Pupal Heart Research Articles

Structure-activity relationship data and ligand-receptor interactions identify novel agonists consistent with sulfakinin tissue-specific signaling in Drosophila melanogaster heart.

The structures and activities of invertebrate sulfakinins that influence gut motility and heart rate are like the vertebrate cholecystokinin (CCK) peptides. Typical of sulfakinin precursors Drosophila melanogaster encodes non-sulfated drosulfakinin I (nsDSK I; FDDYGHMRF-NH2) and nsDSK II (GGDDQFDDYGHMRF-NH2) that bind DSK-R1 and DSK-R2. To explore the role of the nsDSK II N-terminal extension (GGDDQ) in gut we delineated its structure-activity relationship (SAR) and identified novel agonists. We then predicted the nsDSK II extension SAR is tissue specific consistent with cardiac CCK structure activity and signaling being different from gut. To evaluate our hypothesis, we tested single-substituted alanine and asparagine analogs in heart. We found alanyl-substituted analogs were less active in heart than nsDSK II; in gut they include a super agonist and a protean agonist. Additionally, we discovered ns[N4]DSK II was more active than nsDSK II in pupal heart, while ns[N3]DSK II was inactive. In contrast, ns[N3]DSK II and ns[N4]DSK II were super agonists in adult heart, yet inactive in larva. Although we reported nsDSK II acts through DSK-R2 in gut, its identity in heart was unknown. Here we reviewed ligand-receptor interactions in conjunction with SAR data to suggest nsDSK II acts through DSK-R1 in heart consistent with sulfakinin tissue-specific signaling.

Structure–activity and immunochemical data provide evidence of developmental- and tissue-specific myosuppressin signaling

Myosuppressin peptides dramatically diminish contractions of the gut and heart. Thus, delineating mechanisms involved in myosuppressin signaling may provide insight into peptidergic control of muscle contractility. Drosophila myosuppressin (DMS, TDVDHVFLRFamide) structure–activity relationship (SAR) was investigated to identify an antagonist and explore signaling. Alanyl-substituted, N-terminal truncated, and modified amino acid analogs identified residues and peptide length required for activity. Immunochemistry independently provided insight into myosuppressin mechanisms. DMS decreased gut motility and cardiac contractility dose dependently; the different effective concentrations at half maximal-response were indicative of tissue-specific mechanisms. Replacement of aspartic acid 2 (D2) generated an analog with different developmental- and tissue-specific effects; [A2] DMS mimicked DMS in adult gut (100% inhibition), yet decreased larval gut contractions by only 32% with increased potency in pupal heart (126% inhibition). The DMS active core differed across development and in tissues; adult (DHVFLRFamide) and larval gut (TDVDHVFLRFamide), and adult (VFLRFamide) and pupal heart (VFLRFamide). Substitution of D2 and D4 with a modified amino acid, p-benzoyl-phenylalanine, produced developmental- and tissue-specific antagonists. In the presence of protease inhibitors, DMS and VFLRFamide were more effective in adult gut, but lower or unchanged in pupal heart compared to peptide or analog alone, respectively. DMS-specific antisera stained neurons that innervated the gut or heart. This study describes novel antagonists and data to identify developmental- and tissue-specific mechanisms underlying the pleotropic effects of myosuppressin in muscle physiology.

Heartbeat reversal after sectioning the dorsal vessel and removal of the brain of diapausing pupae of Manduca sexta (Lepidoptera: Sphingidae)

Reversal of heartbeat was monitored in vivo by noninvasive, multisensor, thermo-cardiographic and pulse-light, opto-cardiographic techniques. The dorsal vessel was sectioned at the beginning, in the middle and near the end of the abdomen. Changes in the heartbeat were simultaneously monitored in both the disconnected anterior and posterior sections of the heart. The results revealed the existence of a caudal regulatory cardiac centre located in the fused A7-A10 abdominal segments. Posterior sections, containing this terminal ampulla of the heart always exhibited a more or less normal heartbeat reversal, including both anterograde and retrograde pulsations. This shows that the forward-oriented as well as the reciprocal, backward-oriented peristaltic waves of the heart are both regulated from the posterior regulatory center, without involvement of the cephalic region. The cardiac pulsations in the anterior sections of the heart were paralysed and seriously impaired by the lesions. During the acute phase after the lesions, anterior sections showed only some convulsion-like, unidirectional, backward-oriented peristaltic pulsations of low frequency. Within one or two days after the lesions, isolated anterior sections of the heart developed a subsidiary heartbeat regulation associated with the oscillating, bi-directional peristaltic waves running alternatively, forward and backward in opposite directions. After a few days, the previously paralysed anterior sections of the heart were able to develop perfectly coordinated patterns of heartbeat reversal. At this time, the two asynchronous heartbeat patterns ran separately in each of the divided sections of the heart. One or two weeks later, reversal of the heartbeat occasionally occurred synchronously along the entire length of the dorsal vessel. Sectioning of the ventral nerve cord, removal of the cephalic nervous system (brain, frontal ganglion, suboesophageal ganglion and the associated nerves) or removal of the fused terminal abdominal ganglionic mass and adjacent caudal nerves, had no effect on the pattern of heartbeat reversal. These facts indicate that the pupal heart of M. sexta operates purely myogenically, like the human heart. The myogenic pacemakers of the caudal regulatory cardiac centre (analogous to the atrio-ventricular nodes of the human heart) are autonomous, generating inherent rhythmicity without intervention from the nervous system. Development of subsidiary pacemakers regulating rhythmicity in the lesioned myocardium and restitution of the synchronized contracting integrity between the two disconnected sections of the heart are new cardiological features, which merit further investigation.

Effects of population structure and sex on association between serotonin receptors and Drosophila heart rate.

As a first step toward population and quantitative genetic analysis of neurotransmitter receptors in Drosophila melanogaster, we describe the parameters of nucleotide variation in three serotonin receptors and their association with pupal heart rate. Thirteen kilobases of DNA including the complete coding regions of 5-HT1A, 5-HT1B, and 5-HT2 were sequenced in 216 highly inbred lines extracted from two North American populations in California and North Carolina. Nucleotide and amino acid polymorphism is in the normal range for Drosophila genes and proteins, and linkage disequilibrium decays rapidly such that haplotype blocks are typically only a few SNPs long. However, intron 1 of 5-HT1A consists of two haplotypes that are at significantly different frequencies in the two populations. Neither this region of the gene nor any of the common amino acid polymorphisms in the three loci associate with either heart rate or heart rate variability. A cluster of SNPs in intron 2 of 5-HT1A, including a triallelic site, do show a highly significant interaction between genotype, sex, and population. While it is likely that a combination of weak, complex selection pressures and population structure has helped shape variation in the serotonin receptors of Drosophila, much larger sampling strategies than are currently adopted in evolutionary genetics will be required to disentangle these effects.

Screening assays for heart function mutants in Drosophila.

The rapid life cycle and genetic tractability of Drosophila make it an ideal organism for large-scale genetic screens. Here we describe a novel assay for pupal heart rate and rhythmicity as well as techniques to measure adult cardiac stress response. These assays can be powerfully combined to concurrently screen for both mutations affecting cardiac function and mutations affecting the age-dependent decline in adult cardiac stress response. Mutations identified in such screens have the potential to contribute greatly to the understanding of both congenital heart disease and the regulation of age-dependent decline in cardiac function in the human population.

A nonpeptide provides insight into mechanisms that regulate Drosophila melanogaster heart contractions

Here we report the effect of a nonpeptide, benzethonium chloride (bztc), on Drosophila melanogaster larval, pupal, and adult heart rates in vivo. Benzethonium chloride reduced the frequency of spontaneous contractions in the D. melanogaster pupal heart, but not in the larval heart or the adult heart as measured in noninvasive whole animal preparations. When applied directly to the D. melanogaster heart, in the absence of hemolymph, bztc reduced the frequency of spontaneous contractions in larval, pupal, and adult hearts. These findings are consistent with the conclusion that bztc acts through or is regulated by different mechanisms in these three developmental stages. An alternative explanation is that larval hemolymph and adult hemolymph contain a material that interferes with the effect of the nonpeptide on heart contractions. Bztc mimicked the effect of the peptide dromyosuppressin (DMS) on the heart at an equivalent concentration; in contrast, 103-fold more nonpeptide is required to mimic the effect of DMS on fly gut. These findings are consistent with the presence of tissue-specific myosuppressin receptors or mechanisms.

Morphology of the pupal heart, adult heart, and associated tissues in the fruit fly, Drosophila melanogaster

The early pupal heart of the fruit fly Drosophila melanogaster has recently been the subject of intense physiological and molecular work, yet it has not been well described, nor has it been compared with the heart of the adult fly. In the work reported here, the hearts of adults and early pupae of D. melanogaster were studied by scanning and transmission electron microscopy and by light microscopy. The hearts of adults and early pupae both consist of a tube of circular striated muscle one cell in thickness. The alary muscles, which suspend the heart, are more delicate in the adult compared to the early pupa. The pericardial cells in both early pupae and adults are connected to the heart by connective tissue radiating from the alary muscles or dorsal diaphragm. We confirm that four major changes occur in the heart during metamorphosis: 1) a conical chamber is formed de novo in the first and second abdominal segments; 2) the adult heart curves to conform to the contour of the abdomen; 3) a layer of longitudinal striated muscle appears on the ventral surface of the heart; 4) a fourth pair of ostia is added to the three already present in the early pupa; and note additionally that 5) the ostia appear as simple openings in the heart of the early pupa but are valve-like in the adult. J. Morphol. 240:225–235, 1999. © 1999 Wiley-Liss, Inc.

Morphology of the pupal heart, adult heart, and associated tissues in the fruit fly, Drosophila melanogaster.

The early pupal heart of the fruit fly Drosophila melanogaster has recently been the subject of intense physiological and molecular work, yet it has not been well described, nor has it been compared with the heart of the adult fly. In the work reported here, the hearts of adults and early pupae of D. melanogaster were studied by scanning and transmission electron microscopy and by light microscopy. The hearts of adults and early pupae both consist of a tube of circular striated muscle one cell in thickness. The alary muscles, which suspend the heart, are more delicate in the adult compared to the early pupa. The pericardial cells in both early pupae and adults are connected to the heart by connective tissue radiating from the alary muscles or dorsal diaphragm. We confirm that four major changes occur in the heart during metamorphosis: 1) a conical chamber is formed de novo in the first and second abdominal segments; 2) the adult heart curves to conform to the contour of the abdomen; 3) a layer of longitudinal striated muscle appears on the ventral surface of the heart; 4) a fourth pair of ostia is added to the three already present in the early pupa; and note additionally that 5) the ostia appear as simple openings in the heart of the early pupa but are valve-like in the adult.

Neural transmitters and a peptide modulate Drosophila heart rate

Neural messengers affect Drosophila heart rate. Serotonin increases larval, pupal, and adult heart rate. Octopamine and dopamine are inactive in larva, decrease pupal rate, and increase adult heart rate. Acetylcholine and nicotine decrease larval and pupal heart rate, while acetylcholine decreases and nicotine increases adult heart rate. Muscarine decreases pupal heart rate, but is inactive in larva and adult. GABA is inactive in larva and adult, but decreases pupal heart rate. Glutamate is inactive in larva and pupa, but decreases adult heart rate. Proctolin decreases heart rate in all three stages. Caffeine acts only to decrease adult heart rate.

PHYSIOLOGY OF INSECT DIAPAUSE. XII. THE MECHANISM OF CARBON MONOXIDE-SENSITIVITY AND -INSENSITIVITY DURING THE PUPAL DIAPAUSE OF THE CECROPIA SILKWORM

1. The heartbeat of the adult Cecropia moth is inhibited by suitable pressures of carbon monoxide, and this inhibition is reversed by light.2. The wave-lengths which are maximally effective in reversing the CO-inhibition are in good agreement with the absorption maxima of the CO-cytochrome oxidase complex.3. Therefore, the terminal oxidase of the adult heart may be identified as cytochrome oxidase.4. The situation is much more complex in the case of the diapausing pupa. The latter shows a considerable capacity for anaerobic metabolism, and its heart can beat for several hours in the total absence of oxygen. Moreover, normal heartbeat continues indefinitely in the presence of oxygen pressures as low as 0.5% atm.5. After exhaustion of the "anaerobic reserve," the pupal heart may be said to be "micro-aerophilic." Oxygen is required but a remarkably low tension suffices.6. At ordinary oxygen pressures such as that in air, it is difficult or impossible to demonstrate any sensitivity of the pupal heart to carbon monoxide. However, when the oxygen tension is decreased to very low levels, the heartbeat shows a clear sensitivity to carbon monoxide. Thus, at the low oxygen tension of 0.18% atm., the pupal heartbeat is inhibited 50 per cent by carbon monoxide at a pressure of only 5 mm. Hg.7. Under these circumstances, the inhibition of the pupal heartbeat is light-reversible.8. The actions of oxygen and carbon monoxide are considered in detail. The terminal oxidase of the pupal heart is found to be cytochrome oxidase.9. The resistance of the pupal heart to carbon monoxide and to low oxygen pressures can be accounted for in terms of the presence in the pupal heart of a great excess of cytochrome oxidase relative to cytochrome c.

PHYSIOLOGY OF INSECT DIAPAUSE. XI. CYANIDE-SENSITIVITY OF THE HEARTBEAT OF THE CECROPIA SILKWORM, WITH SPECIAL REFERENCE TO THE ANAEROBIC CAPACITY OF THE HEART

1. During the course of metamorphosis the heart of the Cecropia silkworm appears to undergo pronounced shifts in its sensitivity to cyanide.2. In the mature larva the heartbeat is promptly blocked by 10-3 M cyanide; in the adult moth it is even more sensitive and is brought to a standstill by 10-5 M cyanide.3. In the intervening pupal stage the heart is insensitive to acute poisoning by physiological concentrations of cyanide.4. This insensitivity is observed only in experiments of short duration. When the exposure to cyanide is continued for many hours, the pupal heartbeat is blocked by 10-2 or 10-5 M cyanide.5. The paradoxical response of the pupal heart can be accounted for in terms of a pronounced capacity for anaerobic metabolism which is peculiar to this particular stage. The pupal heart can beat for as long as 5½ hours in the complete absence of oxygen. During this same period the heart is insensitive to cyanide.6. While discounting any true insensitivity of the pupal heart to cyanide, the experime...