, Rossi MA, Laure CJ (1985) Myonecrosis, myoglobinuria and acute renal failure induced by South American rattlesnake (Crotalus durissus terrificus) envenomation in Brazil. Toxicon 23:631–636. https://doi.org/10.1016/0041-0101(85)90367-8
Bargui R, Solgadi A, Prost B, Chester M, Ferreiro A, Piquereau J, Moulin M (2021) Phospholipids: identification and implication in muscle pathophysiology. Int J Mol Sci. https://doi.org/10.3390/ijms22158176
Batters C, Veigel C, Homsher E, Sellers JR (2014) To understand muscle you must take it apart. Front Physiol 5:90. https://doi.org/10.3389/fphys.2014.00090
Cintra-Francischinelli M, Pizzo P, Rodrigues-Simioni L, Ponce-Soto LA, Rossetto O, Lomonte B, Gutierrez JM, Pozzan T, Montecucco C (2009) Calcium imaging of muscle cells treated with snake myotoxins reveals toxin synergism and presence of acceptors. Cell Mol Life Sci 66:1718–1728. https://doi.org/10.1007/s00018-009-9053-2
Cohen S (2020) Role of calpains in promoting desmin filaments depolymerization and muscle atrophy. Biochim Biophys Acta Mol Cell Res 1867:118788. https://doi.org/10.1016/j.bbamcr.2020.118788
de Oliveira AK, Pramoonjago P, Rucavado A, Moskaluk C, Silva DT, Escalante T, Gutierrez JM, Fox JW (2023) Mapping the immune cell microenvironment with spatial profiling in muscle tissue injected with the venom of Daboia russelii. Toxins (basel). https://doi.org/10.3390/toxins15030208
Dirksen RT, Eisner DA, Rios E, Sipido KR (2022) Excitation-contraction coupling in cardiac, skeletal, and smooth muscle. J Gen Physiol. https://doi.org/10.1085/jgp.202213244
Dixon RW, Harris JB (1996) Myotoxic activity of the toxic phospholipase, notexin, from the venom of the Australian tiger snake. J Neuropathol Exp Neurol 55:1230–1237. https://doi.org/10.1097/00005072-199612000-00006
Fernandes CA, Borges RJ, Lomonte B, Fontes MR (2014) A structure-based proposal for a comprehensive myotoxic mechanism of phospholipase A2-like proteins from viperid snake venoms. Biochim Biophys Acta 1844:2265–2276. https://doi.org/10.1016/j.bbapap.2014.09.015
Fernandez J, Caccin P, Koster G, Lomonte B, Gutierrez JM, Montecucco C, Postle AD (2013) Muscle phospholipid hydrolysis by Bothrops asper Asp49 and Lys49 phospholipase A(2) myotoxins–distinct mechanisms of action. FEBS J 280:3878–3886. https://doi.org/10.1111/febs.12386
Francis B, Gutierrez JM, Lomonte B, Kaiser II (1991) Myotoxin II from Bothrops asper (Terciopelo) venom is a lysine-49 phospholipase A2. Arch Biochem Biophys 284:352–359. https://doi.org/10.1016/0003-9861(91)90307-5
Gillani S, Cao J, Suzuki T, Hak DJ (2012) The effect of ischemia reperfusion injury on skeletal muscle. Injury 43:670–675. https://doi.org/10.1016/j.injury.2011.03.008
Glancy B, Balaban RS (2021) Energy metabolism design of the striated muscle cell. Physiol Rev 101:1561–1607. https://doi.org/10.1152/physrev.00040.2020
Gutierrez JM, Ownby CL (2003) Skeletal muscle degeneration induced by venom phospholipases A2: insights into the mechanisms of local and systemic myotoxicity. Toxicon 42:915–931. https://doi.org/10.1016/j.toxicon.2003.11.005
Gutierrez JM, Ownby CL, Odell GV (1984a) Isolation of a myotoxin from Bothrops asper venom: partial characterization and action on skeletal muscle. Toxicon 22:115–128. https://doi.org/10.1016/0041-0101(84)90144-2
Gutierrez JM, Ownby CL, Odell GV (1984b) Pathogenesis of myonecrosis induced by crude venom and a myotoxin of Bothrops asper. Exp Mol Pathol 40:367–379. https://doi.org/10.1016/0014-4800(84)90054-6
Gutierrez JM, Chaves F, Cerdas L (1986) Inflammatory infiltrate in skeletal muscle injected with Bothrops asper venom. Rev Biol Trop 34:209–214
Gutierrez JM, Rojas G, Lomonte B, Gene JA, Cerdas L (1987) Effects of a myotoxic phospholipase A2 isolated from Bothrops asper venom on skeletal muscle sarcoplasmic reticulum. Toxicon 25:1244–1248. https://doi.org/10.1016/0041-0101(87)90144-9
Gutierrez JM, Chaves F, Gene JA, Lomonte B, Camacho Z, Schosinsky K (1989) Myonecrosis induced in mice by a basic myotoxin isolated from the venom of the snake Bothrops nummifer (jumping viper) from Costa Rica. Toxicon 27:735–745. https://doi.org/10.1016/0041-0101(89)90040-8
Gutierrez JM, Arce V, Brenes F, Chaves F (1990) Changes in myofibrillar components after skeletal muscle necrosis induced by a myotoxin isolated from the venom of the snake Bothrops asper. Exp Mol Pathol 52:25–36. https://doi.org/10.1016/0014-4800(90)90055-i
Gutierrez JM, Nunez J, Diaz C, Cintra AC, Homsi-Brandeburgo MI, Giglio JR (1991) Skeletal muscle degeneration and regeneration after injection of bothropstoxin-II, a phospholipase A2 isolated from the venom of the snake Bothrops jararacussu. Exp Mol Pathol 55:217–229. https://doi.org/10.1016/0014-4800(91)90002-f
Gutierrez JM, Rucavado A, Chaves F, Diaz C, Escalante T (2009) Experimental pathology of local tissue damage induced by Bothrops asper snake venom. Toxicon 54:958–975. https://doi.org/10.1016/j.toxicon.2009.01.038
Gutierrez JM, Calvete JJ, Habib AG, Harrison RA, Williams DJ, Warrell DA (2017) Snakebite envenoming. Nat Rev Dis Primers 3:17079. https://doi.org/10.1038/nrdp.2017.79
Harris JB (2003) Myotoxic phospholipases A2 and the regeneration of skeletal muscles. Toxicon 42:933–945. https://doi.org/10.1016/j.toxicon.2003.11.011
Harris JB, Cullen MJ (1990) Muscle necrosis caused by snake venoms and toxins. Electron Microsc Rev 3:183–211. https://doi.org/10.1016/0892-0354(90)90001-9
Harris JB, Vater R, Wilson M, Cullen MJ (2003) Muscle fibre breakdown in venom-induced muscle degeneration. J Anat 202:363–372. https://doi.org/10.1046/j.1469-7580.2003.00171.x
Henderson CA, Gomez CG, Novak SM, Mi-Mi L, Gregorio CC (2017) Overview of the muscle cytoskeleton. Compr Physiol 7:891–944. https://doi.org/10.1002/cphy.c160033
Hwang PM, Sykes BD (2015) Targeting the sarcomere to correct muscle function. Nat Rev Drug Discov 14:313–328. https://doi.org/10.1038/nrd4554
Hyatt HW, Powers SK (2020) The role of calpains in skeletal muscle remodeling with exercise and inactivity-induced atrophy. Int J Sports Med 41:994–1008. https://doi.org/10.1055/a-1199-7662
Ishiura S, Nonaka I, Nakase H, Tada A, Sugita H (1984) Two-step mechanism of myofibrillar protein degradation in acute plasmocid-induced muscle necrosis. Biochim Biophys Acta 798:333–342. https://doi.org/10.1016/0304-4165(84)90107-7
Janssen L, Allard NAE, Saris CGJ, Keijer J, Hopman MTE, Timmers S (2020) Muscle toxicity of drugs: when drugs turn physiology into pathophysiology. Physiol Rev 100:633–672. https://doi.org/10.1152/physrev.00002.2019
Johnson EK, Ownby CL (1993) Isolation of a myotoxin from the venom of Agkistrodon contortrix laticinctus (broad-banded copperhead) and pathogenesis of myonecrosis induced by it in mice. Toxicon 31:243–255. https://doi.org/10.1016/0041-0101(93)90143-7
Johnston CI, Tasoulis T, Isbister GK (2022) Australian Sea Snake Envenoming causes myotoxicity and non-specific systemic symptoms—Australian Snakebite Project (ASP-24). Front Pharmacol 13:816795. https://doi.org/10.3389/fphar.2022.816795
Kalakoutis M, Di Giulio I, Douiri A, Ochala J, Harridge SDR, Woledge RC (2021) Methodological considerations in measuring specific force in human single skinned muscle fibres. Acta Physiol (oxf) 233:e13719. https://doi.org/10.1111/apha.13719
Lazarides E (1980) Intermediate filaments as mechanical integrators of cellular space. Nature 283:249–256. https://doi.org/10.1038/283249a0
Lewalle A, Campbell KS, Campbell SG, Milburn GN, Niederer SA (2022) Functional and structural differences between skinned and intact muscle preparations. J Gen Physiol. https://doi.org/10.1085/jgp.202112990
Lomonte B (2023) Lys49 myotoxins, secreted phospholipase A(2)-like proteins of viperid venoms: a comprehensive review. Toxicon 224:107024. https://doi.org/10.1016/j.toxicon.2023.107024
Lomonte B, Križaj I (2021) Snake venom phospholipase A2 toxins. In: Mackessy SP (ed) Handbook of venoms and toxins of reptiles, 2nd edn. CRC Press, Boca Raton, pp 389–411
Lomonte B, Rangel J (2012) Snake venom Lys49 myotoxins: from phospholipases A(2) to non-enzymatic membrane disruptors. Toxicon 60:520–530. https://doi.org/10.1016/j.toxicon.2012.02.007
Lomonte B, Lundgren J, Johansson B, Bagge U (1994) The dynamics of local tissue damage induced by Bothrops asper snake venom and myotoxin II on the mouse cremaster muscle: an intravital and electron microscopic study. Toxicon 32:41–55. https://doi.org/10.1016/0041-0101(94)90020-5
Lopez-Davila AJ, Weber N, Kraft T, Matinmehr F, Arias-Hidalgo M, Fernandez J, Lomonte B, Gutierrez JM (2021) Cytotoxicity of snake venom Lys49 PLA2-like myotoxin on rat cardiomyocytes ex vivo does not involve a direct action on the contractile apparatus. Sci Rep 11:19452. https://doi.org/10.1038/s41598-021-98594-5
Lopez-Davila AJ, Weber N, Nayak A, Fritz L, Moustafa KR, Gand LV, Wehry E, Kraft T, Thum T, Fernandez J, Gutierrez JM, Lomonte B (2023) Skeletal muscle fiber hypercontraction induced by Bothrops asper myotoxic phospholipases A(2) ex vivo does not involve a direct action on the contractile apparatus. Pflugers Arch. https://doi.org/10.1007/s00424-023-02840-w
Marston S (2019) Small molecule studies: the fourth wave of muscle research. J Muscle Res Cell Motil 40:69–76. https://doi.org/10.1007/s10974-019-09526-w
Massimino ML, Simonato M, Spolaore B, Franchin C, Arrigoni G, Marin O, Monturiol-Gross L, Fernandez J, Lomonte B, Tonello F (2018) Cell surface nucleolin interacts with and internalizes Bothrops asper Lys49 phospholipase A(2) and mediates its toxic activity. Sci Rep 8:10619. https://doi.org/10.1038/s41598-018-28846-4
Melo PA, Burns CF, Blankemeyer JT, Ownby CL (2004) Membrane depolarization is the initial action of crotoxin on isolated murine skeletal muscle. Toxicon 43:111–119. https://doi.org/10.1016/j.toxicon.2003.10.029
Montecucco C, Gutierrez JM, Lomonte B (2008) Cellular pathology induced by snake venom phospholipase A2 myotoxins and neurotoxins: common aspects of their mechanisms of action. Cell Mol Life Sci 65:2897–2912. https://doi.org/10.1007/s00018-008-8113-3
Nagahama M, Takehara M, Rood JI (2019) Histotoxic clostridial infections. Microbiol Spectr. https://doi.org/10.1128/microbiolspec.GPP3-0024-2018
Paulin D, Li Z (2004) Desmin: a major intermediate filament protein essential for the structural integrity and function of muscle. Exp Cell Res 301:1–7. https://doi.org/10.1016/j.yexcr.2004.08.004
Preston SA, Davis CE, Harris JB (1990) The assessment of muscle fibre loss after the injection of the venom of Notechis scutatus (Australian tiger snake). Toxicon 28:201–214. https://doi.org/10.1016/0041-0101(90)90414-3
Rauscher AA, Gyimesi M, Kovacs M, Malnasi-Csizmadia A (2018) Targeting myosin by blebbistatin derivatives: optimization and pharmacological potential. Trends Biochem Sci 43:700–713. https://doi.org/10.1016/j.tibs.2018.06.006
Saini-Chohan HK, Mitchell RW, Vaz FM, Zelinski T, Hatch GM (2012) Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: thematic review series: genetics of human lipid diseases. J Lipid Res 53:4–27. https://doi.org/10.1194/jlr.R012120
Sjoblom B, Salmazo A, Djinovic-Carugo K (2008) Alpha-actinin structure and regulation. Cell Mol Life Sci 65:2688–2701. https://doi.org/10.1007/s00018-008-8080-8
Sweeney HL, Hammers DW (2018) Muscle contraction. Cold Spring Harb Perspect Biol. https://doi.org/10.1101/cshperspect.a023200
Teixeira CF, Zamuner SR, Zuliani JP, Fernandes CM, Cruz-Hofling MA, Fernandes I, Chaves F, Gutierrez JM (2003) Neutrophils do not contribute to local tissue damage, but play a key role in skeletal muscle regeneration, in mice injected with Bothrops asper snake venom. Muscle Nerve 28:449–459. https://doi.org/10.1002/mus.10453
Vargas-Valerio S, Robleto J, Chaves-Araya S, Monturiol-Gross L, Lomonte B, Tonello F, Fernandez J (2021) Localization of Myotoxin I and Myotoxin II from the venom of Bothrops asper in a murine model. Toxicon 197:48–54. https://doi.org/10.1016/j.toxicon.2021.04.006
Varkuti BH, Kepiro M, Horvath IA, Vegner L, Rati S, Zsigmond A, Hegyi G, Lenkei Z, Varga M, Malnasi-Csizmadia A (2016) A highly soluble, non-phototoxic, non-fluorescent blebbistatin derivative. Sci Rep 6:26141. https://doi.org/10.1038/srep26141
Vater R, Cullen MJ, Harris JB (1992) The fate of desmin and titin during the degeneration and regeneration of the soleus muscle of the rat. Acta Neuropathol 84:278–288. https://doi.org/10.1007/BF00227821
Vater R, Harris JB, Anderson VB, Roberds SL, Campbell KP, Cullen MJ (1995) The expression of dystrophin-associated glycoproteins during skeletal muscle degeneration and regeneration. an immunofluorescence study. J Neuropathol Exp Neurol 54:557–569. https://doi.org/10.1097/00005072-199507000-00010
Villalobos JC, Mora R, Lomonte B, Gutierrez JM, Angulo Y (2007) Cytotoxicity induced in myotubes by a Lys49 phospholipase A2 homologue from the venom of the snake Bothrops asper: evidence of rapid plasma membrane damage and a dual role for extracellular calcium. Toxicol in Vitro 21:1382–1389. https://doi.org/10.1016/j.tiv.2007.04.010
Ward RJ, Chioato L, de Oliveira AH, Ruller R, Sa JM (2002) Active-site mutagenesis of a Lys49-phospholipase A2: biological and membrane-disrupting activities in the absence of catalysis. Biochem J 362:89–96. https://doi.org/10.1042/0264-6021:3620089
Warrell DA (2010) Snake bite. Lancet 375:77–88. https://doi.org/10.1016/S0140-6736(09)61754-2
Acknowledgements
BL and JMG thank Vicerrectoría de Investigación, Universidad de Costa Rica. AJLD thanks Sonja López for helpful feedback and support.
Funding
None.
Author information
Authors and Affiliations
Contributions
All authors contributed to writing and editing the manuscript.
Corresponding author
Ethics declarations
Conflict of interest
Authors declare no conflicts of interest.
Ethical approval
This work does not involve animals or human subjects. Ethical approval is not applicable.
Consent to participate
Not applicable.
Consent for publication
Not applicable.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
López-Dávila, A.J., Lomonte, B. & Gutiérrez, J.M. Alterations of the skeletal muscle contractile apparatus in necrosis induced by myotoxic snake venom phospholipases A2: a mini-review. J Muscle Res Cell Motil 45, 69–77 (2024). https://doi.org/10.1007/s10974-023-09662-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10974-023-09662-4