Abstract

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.

Highlights

  • Investigations of the dorsal vessel of insects and other arthropods were common topics of many papers and review articles some three decades ago (Krijgsman, 1952; McCann, 1963; Wigglesworth, 1972; Jones, 1977; Miller, 1977, 1985, 1997; Wasserthal, 1996)

  • The possibility that an insect heart might be regulated by neurogenic factors was reopened by work on Bombyx mori (Ai & Kuwasawa, 1995)

  • The anteriorly directed contractions are usually rapid, and the posterior waves slow”. These characteristic features of the insect dorsal vessel are true for M. sexta, recorded visually and with a stopwatch a quarter of a century ago

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Summary

Introduction

Investigations of the dorsal vessel of insects and other arthropods were common topics of many papers and review articles some three decades ago (Krijgsman, 1952; McCann, 1963; Wigglesworth, 1972; Jones, 1977; Miller, 1977, 1985, 1997; Wasserthal, 1996). The possibility that an insect heart might be regulated by neurogenic factors was reopened by work on Bombyx mori (Ai & Kuwasawa, 1995) According to these authors, the pattern of heartbeat reversal is controlled by nerves from the frontal ganglion and the recurrent nervous system. Similar involvement of the nervous system in regulating the heartbeat was observed in adult Manduca sexta (Dulcis et al, 2001). In this case the regulation was traced to nerves of the fused A7–A8 terminal abdominal ganglion. One located in the frontal part of the aorta and the other within the neurons of the terminal abdominal ganglion at the opposite end of the body

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