Innervation of heart and alary muscles in Sphinx ligustri L. (Lepidoptera)

Summary The origin and orientation of the heart nerves in Sphinx ligustri and Ephestia kuehniella were investigated by scanning electron microscopy using a special technique which involved pinning the dissected specimens on a stabilizing metal pad. The heart and alary muscles in Sphinx particularly their caudal extremity were also examined by transmission electron microscopy. The alary muscles form an incomplete sheath around the heart with a mainly longitudinal fibre orientation, e.i. antagonistically to the fibres of the heart itself. The heart and alary muscles are multiterminally innervated by branches of the transverse segmental nerves. All branches contain a single electron lucent axon; the thickest branches also possess several neurosecretory axons. Swellings of the segmental nerves may indicate the position of nerve cell bodies. There are no lateral heart nerves. Only one type of neuromuscular junction is abundant in the alary muscles but less frequently found in the heart. The terminals originate from the central axon only. They are capped by glial cells, which interdigitate with the muscle cells. They penetrate into the T-system toward the Z-discs and form a complex intercellular space system. Exocytosis of dense-cored vesicles into this perisynaptic reticulum seems likely. Sites of neurohaemal release are distributed along the nerve branches and special nerve endings occur at the level of the ostia. The possible nervous influence upon heart activity is discussed.The transmission electron microscopic part of this investigation was supported by a research scholarship from the Deutsche Forschungsgemeinschaft     

The ultrastructure of the Aedes aegypti heart

Comparative structural analyses of the heart and associated tissues in 4th instar larvae (L4), pupae and adults of Aedes aegypti were undertaken using a combination of microscopy techniques. The Ae. aegypti heart consists of cardiomyocytes arranged in a helical fashion, and it is physically associated with intersegmental groups of pericardial cells (PCs) and the alary muscles (AMs). Ramifications commonly present in AMs are more developed in adults than in the immature stages. Pericardial cells absorb and store extracellular components as shown by the uptake of carmine dye fed in larval diet. We also observed that carmine stained inclusions corresponding to electron-dense structures resembling lysosomes that were more abundant and prominent in pupae, suggestive of increase of waste accumulation during pupation. The results presented here expand on previously known aspects of the mosquito heart and describe for the first time comparative aspects of the morphology of the heart in different developmental stages.     

Morphology of the dorsal vessel in the abdomen of the blood-feeding insect Rhodnius prolixus

The dorsal vessel (DV) in the abdomen of the blood-feeding insect Rhodnius prolixus was divided functionally into two regions, the heart, into which haemolymph entered the DV through four pairs of ostia located in abdominal segment VII, and the aorta, along which the haemolymph was propelled from abdominal segment VI to the thorax. Osmium-fixed whole mounts revealed the DV to consist of spirally arranged striated muscle fibers and to possess two rows of ventrally attached longitudinal fibers extending the length of the abdomen. Seven pairs of alary muscles were found attached to the DV in the posterior abdominal segments. Contractions of the alary muscles attached to the ventral surface of abdominal segments VII and VIII served to expand the heart. Electron microscopy revealed the DV to consist of a thin layer of contractile elements surrounded by an inner (intima) and outer (adventitia) connective tissue layer. Embedded in the intima along each lateral side of the DV were two large groups of endocardial cells extending the length of the DV. A small group of pericardial cells was embedded in the adventitia along the mid-ventral side of the DV, and clusters of pericardial cells were found attached to the alary muscles. Nerve terminals were found only on the heart: they contained agranular synaptic vesicles approximately 30 nm in diameter and densely stained granules approximately 100-120 nm in diameter. These structural components are discussed in relation to the role of the DV in circulation.     

Peptidergic control of the heart of the stick insect, Baculum extradentatum

The dorsal vessel of the Vietnamese stick insect, Baculum extradentatum, consists of a tubular heart and an aorta that extends anteriorly into the head. Alary muscles, associated with the heart, are anchored to the body wall with attachments to the dorsal diaphragm. Alary muscle contraction draws haemolymph into the heart through incurrent ostia. Excurrent ostia lie on the dorsal vessel in the last thoracic and in each of the first two abdominal segments. Muscle fibers are associated with these excurrent ostia. Crustacean cardioactive peptide (CCAP)- and proctolin-like immunoreactivity is present in axons of the segmental nerves that project to the dorsal vessel, and in processes extending over the heart and alary muscles. Proctolin-like immunoreactive processes are also localized to the valves of the incurrent ostia and to the excurrent ostia. Neither the link nerve neurons, nor the lateral cardiac neurons, stain positively for these peptides. Physiological assays reveal dose-dependent increases in heart beat frequency in response to CCAP and proctolin. Isolating the dorsal vessel from the ventral nerve cord led to a change in the pattern of heart contractions, from a tonic, stable heart beat, to one which was phasic. The tonic nature was restored by the application of CCAP.     

Ultrastructure of the muscles of the dorsal diaphragm in Locusta migratoria

Summary The alary muscles of Locusta migratoria adults make up the major tissue of the dorsal diaphragm which separates pericardial and perivisceral sinuses in the abdomen. The alary muscles are striated with a sarcomere at rest measuring about 9 m. The Z-line has a staggered-beaded arrangement with A-bands and I-bands readily discernable. Thick myofilaments are surrounded by 10 or more thin filaments. The sarcoplasm has few mitochondria near the area of the Z-line, dyads are present and sarcoplasmic reticulum is poorly developed. Axons which innervate the alary muscle are either contained within invaginated folds of the sarcolemma of the muscle cells or the muscle cells send finger-like projections to envelop the axons. The synaptic terminals contain synaptic vesicles between 40 and 45 nm in diameter and a few electron-dense granules near or less than 170 nm in diameter. Away from synaptic terminals the axon profiles show few or no granules. The axons are accompanied everywhere by well-developed glial cells. This then is not typical neurosecretomotor innervation, however, the presence of electron-dense granules suggests the possibility of peptidergic neurotransmission.     

Immunocytochemical electron microscopic study and Western blot analysis of paramyosin in different invertebrate muscle cell types of the fruit flyDrosophila melanogaster, the earthwormEisenia foetida, and the snailHelix aspersa

Summary The presence and distribution pattern of paramyosin have been examined in different invertebrate muscle cell types by means of Western blot analysis and electron microscopy immunogold labelling. the muscles studied were: transversely striated muscle with continuous Z lines (flight muscle fromDrosophila melanogaster), transversely striated muscle with discontinuous Z lines (heart muscle from the snailHelix aspersa), obliquely striated body wall muscle from the earthwormEisenia foetida, and smooth muscles (retractor muscle from the snail and pseudoheart outer muscular layer from the earthworm). Paramyosin-like immunoreactivity was localized in thick filaments of all muscles studied. Immunogold particle density was similar along the whole thick filament length in insect flight muscle but it predominated in filament tips of fusiform thick filaments in both snail heart and earthworm body wall musculature when these filaments were observed in longitudinal sections. In obliquely sectioned thick filaments, immunolabelling was more abundant at the sites where filaments disappeared from the section. These results agree with the notion that paramyosin extended along the whole filament length, but that it can only be immunolabelled when it is not covered by myosin. In all muscles examined, immunolabelling density was lower in cross-sectioned myofilaments than in longitudinally sectioned myofilaments. This suggests that paramyosin does not form a continuous filament. The results of a semiquantitative analysis of paramyosin-like immunoreactivity indicated that it was more abundant in striated than in smooth muscles, and that, within striated muscles, transversely striated muscles contain more paramyosin than obliquely striated muscles.     

Immunochemical analysis of myosin heavy chains in the developing chicken heart

Monoclonal antibodies (McAb) against myosin from the pectoralis muscle of the adult chicken have been generated and shown to react specifically with the myosin heavy chain (MHC). The reactivities of two such McAbs with myosin from adult chicken atrial and ventricular myocardium were further analysed by immunoautoradiography, radioimmunoassay, and immunofluorescence microscopy. Monoclonal antibody MF 20 was found to bind both atrial and ventricular MHC and stain all striated muscle cells of the adult chicken heart. In contrast, McAb B1 bound specifically to atrial myocytes in immunofluorescence studies, while immunoautoradiography and radioimmunoassay demonstrated the specificity of this antibody for the atrial MHC. Upon reacting these McAbs with myosin isolated from embryonic hearts where definitive atria and ventricles were present, the same specificity of antibody binding was observed. Immunofluorescence studies demonstrated that all striated muscle cells of the embryonic heart contained MHCs recognized by MF 20, while only atrial muscle cells were bound by B1. When extracts of presumptive atrial and ventricular tissue were reacted with MF 20 and B1, significant reactivity of MF 20 was first observed at stage 10 in the presumptive ventricle and thereafter this McAb reacted with all regions of the developing myocardium. Binding of B1 was detected approximately 1 day later at stage 15 and was confined to atrial-forming tissues. These data demonstrate antigenic similarity between adult and embryonic MHC isolated from atrial myocardium and suggest the expression of an atrial-specific MHC early in the regional differentiation of the heart.     

Characterization of a myosin heavy chain in the conductive system of the adult and developing chicken heart

A monoclonal antibody (anterior latissimus dorsi 58 [ALD58]; antimyosin heavy chain, MHC) directed against myosin from slow tonic muscle was found to react specifically with the striated muscle cells of the conductive system in the adult chicken heart. This monoclonal antibody was used to study the expression of myosin in the conductive system of the adult and developing heart. Using immunofluorescence microscopy with ALD58, muscle cells of the conductive system were demonstrated in both the atria and ventricles of the adult heart as previously shown by Sartore et al. (Sartore, S., S. Pierobon-Bormioli, and S. Schiafinno, 1978, Nature (Lond.), 274: 82-83). Radioactive myosin from adult atria and ventricles was precipitated with ALD58 and subjected to limited proteolysis and subsequent peptide mapping. Peptide maps of ALD58 reactive myosin from atria and ventricles were very similar, if not identical, but differed from peptide maps of ordinary atrial and ventricular myosin. The same antibody was used to study cardiac myogenesis in the chick embryo. When ALD58 was reacted with myosin isolated from atria and ventricles at selected stages of development in radioimmunoassays, reactivity was not observed until the last week of embryonic life (greater than 15 d of egg incubation). Thereafter concomitant and progressively increased reactivity was observed in atrial and ventricular preparations. Also, no ALD58 positive cells were observed in immunofluorescence studies of embryonic hearts until 17 d of egg incubation. Primary cell cultures of embryonic hearts also proved to be negative for this antibody. This study demonstrates that an epitope recognized by ALD58 associated with an antimyosin heavy chain of striated muscle cells of the adult heart conductive system is absent or present in only small amounts in the early embryonic heart.     

Microanatomy of the heart and associated structures of two scorpions,Centruroides sculpturatus ewing and Uroctonus mordax thorell

Spiroid orientation of the circumferential heart wall muscles is described for Centruroides sculpturatus Ewing. This muscle arrangement accounts for differences in ostial position when the heart of this species is compared to that of Uroctonus mordax Thorell. Other differences, such as number of lateral arteries present, cannot be explained on the basis of circumferential muscle orientation. The histology of the heart and associated vessels, but not the supraneural vessel, was found to be similar in both species. The lateral, posterior, communicating and sternal arteries all possess a muscularis composed of irregularly spaced, apparently branched, striated muscle fibers. External to this is a covering of connective tissue. The lumina of these arteries, the aorta, and the supraneural vessel are lined with a homogeneous, PAS-positive membrane. This membrane is also seen in blood vessels which penetrate the nervous system. It was not observed in vessels accompanying major nerves. Findings are compared to those of other authors. Differences in the structure of the hearts of these two species are discussed in relation to the microanatomy of other arachnid hearts.     

Control of the alary muscles of locust dorsal diaphragm

ABSTRACT. The heartbeat in whole, intact, adult Locusta migratoria R.F. was characterized by a regular rate but apparently irregular amplitude. Cutting segmental nerves often eliminated apparent amplitude fluctuations, and electrically shocking a segmental nerve in the whole animal evoked apparent amplitude changes corresponding to the shocks. Saline-perfused tissue preparations showed that the apparent amplitude fluctuations could be duplicated by segmental nerve stimulation, and that the fluctuations were due largely to contractions of the alary muscles of the dorsal diaphragm which shifted the position of the heart chamber without a change in volume. The alary muscles are each multi-terminally innervated by one motor axon. Neurally-evoked postsynaptic potentials facilitated and summated, and the diaphragm muscles began visibly contracting at stimulation rates as low as 2 Hz. Stimulation at higher frequencies caused greater depolarization of the muscle fibres with no indication of electrically-excited responses. The alary muscles were insensitive to perfusion with acetylcholine, l -glutamate, l -aspartate, dopamine, octopamine, noradrenaline, proctolin, 5-hydroxytryptamine, or gamma aminobutyric-acid in saline at concentrations up to 10^-3M. Larval or adult brain extracts of Locusta at 10 μg/μl and diluted 1:5 in saline caused uniform contractions of the alary muscle preparation, while perfusion of skeletal muscle extracts produced no response.     

Reproductive performance of <Emphasis Type="Italic">Nesolynx thymus</Emphasis> (Hymenoptera: Eulophidae) as influenced by host (<Emphasis Type="Italic">Musca domestica</Emphasis>) size

An investigation was conducted to understand the influence of host size on the reproductive performance of Nesolynx thymus, an ecto-pupal parasitoid of the uzi fly, Exorista bombycis, inflicting 10–20% loss to silkworm crops in the southern silk producing states of India. Two day-old adults of N. thymus were allowed to parasitize pupae of M. domestica, categorized into big and small at a parasitoid-host ratio of 1:20. After parasitoid adult eclosion, data on parasitization rate, developmental duration, male, female and total adult recovery per pupa and per female, sex ratio, adult size and adult longevity were recorded. The performance of first generation adults as influenced by host size was also recorded by allowing the first generation adults to parasitize three day-old pupae of E. bombycis. The parameters female and total progeny production per female, sex ratio, longevity, body length and wing span of males, females, head width of male, and abdomen length of female increased significantly with host size. No impact of host size was observed on performance of first generation adults.     

Fine structure of the alary muscles of the American cockroach

The alary muscles of the cockroach, Periplaneta americana, are striated with an A-band of 3·0 to 3·5 μm long. Each muscle fibre was 10 to 12 μm in diameter and Z-lines appeared as small discrete units staggered throughout the sarcoplasm. Mitochondria were conspicuously located near the Z-line areas and were absent from the middle portion of the sarcomere. A transverse membrane system was present which formed dyad structures with a relatively sparse sarcoplasmic reticulum. Cockroach alary muscles were innervated by axons containing electron-dense granules of near 100 nm in diameter. These are thought to be typical of ‘neurosecretory’ axons based on their ultrastructural appearance.     

Dietary Conjugated Linoleic acid (CLA) in House Fly,Musca domestica,with no Adverse Effects on Development

Conjugated linoleic acid (CLA) acts as a potent cancer inhibitor and biological modulator in several animal models by incorporation in the lipid fractions. Now we report the possibility of incorporation of dietary CLA into insect body lipids. Chemically-synthesized CLA from safflower seed oil was supplied to house fly (Musca domestica) larvae and adults with diet supplements at various levels. Amount of CLA in the pupa and adult body was proportional to the concentrations of CLA in the diet. CLA amount in pupae and adults was 0.17 mg/g and 0.41 mg/g of body, respectively, by 0.1% CLA diet (the lowest dosage), whereas it dramatically increased to 3.05 mg/g and 1.51 mg/g of body, respectively, by 10% CLA diet (the highest dosage). The dietary CLA did not show any adverse effects on the development of larvae and pupae, survivorship and fertility of adults, and eclosion of deposited eggs.     

Label‐free imaging of redox status and collagen deposition showing metabolic differences in the heart

The heart has high metabolic demand to maintain function. The primary source of energy supply to support correct contractile muscle function differs between a fetus and an adult. In fetal life, ATP is primarily generated by glycolysis and lactate oxidation, whereas following birth, there is a shift towards a reliance on mitochondrial metabolism and fatty acid oxidation. This change in metabolic status is an adaptation to different fuel availability, oxygenation and growth patterns. In this study, we have employed 2‐photon excitation fluorescence microscopy to define the relationship between two critical metabolic cofactors nicotinamide adenine dinucleotide(P)H and flavin adenine dinucleotide, effectively utilizing a redox ratio to differentiate between the metabolic status in fetal (proliferative) and adult (quiescent/hypertrophic) hearts. Two‐photon imaging was also used to visually confirm the known increase in collagen deposition in the adult heart. The changes observed were consistent with a hypertrophic growth profile and greater availability of fatty acids in the adult heart, compared to the proliferative fetal heart. Two‐photon excitation fluorescence microscopy is therefore a convenient imaging technology that enables the monitoring of striated muscle architecture and the metabolic status of heart tissue. This imaging technology can potentially be employed to visualize cardiac and other muscle pathologies.      

Development of the larval muscle system in the mussel Mytilus trossulus (Mollusca,Bivalvia)

In the present study we examined muscle development throughout the complete larval cycle of the bivalve mollusc, Mytilus trossulus. An immunofluorescence technique and laser scanning confocal microscopy were used in order to study the organization of the muscle proteins (myosin, paramyosin, twitchin, and actin) and some neurotransmitters. The appearance of the muscle bundles lagged behind their nervous supply: the neuronal elements developed slightly earlier (by 2 h) than the muscle cells. The pioneer muscle cells forming a prototroch muscle ring were observed in a completed trochophore. We documented a well‐organized muscle system that consisted of the muscle ring transforming into three pairs of velar striated retractors in the early veliger. The striations were positive for all muscle proteins tested. Distribution of FMRFamide and serotonin (5‐HT) immunocytochemical staining relative to the muscle ring differed significantly: 5‐HT‐immunioreactive cells were situated in the center of the striated muscle ring, while Phe‐Met‐Arg‐Phe‐NH2 neuropeptide FMRFamid immunoreactive fibers were located in a distal part of this ring. Our data showed clearly that the muscle proteins and the neurotransmitters were co‐expressed in a coordinated fashion in a continuum during the early stages of the mussel development. Our study provides the first strong evidence that mussel larval metamorphosis is accompanied by a massive reorganization of striated muscles, followed by the development of smooth muscles capable of catch‐contraction.     

Heart structure and beat in the stable fly, Stomoxys calcitrans

ABSTRACT. The heart of the adult stable fly, Stomoxys calcitrans (L.), is suspended from the dorsal sclerites of the abdomen by strands of connective tissue, and supported from below by alary muscles that insert into a central band of longitudinal muscle just beneath the aorta. Valved openings occur in three of the heart segments. The central band of muscle beneath the heart is innervated but there is no well-defined lateral cardiac nervous system. The myocardium consists of a single layer of circular muscle composed of a series of muscle fibres that are joined dorsally and ventrally by intercalated discs in the midline of the insect. T-system tubules are closely associated with the sarcoplasmic reticulum, forming dyads. The heart rate of intact stable flies varied from short intervals of almost no activity to periods with a very rapid beat (126–294 pulses/min), and when the connections to the central nervous system were severed the heart beat became very regular (258 pulses/min). Slight pressure applied to the dorsal septum stopped myocardial contractions in that segment. The myocardium was insensitive to perfusion with 10^-3M acetylcholine, l -aspartic acid, l -glutamic acid, Λ-aminobutyric acid, 5-hydroxytryptamine, octopamine, tyramine and proctolin 10^-5 m. However, Mn⁺⁺ caused either an intermittent beat at lower concentrations (0.5 min) or near arrest at higher concentrations (2 mM).     

Fluorescent Labeling of Drosophila Heart Structures

The Drosophila melanogaster dorsal vessel, or heart, is a tubular structure comprised of a single layer of contractile cardiomyocytes, pericardial cells that align along each side of the heart wall, supportive alary muscles and, in adults, a layer of ventral longitudinal muscle cells. The contractile fibers house conserved constituents of the muscle cytoarchitecture including densely packed bundles of myofibrils and cytoskeletal/submembranous protein complexes, which interact with homologous components of the extracellular matrix. Here we describe a protocol for the fixation and the fluorescent labeling of particular myocardial elements from the hearts of dissected larvae and semi-intact adult Drosophila. Specifically, we demonstrate the labeling of sarcomeric F-actin and of α-actinin in larval hearts. Additionally, we perform labeling of F-actin and α-actinin in myosin-GFP expressing adult flies and of α-actinin and pericardin, a type IV extracellular matrix collagen, in wild type adult hearts. Particular attention is given to a mounting strategy for semi-intact adult hearts that minimizes handling and optimizes the opportunity for maintaining the integrity of the cardiac tubes and the associated tissues. These preparations are suitable for imaging via fluorescent and confocal microscopy. Overall, this procedure allows for careful and detailed analysis of the structural characteristics of the heart from a powerful genetically tractable model system.Download video file.^{(130M, mp4)}     

Functional morphology of the dorsal vessel in the adult fly Protophormia terraenovae (diptera,calliphoridae)

The morphology and ultrastructure of the contractile tubular vessel acting as the cardiac pump in Protophormia terraenovae flies were analyzed by means of light microscopy, SEM and TEM. The results provide a novel anatomical picture of the two vessel portions, the abdominal heart and the aorta, and lay the foundations for an interpretation of the cardiocirculatory function in the fly. In the thorax, the thin and unchambered aorta is without apertures, while the abdominal heart presents a very small caudal aperture and pairs of lateral ostia, one in each of the five chambers of which it is composed. The ostia of the four more distal chambers are of the incurrent type, which is to say that they act as valves ensuring that hemolymph flows only into the heart. Conversely, the ostia in the most proximal chamber allow hemolymph to flow both into and out of the heart. The entire vessel is composed of a single layer of myofibers that are oriented circularly around the lumen in the abdominal heart and longitudinally in the thoracic aorta. The abdominal heart has a thicker wall, a far more diffused and thick distribution of tracheoles, and a far greater number of mitochondria with respect to the aorta. This arrangement ensures a greater availability of oxygen and energy in the abdominal heart compared to the aorta and leads one to suppose that the high‐ and low‐frequency contractions of the cardiac cycle (Thon, [1982] J. Insect Physiol. 28:411–416) can be attributed to the abdominal heart and the aorta, respectively. J. Morphol. 240:15–31, 1999. © 1999 Wiley‐Liss, Inc.     

Molecular and functional characterization of the flightin gene in the Oriental fruit fly,Bactrocera dorsalis

Flightin is a protein in flight muscles and is crucial for the flight capacity. Flightin also has been proposed as a protein with deep ancestry and functions outside of flight muscles. However, functional and molecular characterization of flightin achieved so far is mainly in flight muscles of Drosophila. Here, we cloned the flightin (Bd-flightin) gene and tested its expression and function in Bactrocera dorsalis, an important migratory pest. Phylogenetic analysis based on flightin orthologs revealed that the divergence of flightin is consistent with the taxonomic classification of insects. Motif analysis indicated obvious variations in flightin orthologs, which may have occurred during speciation and functional differentiation. The expression is quite low during egg and larval stages, which largely increased during pupal stage and then peaked at the beginning of the adult stage. Bd-flightin also showed tissue- and age-specific expression patterns during adult stage. The relative expression level is low in wing, head, ovary and testis, which is relatively higher in leg and abdominal wall and much higher in thorax. Injection of late pupae and newly eclosed adults with 1 μg flightin dsRNA per insect both significantly reduced the expression of flightin and the flight capacity in males and females. In addition, silencing the expression of flightin also decreased the weight ratio of thorax and whole-body. These results suggested that flightin plays important roles in flight muscle development and flight function in B. dorsalis, which can potentially be used to control the flight behaviour of the fruit fly.