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.
Pulsations of dorsal vessel were monitored by the noninvasive techniques of contact thermography on the dorsal cuticle and by strain gauge detection of abdominal elongation movements. Diapausing pupae exhibited periods of forward-oriented, or anterograde pulsations (average duration of each pulsation 5-8 min, frequency of individual systolic strokes 10-15 per min) alternating with somewhat slower, backward-oriented or retrograde cardiac pulsations (average duration of each pulsation 6-10 min, frequency of systolic strokes 7-12 per min). The highest rate of hemolymph flow was associated with the anterograde pulsations. We studied cardiac functions in diapausing pupae because of the almost complete absence of extracardiac hemocoelic pulsations, which are much stronger and could interfere with the recordings of heartbeat in all other developing stages. The movement of abdomen associated with the heartbeat was extremely small, only some 0.14 to 0.9 µm (i.e. from one 428000th to one 66000th of the body length) and thus was not practical for routine recordings of heartbeat.
Simultaneous recordings from multiple thermographic sensors revealed the complete absence of retrograde cardiac pulsations in the head region. There are some indications that the retrograde pulsations were also lacking in the thoracic region of the aorta. The retrograde peristalsis appeared to be used for circulatory functions in the abdomen alone. By contrast, the anterograde cardiac pulsations underwent a profound amplification in the anterior part of the abdomen, entering thoracic aorta with considerable strength before reaching the final destination in the head region. The amplification of anterograde peristalsis was manifested by enhanced hemolymph flow towards the head associated with a two-fold increase in frequency of anterograde heartbeat before reaching the head region. The sensors distributed along the dorsal vessel revealed that the rate of the backward-oriented, retrograde cardiac flow of the hemolymph was also location specific. The rate of flow was lowest at the front of the abdomen, medium in the middle and highest close to the end of the abdomen. The finding of lowest hemolymph circulation at the beginning of the cardiac peristaltic waves suggested that the physiological "raison d' être" for heartbeat reversal was a need for differential enhancement of hemolymph flow towards the extremities of the immobile pupal body. The switchovers from the retrograde to anterograde cardiac pulsations were usually immediate, while the reciprocal, antero- to retro-switchovers were mostly associated with a brief cardiac arrest. Increasing temperature gradients (in 5°C steps) progressively diminished duration of both reciprocal heartbeat periods. The amplitudes of the cardiac systolic strokes also decreased with increasing temperature while the frequencies were substantially elevated.
Heartbeat reversal patterns have been monitored in the body of diapausing pupae of M. sexta 2 h before and 3 h after the injections of [Arg7]-corazonin, using noninvasive thermographic and optocardiographic methods. Large dosages (10-6 M final concentrations of corazonin in the body) caused almost immediate, adrenaline-like enhancement of the anterograde heartbeat. During the relatively short, acute phase of the tachycardia induced by corazonin, the systolic anterograde contractions of the heart increased in average from 10.5 to 24 pulses per min, culminating at 2.5 min after the injections. Duration of the acute period of tachycardia was only 7 to 20 min, which was followed by a period of slightly elevated, residual anterograde heartbeat which persisted occasionally for 1 to 3 h. Smaller dosages of corazonin (10-7M concentrations in the body) occasionally also produced a less intensive cardiotropic effect, while the more diluted samples were completely inactive. In pupae of the beetle T. molitor, injections of corazonin (10-6 M in the body) had no effect on the rate of in vivo heartbeat at all. Pharmacological analysis of the effects of corazonin in M. sexta indicated that the cardiostimulating effects of corazonin did not conform with the expected action of a peptidic neurohormone. A possibility that these effects might be artifacts produced by the low molecular breakdown products of corazonin has been discussed.