Neurosecretory system of the earwig Labedura riparia, and the rôle of the aorta as a neurohaemal organ

The neurosecretory system of Labedura riparia has been described from sections and whole mounts using a variety of techniques. The pars intercerebralis contains two clusters of medial neurosecretory cells (MNC), each cluster consisting of 8 to 10 A-cells and occasional B-cells. The lateral sides of the brain have a few B-cells. The axons of the median neurosecretory cells terminate in the cephalic aorta (AO), whereas the axons of the lateral neurosecretory cells (LNC) terminate in the corpora cardiaca (CC). It appears that the neurosecretory material (NSM) elaborated in the MNC is stored in the cephalic aorta and that elaborated in the LNC is stored in the corpora cardiaca, which are two oval or elongate bodies composed of large chromophobe and small chromophil cells. Posteriorly there is the oval or elongate corpus allatum (CA) attached to the CC by thick nerves. The CA consists of one cell type only. Both CC and CA contain no A-cell neurosecretory material. It has been suggested that the neurosecretory system of L. riparia is composed of two complexes. One is formed by the medial neurosecretory cells for which the aorta functions as a neurohaemal organ, and the other is formed by lateral neurosecretory cells-lateral neurosecretory pathways-nervi corporis cardiaci-II in which the corpora cardiaca function as a neurohaemal organ.     

Ultrastructure of retrocerebral complex of the earwig, Euborellia annulipes, and rôle of aorta as a neurohaemal organ

The ultrastructure of the retrocerebral endocrine-aortal complex of the earwig, Euborellia annulipes has been studied. The space between the inner and outer stromal layers of the aorta is occupied by numerous axon terminals and pre-terminals containing large electron dense granules (NS-I) of approximately 100 to 220 nm and a few axon terminals having small granules (NS-II) of approximately 40 to 90 nm; the former appear to belong to medial neurosecretory A-cells, and the latter to the B-cells of the brain. The corpora cardiaca consist of intrinsic cells with mitochondria and multivesicular bodies. Granules of type NS-II and NS-III are observed in the axon terminals and pre-terminals in the corpora cardiaca. The NS-II are identical to those found in the aorta and are probably the secretions of the lateral B-cells. Granules of type NS-III are 40 to 120 nm and electron dense, and are intrinsic in origin. Similar granules occur in the intrinsic cells of the corpora cardiaca. E M studies have confirmed the rôle of the aorta as a neurohaemal organ for the medial neurosecretory cells, and the corpora cardiaca for the lateral neurosecretory cells of the brain. The corpora cardiaca also act as a reservoir for the intrinsic secretion. The corpus allatum is a solid body consisting of parenchymal cells with prominent nuclei, mitochondria, and endoplasmic reticulum. In between its cells are occasional glial cells and also neurosecretory as well as non-neurosecretory axons. The gland is devoid of A-cell NSM.     

Hormonal control of lipid synthesis in the fat body of the adult female tsetse fly, Glossina morsitans

Aqueous extracts of brain, thoracic ganglion or corpora cardiaca of female Glossina morsitans were shown to contain a substance which inhibited the synthesis of lipid from l[U-¹⁴C] leucine by fat cells incubated in vitro. The highest concentration of this substance was found in the corpora cardiaca; approximately 1 × 10^?6 gland pairs μl^?1 were required for maximum inhibition. At concentrations greater than 1 × 10^?4 gland pairs μl^?1 the lipid synthesis inhibiting factor (hereafter referred to as the LSIF) was inactivated by the presence of a substance which could be removed by gel filtration. The concentration of LSIF in the corpora cardiaca and midbrain varied throughout the reproductive cycle of the female. Net release of LSIF from the midbrain occurred between the 2nd and 7th day of the 9-day reproductive cycle. Net release from the corpora cardiaca began on day 5 and continued until the end of the interlarval period on day 9. Results are consistent with the hypothesis that LSIF is synthesised mainly in the medial neurosecretory cells of the midbrain whereas the corpora cardiaca are the site of storage and release into the haemolymph. LSIF was present in midbrain and corpora cardiaca extracts from male G. morsitans but at lower concentrations than in females. No variation in LSIF concentration could be correlated with the feeding cycle. LSIF activity was not detected in fresh haemolymph but was found at high concentration in boiled haemolymph, suggesting the presence of an inhibitor which was inactivated at high temperature. Preliminary investigations into the nature of LSIF have shown it to be inactivated by proteolytic enzymes and to be recoverable in a single peak from a Sephadex G15 column.Results support the view that LSIF is a peptide hormone which, in conjunction with an inhibitor, controls the lipid synthetic ability of the fat cells of the adult female tsetse fly throughout the reproductive cycle.     

Anatomy of the neurosecretory cells in the cerebral and subesophageal ganglia of the female European corn borer moth,Ostrinia nubilalis (Hübner) (Lepidoptera: Pyralidae)

The anatomy of the neurosecretory cells in the brain-subesophageal ganglion complex of female European corn borer moth Ostrinia nubilalis (Lepidoptera: Pyralidae) was studied using histological and cobalt backfilling techniques. Histological staining revealed the presence of 2 median and one lateral neurosecretory cell groups in the brain. These brain neurosecretory cells are made up of mainly type A cells with a few type B cells in the median group. Three type C neurosecretory cell clusters occupy the apparent mandibular, maxillary, and labial neuromeres at the ventral median aspect of the subesophageal ganglion. Axonal pathways of the neurosecretory cell groups were delineated by retrograde cobalt filling from the corpora cardiaca. Fibers of the 3 brain neurosecretory cell groups merged to form a distinct axonal tract that exits the brain via the fused nervi corporis cardiaci-1 + 2. Cobalt backfilling from the corpora cardiaca filled 4 groups of cell bodies in the subesophageal ganglion. The presence in the subesophageal ganglion of extensive dendritic arborizations derived from the brain suggests interactions between neurosecretory cell groups in the 2 head ganglia.     

Experimental evidence for a neuroendocrine control of ecdysone biosynthesis in adult females of Locusta migratoria

The considerable increase in ecdysteroid concentration which occurs in normal Locusta ovaries at the end of each cycle of oöcyte maturation is prevented if the median neurosecretory cells of the pars intercerebralis are cauterized, or if the corpora cardiaca are excised 24 hr before the onset of ecdysone synthesis in normal females. Implantation of additional brain-corpora cardiaca complexes into young vitellogenic females advances the time of ecdysone synthesis by some 12 hr. Oöcyte growth itself is not affected in these different types of experiments.It is inferred from the data of the present study that ecdysone synthesis in the follicle cell epithelium of maturing Locusta ovaries is stimulated by a neurohormone produced in the median neurosecretory cells of the pars intercerebralis and secreted into the blood via the corpora cardiaca.     

Studies on the neurosecretory system and retrocerebral endocrine glands of Nezara viridula Linn. (Heteroptera: Pentatomidae)

The neurosecretory system and retrocerebral endocrine glands of Nezara viridula Linn. have been described on the basis of in situ preparations and histological sections employing the paraldehyde fuchsin (PF) and performic acid-victoria blue (PAVB) techniques. In the brain of N. viridula, there are two medial groups–each consisting of five neurosecretory cells which belong to A-type. The lateral neurosecretory cells are absent. The axons of the two groups of medial neurosecretory cells (MNC) compose the two bundles of neurosecretory pathways (NSP) that decussate in the anterodorsal part of the protocerebrum. The two pathways, after the cross-over, run deep into the protocerebrum and deutocerebrum and emerge as NCC-I from the tritocerebrum. The nervi corporis cardiaci-I (NCC-I) of each side which are heavily loaded with NSM terminate in the aorta wall. Thus, the neurosecretory material (NSM), elaborated in the medial neurosecretory cells of the brain, is stored in the aortic wall and nervi corporis cardiaci-I (NCC-I). The NCC-II are very short nerves that originate from the tritocerebrum and terminate in the corpora cardiaca (CC) of their side. Below the aorta, but dorsal to the oesophagus, lie two oval or spherical corpora cardiaca. A corpus allatum (CA) lies posterior to the corpora cardiaca (CC). The corpora cardiaca do not contain NSM; only the intrinsic secretion of their cells has been occasionally observed which stains orange or green with PF staining method. The corpus allatum sometimes exhibits PF positive granules of cerebral origin. A new connection between the corpus allatum and aorta has been recorded. The suboesophageal ganglion contains two neurosecretory cells of A-type which, in structure and staining behaviour, are similar to the medial neurosecretory cells of the brain. The course and termination of axons of suboesophageal ganglion neurosecretory cells, and the storage organ for the secretion of these cells have been reported. It is suggested that the aortic wall and NCC-I axons function as neurohaemal organ for cerebral and suboesophageal secretions.     

Neuroendocrine regulation of corpus allatum activity in Manduca sexta: The endocrine basis for starvation-induced supernumerary larval moult

When newly-ecdysed 5th instar larvae of Manduca sexta were starved for 3 days and thereafter fed on standard diet the majority (90%) of the surviving larvae moulted into 6th instars. Allatectomy prior to starvation abolished the supernumerary moult, while denervation of the corpora allata (CA) had no effect.Cautery of medial neurosecretory cells, but not of the lateral cells, prevented supernumerary moulting and pupation ensued. Transplantation of brains from young 5th instar donors into larvae, whose medial neurosecretory cells were cauterized prior to starvation, restored the extra larval moult. Neither CA nor corpora cardiaca (CC) could be substituted for the medial neurosecretory cells.For induction of the supernumerary moult the medial neurosecretory cells are required only until day 1 after refeeding whereas the CA are required until day 3 after refeeding. Allatectomy on day 3 after refeeding resulted in the production of black 6th instar larvae.We conclude that starvation-induced supernumerary moulting is due to activation of the CA by allatotropin produced by medial neurosecretory cells in the brain. The anteromedial cells (group II) appear to be the source of allatotropin.     

Anti-juvenile effect of neuroparsin A,a neuroprotein isolated from locust corpora cardiaca

Neuroparsin A, a sulfur-containing protein synthesized by the medial part of the brain of Locusta and transported to the corpora cardiaca (CC) via the nervi corporis cardiaci I (Girardie et al., 1987), was satisfactorily isolated using electro-elution. A specific immune serum against electro-eluted neuroparsin A was generated. On serial histological sections of the brain treated with the immune serum, only the median neurosecretory cells [stained in blue following the double staining Victoria blue-paraldehyde fuchsin (Al type)] were revealed using peroxidase-antiperoxidase technique. Inactivation of neuroparsin A by antigen-antibody complex formation following injections of immune serum induced green pigmentation, intermediary forms and precocious sexual maturation. These symptoms also follow juvenile hormone (JH) injections. Injections of immune serum antineuroparsin A or the electro-eluted neuroparsin A produced opposite effects on oocyte growth but had no effect on the rate of JH biosynthesis evaluated by radiochemical assay. The neurohormone neuroparsin A could be the median humoral inhibiting factor of the JH system which was previously demonstrated (Girardie, 1966, 1967) in the central area of the pars intercerebralis.     

Hormone stimulated lipolysis and proline synthesis in the fat body of the adult tsetse fly, Glossina morsitans

G. morsitans fat cells incubated in vitro with l-[U-¹⁴C]-leucine incorporated the radiolabel, mainly into triglycerides. Aqueous extracts of corpora cardiaca, midbrain, or thoracic ganglion stimulated the release of radiolabelled material from prelabelled fat cells in vitro. Corpora cardiaca extracts were the most active, approx. 1 × 10^?3 gland pairs/μl elicited the maximal response. At concentrations above 1 × 10^?3 gland pairs/μl the activity of corpora cardiaca extracts was inhibited by a substance which could be removed by gel filtration. The stimulatory factor in nervous-tissue extracts was destroyed by proteolytic enzymes and was recoverable in a single peak by Sephadex G15 gel filtration. Results suggest that it is a peptide hormone produced mainly by the median neurosecretory cells of the midbrain with the corpora cardiaca being the site of storage and release. No hormone was detectable in fresh haemolymph, but it was found at high concentration in boiled haemolymph, implying the presence of a heat labile inhibitor.Under the in vitro conditions used the hormone stimulated the synthesis of proline from alanine and the hydrolysis of triglycerides to free fatty acids. The probable functions of the hormone are to stimulate proline synthesis in response to demand for flight and/or to mobilise lipid for larval nutrition. The relative importance of these apparent functions in vivo could not be determined.     

Characterization of three neurosecretory proteins from the A median neurosecretory cells of Locusta migratoria by coupled chromatographic,electrophoretic and isoelectrofocusing methods

Proteins from the nervous corpora cardiaca (N-CC) of Locusta migratoria were analysed using a combination of chromatography, electrophoresis and electrofocusing. Three major cysteine or/and cystine-rich proteins were identified as neurosecretory proteins of the median neurosecretory cells (M-NSC) by comparing the pattern of separated proteins of (1) intact N-CC and (2) depleted N-CC after intracerebral axotomy of the M-NSC.These three neurosecretory proteins are: a trimer, a dimer and a monomer. The trimer and the monomer are composed of apparent 18,000 subunits and 9000 polypeptide chains. The dimer is composed of apparent 7000 subunits composed of putative 4000 polypeptide chains. The three neurosecretory proteins are acidic (pH_i approx. 5.6 for the trimer, 5.1 for the monomer and 4.0 for the dimer). Their relationship to the neurophysins and to the neurosecretory protein isolated from brain and corpora cardiaca of the locust by Friedel et al. (1980) (Gen. comp. Endocr.41, 487–498) is discussed. The role of these three neurosecretory proteins (carrier protein, neurohormone or precursor of neurohormone) is as yet unknown.     

Côntrole neuroendocrine des protéines sanguines vitellogenes d'Anacridium aegyptium sain et parasite

The changing patterns of haemolymph proteins were followed in male and female adults of normal and parasitized Anacridium aegyptium during diapause (autumn, winter) or during activity (spring) of their endocrine system without or with electrostimulations of the pars intercerebralis (PI).The haemolymph protein concentration is high in winter and decreases in spring. It is comparatively depleted in locusts infected by the fly Metacemyia calloti. However, the depletion is significant only in ‘castrated’ females.Fifteen protein fractions were resolved by polyacrylamide disk gel electrophoresis in haemolymph of normal and infected locusts during diapause and activity. Some fractions decrease in quantity during activity in males, normal females, and parasitized females with complete ovarian development. One fraction disappears in females with mature eggs and seems correlated with formation of the eggshell. Eight others protein fractions exhibit electrophoretic mobility identical to the 7 protein fractions of homogenates of eggs. There is little doubt that these haemolymph protein fractions are involved in yolk synthesis and are thus ‘vitellogenic’. One of these ‘vitellogenic’ fractions (band 6) is larger in yolk than in blood.Five protein fractions were demonstrated by electrophoresis of homogenates of parasites. Their electrophoretic mobilities are similar to those of 5 of the 8 haemolymph ‘vitellogenic’ fractions of the host. There is little doubt that these 5 haemolymph protein fractions (one of them is the band 6) are involved in the nutritional requirements of the parasite.Electrostimulation of the PI, during diapause and activity, increase the haemolymph protein concentration and chiefly the protein concentration of the blood band 6. Thus, the median neurosecretory cells of the brain (M-NSC) regulate protein synthesis and chiefly the synthesis of ‘vitellogenic’ proteins.In parasitized females, the increase of the haemolymph protein concentration after electrostimulations of the PI is associated with an enhancement of ovarian development. The depletion of the haemolymph protein concentration in ‘castrated’ females is thus involved in the inability of the oöcytes to sequester available proteins from the haemolymph. The haemolymph protein deficiency may be attributed to (1) an impairment of protein synthesis, attendant upon the hypoactivity of the M-NSC, and (2) the nutritional requirements of the parasite.     

The role of central aminergic neurons in the action of 20-hydroxyecdysone on neurosecretory cells of Rhodnius prolixus

The enhancement of electrical activity of the neurosecretory cells in the brain and corpus cardiacum of Rhodnius prolixus induced by 20-hydroxyecdysone has been used as a means of examining the role of aminergic neurons in this reflex. The response of the brain and corpus cardiacum from mated ovariectomized females to 20-hydroxyecdysone was blocked by phentolamine and phenoxybenzamine (α-aminergic receptor antagonists) but not by propranolol (a β-aminergic receptor antagonist). Preparations taken from ‘reserpinzed’ females failed to respond to 20-hydroxyecdysone. Dopamine at 10^?7 M was capable of mimicking 20-hydroxyecdysone in activating the neurosecretory system from mated ovariectomised females as well as from ‘reserpinized’ mated ovariectomised females. The response to dopamine was blocked by phentolamine. The neurosecretory system from virgin ovariectomized females failed to respond to 10^?7 or 10^?6 M dopamine, but was activated by 10^?5 M dopamine.It is concluded that the action of 20-hydroxyecdysone onto the neurosecretory cells is indirect and involves aminergic interneurons. The results also suggest that the mating stimuli may function by enhancing the response of neurons to amines.     

Studies on the neurosecretory system of Ranatra elongata fabricius (Hemiptera: Nepidae) with reference to the distal fate of NCC I and II

With the help of PF and PAVB bulk-stained preparations and sections the neurosecretory system of Ranatra elongata has been described. Two medial, each of 9-10 cells, and two lateral, each of 3-4 cells, groups of neurosecretory cells have been observed in the protocerebrum. Only the A-cells have been found to be positive to PAVB histo- and cyto-chemical technique. Axons of the A-cells after traversing the proto- and deuto-cerebrum emerge from the tritocerebrum as the NCC I. The NCC I after bypassing the corpora cardiaca penetrate the aorta wall. There is no physical continuity between the corpora cardiaca and the NCC I and the two are separable. The NSM from the A-cells, transported by their nerve fibers, has been observed in the aorta wall. On the basis of large accumulation on NSM in the aorta wall the latter has been considered as the storage-and-release organ for the A-material. Corpora cardiaca are found to be devoid of A-material. Axons from the B-cells, after emergence from the tritocerebrum as the NCC II, have been observed to penetrate the corpora cardiaca. On the basis of ample amounts of B-material the glands have been considered as the storage-and-release organ for the B-material only. Observations are compared with results on related species and it is concluded that two independent organ complexes constitute the neurosecretory systemt of R. elongata. The A-cells, their pathways, the NCC I, and the aorta wall comprise the first; and the B-cells, their pathways, the NCC II, and the corpora cardiaca the second. The former is concerned with the elaboration, transportion, storage-and-release of the A-material and the latter with the B-material. Finally arguments are presented to include the aorta wall in the neurosecretory system.     

Age-dependent neurosecretion release induced by dopamine in the corpora cardiaca of Blattella germanica (L.) (Dictyoptera : Blattellidae)

In addition to glial cells, intrinsic glandular cells and ordinary axons, the corpora cardiaca of Blattella germanica (L.) (Dictyoptera : Blattellidae) contain 4 types of neurosecretory fibers originating from the brain (types 1, 2, 3, and 4), which can be recognized on the basis of the size, form, and electron density of their neurosecretory granules. A comparative ultrastructural study of the corpora cardiaca from normal females and from dopamine-treated (1 μg) females has been carried out at different stages within the first ovarian cycle (freshly emerged: day 0; 2-day-old: pre-vitellogenesis; 4-day-old: beginning of vitellogenesis; 6-day-old: full vitellogenesis; 8-day-old: post-vitellogenesis, period of ootheca transport). Quantitative data on the exocytotic configurations observed in each type of fiber (1–4) have led to the following conclusions: (a) the exocytotic configurations in control specimens are too infrequent to prompt any inference about the dynamics of neurosecretion release in the different types of fibers; (b) dopamine treatment induces a stimulation of the exocytotis phenomenon, whose extent depends on the specimen age and on the type of fiber. Therefore, on days 2 and 6, dopamine: preferentially stimulates neurosecretion release in the fibers of types 3 and 4 respectively.     

Neurosecretory cells in Dysdercus similis (Hemiptera)

The neurosecretory cells of Dysdercus similis have been described. "A", "B", "C" and "D" types of neurosecretory cells are present. The "A" type of cells of the pars-intercerebralis show cyclical secretion. When these cells show secretory activity during one to three days of emergence, they have scattered granules. The cells are seen packed with clumps of neurosecretory material when they are not secreting, and this is interpreted as a storage stage. The axons of these cells supply the corpora cardiaca and some neurosecretory material also reaches the corpus allatum. The release of this neurosecretory material can be correlated both with moulting in the young stages and later with reproduction in the adults.     

The Corpus Cardiacum Neurosecretory Cells of Schistocerca gregaria. Electron Microscopy of Resting and Secreting Cells

The corpora cardiaca of Schistocerca consist of a neurohaemal part containing mainly extrinsic neurosecretory axons coming from the brain, and of a glandular part consisting mainly of intrinsic neurosecretory cells. Some extrinsic axons penetrate into the glandular region, and innervate intrinsic corpus cardiacum neurosecretory cells. The fine structure of the latter has been examined and related to other neurosecretory cell types. Secretion occurs by exocytosis. Omega-profiles are more frequently observed in corpora cardiaca stimulated electrically or by acetylcholine than in the controls.     

Cockroach allatostatin-immunoreactive neurons and effects of cockroach allatostatin in earwigs

A monoclonal antibody to allatostatin I of the cockroach Diploptera punctata was used to demonstrate the presence of allatostatin-immunoreactive cells and fiber tracts in the neuroendocrine system of the earwig Euborellia annulipes. The corpora cardiaca cells were not immunoreactive, nor were the neurosecretory endings of fiber tracts from the brain to the corpora cardiaca. No immunoreactive material was detected in the corpus allatum, although the corpus allatum contained neurosecretory endings, and some cells of the brain, including medial and lateral protocerebral cells, showed immunoreactivity. In addition, the recurrent and esophageal nerves were allatostatin-positive. The last abdominal ganglion contained immunoreactive somata, and immunoreactive axons of the proctodeal nerve innervated the rectum, anterior intestine, and posterior midgut. We did not detect reactive endocrine cells in the midgut. Allatostatin I at concentrations of 10^–5 and 10^–7 M did not inhibit juvenile hormone biosynthesis by E. annulipes corpora allata in vitro. This was true for glands of low activity from 2-day females and brooding females, as well as for relatively high activity glands from 10-day females. In contrast, 10^–7 M allatostatin I significantly and reversibly decreased hindgut motility. Motility was decreased in hindguts of high endogenous motility from 2-day females and in those of relatively low activity from brooding females. These results support the notion that a primary function of allatostatin might be to reduce gut motility. Arch. Insect Biochem. Physiol. 38:155–165, 1998. © 1998 Wiley-Liss, Inc.     

Contribution à l'étude infrastructurale du système neurosécréteur rétrocérébral chez Locusta migratoria migratorioides (R. et F.)

Résumé L'étude infrastructurale des corpora cardiaca de Locusta révèle l'existence de 3 types de fibres neurosécrétrices (portion neurohémale) et d'un seul type de cellules glandulaires (portion endocrine intrinsèque). Elle permet également d'envisager les modalités du rejet des sécrétions exogènes et endogènes.

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Ultrastructural study of the retrocerebral neurosecretory system in Locusta migratoria migratorioides (R. et F.)I. The corpora cardiaca

Summary An ultrastructural study of the corpora cardiaca of Locusta migratoria migratorioides shows three neurosecretory fiber types in the neurohaemal part of these organs; only one cellular type constitutes the intrinsic glandular part of the corpora cardiaca. This study also shows sites of release of stored extrinsic neurosecretory material and of products elaborated by intrinsic glandular cells of the corpora cardiaca.

     

Intervention des cellules neurosecretrices medianes dans la castration parasitaire d'Anacridium aegyptium (Orthoptère)

The median neurosecretory cells (M-NSC) of Anacridium aegyptium were studied by light and electron microscopy during the ovarian diapause (autumn and winter) and the ovarian activity (spring) in normal females and in females infected by a tachinid fly Metacemyia calloti. In spring, the M-NSC contain comparatively much stainable material in normal females than in parasitized ones. This difference results from the ovarian maturity of normal females and the ovarian immaturity of parasitized females.The activity of the M-NSC was assessed in spring using the evolution of the radioactivity of the pars intercerebralis (PI) and corpora cardiaca (CC) after injection of ³⁵S-cysteine. The activity of the M-NSC is impaired in the parasitized females without ovarian development.The ovarian diapause was broken by massive implantations of corpora allata (CA) or electrical stimulations of the PI. Implantations of CA induce in parasitized females the same state of ovarian development than during natural activity in spring. Electrical stimulations of the PI. which increase the activity of the M-NSC. enhance the ovarian development of the parasitized females. A hypoactivity of the M-NSC is involved in the ‘castration’ of the Egyptian grasshopper.     

Methylxanthine inhibition of neurosecretion in the brain and corpus cardiacum of Cecropia

The fine-structure of the median neurosecretory cells and corpora cardiaca of the Cecropia silkmoth during the first 7 days after transfer from cold conditions to room temperature was compared to that of similar animals whose development was arrested with aminophylline. The major difference observed was the failure of the intrinsic secretory cells of the corpus cardiacum to degenerate in the arrested animals. This failure to degenerate coincides with the expected period of brain hormone release. After long periods of arrest, the medial neurosecretory cells and their axons became distended with neurosecretory granules. The significance of these observations in the initiation of adult development is discussed.