Metamorphosis of identified neurons innervating thoracic neurohemal organs in the blowfly: transformation of cholecystokininlike immunoreactive neurons.

With antisera to gastrin/cholecystokinin, we studied the postembryonic development of neurons in the thoracic ganglia of the blowfly Calliphora erythrocephala. There are some changes in the population of thoracico-abdominal neurons displaying gastrin/CCK-like immunoreactivity (CCKLI): some CCKLI neurons cannot be found after pupariation; other neurons become immunoreactive during metamorphosis. Six large thoracic CCKLI neurons could, however, be followed through metamorphosis. These CCKLI neurons innervate neuropil in thoracic ganglia and segmental neurohemal organs in the larva. In the adult insect the same neurons innervate many regions of thoracic neuropil and extensive neurohemal areas dorsally in the fused thoracico-abdominal ganglia. The immunoreactive terminals are located in the neural sheath, and electron microscopy shows that only an extracellular basal lamina separates them from the circulating hemolymph. On the basis of the location of their terminals, it can be suggested that the six CCKLI neurons have functions as neurosecretory cells both in the larva and in the adult. In both developmental stages the neurons can interact with large portions of the thoracic nervous system and release bioactive substance into the circulation. A CCK-like substance may be used both as a transmitter/neuromodulator and as a neurohormone by the same neuron. The larval neurohemal organs are described here for the first time. They show characteristics of thoracic perisympathetic organs known to exist in more primitive insects. The adult neurohemal regions on the other hand are typical of higher insects. Since the neurohemal areas are continuously (during development) innervated by the six large CCKLI neurons, we conclude that the larval neurohemal organs metamorphose into the adult neurohemal area in the neural sheath.

Peptidergic innervation of caudal neurosecretory neurons.

Luteinizing hormone releasing hormone (LHRH)-like immunoreactivity was observed in neurosecretory neurons at mesencephalic levels of the poecilid brain. This nucleus of peptide producing neurons has been shown to project to the spinal cord neurosecretory complex in this species. LHRH-like immunoreactivity was localized in fibers and terminals surrounding caudal neurosecretory cells. This investigation suggests that there is a mesencephalic descending LHRH innervation of caudal neurosecretory neurons.

In vivo application of HRP crystals: a new and efficient method for tracing neural connections in insects.

Solid HRP pellets prepared with a 2.5% Triton X-100 aqueous solution were implanted either into corpora allata or applied onto neurohemal organs of a cricket. The method presents two advantages: it allows one to perform "in vivo" instead of "in vitro" experiments, and detergent HRP pellets are easy to manipulate. Thus, this method combines simplicity with accuracy and appears to be very useful in tracing neural connections in the insect nervous system.

Neuronal and non-neuronal control of the neurosecretory caudo-dorsal cells of the freshwater snail Lymnaea stagnalis (L.).

The cerebral ganglia of the freshwater snail Lymnaea stagnalis contain two clusters of neurosecretory Caudo-Dorsal Cells (CDC). These cells produce a neurohormone which stimulates ovulation. Ganglion transplantation and quantitative electron microscopy show that neuronal isolation of the cerebral ganglia complex (CCC) results in an activation of the CDC. It was, therefore, concluded that the CDC are controlled by an inhibitory neuronal input originating outside the cerebral ganglia. Ultrastructural studies on synaptic degeneration in the CCC suggest that this input reaches the CDC via a special type of synapse-like structure, the type C-SLS. Furthermore, transplantation of CCC into acceptor snails leads to a reduced release and an increased intracellular brekdown of neurohormone in the CDC of the nervous system of the acceptors. It is supposed that these phenomena are caused by the release of an (unknown) factor from the transplanted CCC. Special attention was given to the formation and degradation of a peculiar type of neurohormone granule, the large electron dense granule. The physiological significance of the neuronal and non-neuronal control mechanisms which regulate CDC activity is discussed.