The chiasma-inducing pheromone of locusts

To the two quantitative criteria for phase transformation of locusts, viz. nymphal colour and adult morphometric ratios, the change in chiasma frequencies during meiosis in the male can now be added: gregarization or swarming induces an increase in chiasma formation. The atmosphere around crowded locusts contains a pheromone which is absorbed and causes a reactive haemolymph in locust hoppers. This haemolymph may be injected into solitarious hoppers or nymphs to induce increased chiasma formation. Certain solvents like risella oil and dimethyl sulphoxide will extract the pheromone from such an atmosphere, and bio-assays with these extracts have been demonstrated to be chiasma-inducing. Such extracts are, however, not chiasma-inducing in the albino mutant, but the haemolymph from crowded normal-coloured hoppers is reactive in the albino hopper. In addition the albino mutant is solitaria-like in both morphometric ratios and chiasma frequencies. These data indicate a relationship between the melanization cycle and chiasma induction: the previously postulated melanin-inducing pheromone and this chiasma-inducing pheromone are probably identical. On the other hand, this pheromone of nymphs and the sex-maturation pheromone of adults are not identical, although the latter may be a modified form of the other. The effect of the nymphal pheromone on adult morphometric ratios is not clear although some correlation has been shown to exist between raised chiasma frequencies in treated solitaries and advances towards gregaria ratios. It may be that in this pheromone we have, what may be called, a gregarizing principle.     

Genetic and environmental factors affecting chiasma formation in locusts

By means of crosses with the African Migratory locust it has been demonstrated that various strains carry different segregations of genes which quantitatively condition the formation of chiasmata during meiosis. These genes occur in polygenic series, and in one low frequency strain the polygenes show an epistatic effect for low chiasma frequency, while another low frequency strain seems to have attained this property through gamma radiation. In reciprocal crosses between the lastnamed low and a medium frequency strain there appears to be a maternal effect, with heterosis and epistasis respectively in the reciprocal crosses. In one strain two lines were selected for plasticity and non-plasticity of hopper colour change in small populations, and this selection has resulted in multiple changes in that the two lines now diverge in the three main physical criteria of phase transformation, viz. hopper colour, adult morphometric ratios and chiasma frequencies; one line is now solitarious for these characteristics, the other more gregarious. The genotypes selected out could be related to the ability to utilize the gregarization pheromone.A 10° rise in temperature above 22° C has the effect of increasing chiasma frequencies significantly, but increase in the carbon dioxide content of the atmosphere has no effect. Male and female hoppers produce equivalent amounts of the chiasma-inducing pheromone, while solitarised hoppers do not lose the ability to produce this pheromone. The crucial stage for the action of this pheromone on chromosomes is during the fifth nymphal instar. The phase status of parents appears to affect chiasma frequencies in the offspring, more specifically that of the mother, so that there is further evidence of maternal effect on chiasma frequency.     

Secretion of Dopa in Phaeochromocytoma

In a series of 11 cases with phaeochromocytoma, two patients were found in whom the tumour secreted dopa in addition to dopamine, noradrenaline, and adrenaline. These two patients were normotensive in spite of high plasma and urinary levels of noradrenaline and adrenaline. This raises the possibility that dopa may be able to protect against the hypertensive action of noradrenaline. Such a mechanism would also explain the absence of hypertension in many cases of neuroblastoma.     

The action of locustol

Bioassays have shown that the locust gregarization pheromone, locustol, and the adrenergic hormone, noradrenaline, act in a similar way on the phase characteristics of the locust and are thus mimics. Investigations of the affects of dopa (a noradrenaline substrate) and its antagonist aldomet, and of the effects of adenosine 3′–5′ monophosphate (cyclic AMP), its agonists and antagonists, as well as an assay of cyclic AMP in the two phases, have strengthened this conclusion. It is postulated that the pheromone acts like an adrenergic hormone to promote the production of cyclic AMP which effects the characteristic changes when the solitary phase of locusts transforms into the gregarious phase.     

Inactivation of creatine kinase induced by dopa and dopamine in the presence of ferrylmyoglobin

We investigated the effect of dopa and dopamine on creatine kinase (CK) activity in the presence of ferrylmyoglobin (ferrylMb). CK was sharply inhibited by dopa and dopamine in the presence of ferrylMb. Dopa and dopamine markedly promoted the reduction of ferrylMb to metmyoglobin (metMb). The semiquinone from dopa and dopamine may be involved in CK inactivation. During inactivation of the enzyme, both kinetic parameters Vmax and Km changed. In addition, reduced glutathione restored the activity of CK at an early stage. These results suggest that inactivation of CK is dominantly due to oxidation of sulfhydryl (SH) groups of the enzyme. Other catechols, such as adrenaline and noradrenaline, little inactivated CK activity, whereas they promoted the reduction of ferrylMb to metMb. Other SH enzymes, including alcohol dehydrogenase (ADH) and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), were inactivated to a lesser extent by dopa and dopamine in the presence of ferrylMb. Adrenaline and noradrenaline did not significantly prevent the inactivation of ADH and very slightly inhibited GAPDH. These results suggest that dopa and dopamine act as prooxidants to inactivate SH enzymes in the presence of ferrylMb.     

Modulation of cerebral catecholamine concentrations during hyperphenylalaninaemia.

Hyperphenylalaninaemia induced by daily injections of alpha-methylphenylalanine plus phenylalanine caused 20-40% decreases in cerebral dopamine (3,4-dihydroxyphenethylamine) and noradrenaline in 7- and 11-day-old rats. alpha-Methylphenylalanine alone as well as phenylalanine alone caused cerebral dopamine depletion. However, the effects were not additive, in that the depletion caused by alpha-methylphenylalanine was greater, not less, than that after treatment with both it and phenylalanine. Increased concentrations of tyrosine in the brain, owing to administered or endogenously formed tyrosine, could overcome the effect of excess phenylalanine on cerebral dopamine content. The fact that the inhibition of tyrosine hydroxylase by phenylalanine (or alpha-methylphenylalanine) in vitro was overcome by tyrosine concentrations similar to those effective in vivo further implicates the tyrosine hydroxylase inhibition as the mechanism underlying the dopamine depletion in hyperphenylalaninaemia. These results provide a theoretical basis for elevation, by tyrosine supplementation, of the cerebral phenylalanine/tyrosine ratio as a possible treatment modality for phenylketonuria.     

Catecholamine biosynthesis in vitro and in vivo in the chromaffin tissue of the Atlantic cod, Gadus morhua

1. The biosynthesis of [3H]catecholamines from [3H]L-tyrosine in the intact chromaffin tissue of cod posterior cardinal veins was studied in vitro and in vivo at 10 degrees C. 2. The tritiated products dopamine, noradrenaline and adrenaline were separated from the [3H]tyrosine by paper chromatography of tissue extracts and the radioactivity of 1 cm strips of the chromatogram was determined by liquid scintillation spectrophotometry. DOPA could never be demonstrated in the tissue extracts from any of the experiments performed. 3. The content of [3H]noradrenaline in pieces of the cardinal veins incubated in vitro was found to increase rapidly. The tissue content of dopamine and adrenaline remained at lower levels which were reached during the first few hours of the incubation. A similar pattern could be demonstrated in the chromaffin tissue in vivo after infusion of [3H]tyrosine, but the total content of the [3H]catecholamines was lower than in the in vitro experiments. 4. The results are consistent with the view that the methylation of noradrenaline is the rate-limiting step in the biosynthesis of adrenaline in cod chromaffin tissue.     

Kinetics of the effect of noradrenaline, dopa and dopamine on the glycemia of bees in vivo

Following intra-abdominal injection of noradrenaline, dopamine and dopa to living workerbees, an increase of haemolymph glucose occurred respectively after 30 min, 90 min and 120 min. In each case the trehalose first undergoes a slight increase within 30 to 45 min followed by a more important decrease becoming significant after 2 to 3 h. The kinetics effects of noradrenaline on glucose look very close to those of adrenaline, while the other two precursors seem to wear an hyperglycaemic action only after their conversion into an active form.     

PHEROMONES AND CHEMICAL ECOLOGY OF LOCUSTS

Modern studies of chemical ecology and behaviour of the locusts Schistocerca gregaria and Locusta migratoria in the laboratory need to be more closely coupled with field experiments and observations. The life history relating to oviposition, transformation to gregarious phases, and adult maturation mediated by pheromones is reviewed. The principles of pheromone isolation and identification are discussed. The long-term effects of the gregarization pheromone on the physiology are presented, with discussion of morphological changes, chiasma frequency increases, and synchronization of moulting induced by the pheromone. Isolation of the purported gregarization pheromone, locustol, from faeces is discussed in regard to inconsistent effects. Other more immediate effects of the pheromone on the social (gregarious) behaviour and the isolation of possible pheromone components different from but related to locustol are presented. It is stressed that more rigorous isolation studies should be undertaken to resolve conflicting reports and methodological problems. The possibility of an anti-gregarization pheromone or solitarizing pheromone is discounted. The source and biosynthesis of locustol (or gregarization pheromone) from degradation of lignin by symbiotic bacteria is discussed. Theories of reception of the gregarization pheromone such as inhalation through the spiracles or sensory perception by the antennae are presented. Also an internal mechanism involving cAMP and/or corpora allata may be induced by gregarization pheromone to effect the physiological phase changes. The advantages to an individual of reception of the gregarization pheromone from a group of gregarious and pre-migrating locusts is discussed. Also the possible benefits of gregarious behaviour, phase polymorphism and migration are dealt with. An adult (sexual) maturation pheromone has long-term effects on reducing the period of maturation, and immediate effects on the behavioural vibration response. The epidermal source of the pheromone and glandular cells responsible for the production of the pheromone are discussed. The reception and internal mechanisms of response via the corpora allata are mentioned. The benefits to individuals of synchronized and rapid adult maturation in a gregarious group are considered. An oviposition-stimulating pheromone produced by the male accessory reproductive glands appears to be a proteinaceous substance of large molecular weight. On the other hand, an oviposition-aggregating pheromone volatilizes from epidermal areas of either sex and causes higher oviposition rates in the area of release. The behavioural and ecological aspects of this pheromone are discussed. Several other possible pheromones and semiochemicals are discussed, such as a long-range sex pheromone, sex-recognition pheromone, grass odours and feeding stimulants and deterrents. Several possible control strategies using locust pheromones are considered. The general conclusion is that the chemical isolation of the various pheromones is necessary before further progress can be achieved on the source and biosynthesis of pheromone, reception of pheromone, behavioural effects of pheromone, and control measures.     

Locustol and its analogues

A new method of synthesis of the locust gregarization pheromone, locustol, is described, the pathway being from guaiacol to acetyl-isoacetovanillone, to isoacetovanillone, to 5-ethylguaiacol. These substances were all checked for their infrared spectra and were bioassayed. Only 5-ethylguaiacol affected chiasma frequency, hopper colour, and the $\text{F}\text{C}$ morphometric ratio, although guaiacol had some effect on chiasma frequency. Hopper and adult faeces, as well as grasshopper faeces, were steamextracted, tested by infrared spectrophotometry and by gas chromatography, and were bioassayed. Only the hopper faeces extract contained the pheromone as well as some isoacetovanillone. In the adult and grasshopper faeces extracts no aromatic substance could be found but the impurities contained, possibly, a mixture of a secondary alcohol, a carboxylic acid, and/or its ester, some of which also occurred in the impure hopper faeces extract. Isovanillin, 5-methylguaiacol, and amylacetate were also bioassayed: they showed no effect on chiasma frequencies, but the latter stimulated the production of a gregaria $\text{F}\text{C}$ ratio in solitaries. A figure is given of the chemical structures of eight substances which are part-analogues of locustol in regard to chiasma frequency, and of eight related substances which are chromosomally inactive but of which amylacetate stimulates the gregaria $\text{F}\text{C}$ ratio and methylformate stimulates the production of black hopper colour in solitaries. A consideration of these structures may aid in solving the chemical action of locustol.     

An automated fluorometric method for the estimation of dopamine in brain tissue extracts

A method for the automated estimation of dopamine in the concentration range of 10–2000 ng/ml is presented which can process 30 samples/hour with an average error of 0.87%. Interference by dopa is high. Interferences by noradrenaline and adrenaline are 0.6 and 0.5%, respectively, and can normally be neglected. Dopamine contents of striata of controls and of α-methyltyrosine-treated rats were estimated with this system.     

Catecholamine levels in whole brain of stressed and control domestic and wild rats (Rattus Norvegicus)

Whole brain catecholamine (dopamine, nonadrenaline, adrenaline) levels were measured in control and electric footshocked Wild and domestic (Sprague Dawley and Long Evans) rats. No significant differences were found among the three strains of rats for combined total catecholamine content, or for combined total catecholamines between the control and footshocked groups. Significant differences were found for the total of each catecholamine taken separately, dopamine being present at three times the level of noradrenaline and ten times the level of adrenaline. No significant differences were found for dopamine in both control and footshocked animals among all three rat strains. Noradrenaline was significantly higher in the control domestic rats compared to the control Wild rats, and in the footshocked domestic rats compared to the footshocked Wild rats. No differences in noradrenaline levels were found between Sprague Dawley and Long Evans rats, but noradrenaline increased significantly in the latter following footshock. Adrenaline was significantly highest in the Sprague Dawley controls and lowest in the Wild controls. Footshocking resulted in almost identical levels of adrenaline in the domestic strains and an increase in the F₁ Wild strain.     

The synthesis of noradrenaline by isolated guinea-pig atria

1. The initial rate of formation of noradrenaline by isolated atria from a physiological concentration of tyrosine was measured. 2. Study of the time-course of the formation led to the conclusion that newly formed noradrenaline enters a fraction of the total pool. Synthesis and turnover was maintained for at least 1·5hr. In this time it was not possible to increase the concentration in the storage pool by employing high concentrations of precursor. 3. Preincubation of the tissue with noradrenaline resulted in an accumulation within the tissue and inhibited new formation. It is suggested that this indicates the existence of a physiological mechanism to limit the synthesis of noradrenaline, avoid saturation of storage sites and enable the `re-uptake' process to operate. 4. The amount of noradrenaline formed from 3-hydroxytyramine (dopamine) was considerably greater than from tyrosine. The kinetic constants of the reactions are in agreement with the view that hydroxylation of tyrosine to dihydroxyphenylalanine (dopa) is rate-limiting.     

The hydroxylation of phenylalanine and tyrosine: a comparison with salicylate and tryptophan.

The hydroxylation of phenylalanine by the Fenton reaction and gamma-radiolysis yields 2-hydroxy-, 3-hydroxy-, and 4-hydroxyphenylalanine (tyrosine), while the hydroxylation of tyrosine results in 2,3- and 3,4-dihydroxyphenylalanine (dopa). Yields are determined as a function of pH and the presence or absence of oxidants. During gamma-radiolysis and the Fenton reaction the same hydroxylated products are formed. The final product distribution depends on the rate of the oxidation of the hydroxyl radical adducts (hydroxycyclohexadiene radicals) relative to the competing dimerization reactions. The pH profiles for the hydroxylations of phenylalanine and tyrosine show a maximum at pH 5.5 and a minimum around pH 8. The lack of hydroxylated products around near pH 8 is due to the rapid oxidation of dopa to melanin. The relative abilities of iron chelates (HLFe(II) and HLFe(III) to promote hydroxyl radical formation from hydrogen peroxide are nitrilotriacetate (nta) greater than ethylenediaminediacetate (edda) much greater than hydroxyethylethylenediaminetriacetate greater than citrate greater than ethylenediaminetetraacetate greater than diethylenetriaminepentaacetate greater than adenosine 5'-triphosphate greater than pyrophosphate greater than adenosine 5'-diphosphate greater than adenosine 5'-monophosphate. The high activity of iron-nta and -edda chelates is explained by postulating the formation of a ternary Fe(III)-L-dopa complex in which dopa reduces Fe(III). The hydroxylations of phenylalanine and tyrosine are similar to that of salicylate (Z. Maskos, J. D. Rush, and W. H. Koppenol, 1990, Free Radical Biol. Med. 8, 153-162) and tryptophan (preceding paper) in that oxidants augment the formation of hydroxylated products by catalyzing the dismutation of hydroxyl radical adducts to the parent compound and a stable hydroxylated product. A comparison of salicylate and the amino acids tryptophan, phenylalanine, and tyrosine clearly shows that salicylate is the best indicator of hydroxyl radical production.     

Enkephalins and the function of the sympathetic-adrenal system in acute myocardial ischemia

It has been shown in experiments on albino rats that acute myocardial ischemia (AMI) produces a noticeable increase in excretion of adrenaline, noradrenaline, DOPA and dopamine with urine. Intraperitoneal injection of leu-enkephalin analogs (D-Ala2-Leu5-Arg6 and D-Ala2-D-Leu5-D-Arg6) to rats with AMI was accompanied by a noticeable prevention of activation of the sympathoadrenal system.     

Abundance in the Embryonic Brainstem of Adrenaline During the Absence of Detectable Tyrosine Hydroxylase Activity

The activities of the catecholamine synthetic enzymes tyrosine hydroxylase and phenylethanolamine N-methyltransferase, and the concentrations of the catecholamines and their respective metabolites, have been measured in the dorsal and ventral halves of the brainstem at various ages in the embryonic and adult rat. The activity of phenylethanolamine N-methyltransferase in both parts of the brainstem at day 14 of gestation is at or greater than adult levels and thereafter displays relatively small variations during ontogeny. Tyrosine hydroxylase activity, in contrast, is undetectable at day 14 and increases slowly, achieving only 20-25% of adult values by day 18 of gestation. Adrenaline concentrations correlate well with the activity of phenylethanolamine N-methyltransferase, showing a precocious development, whereas noradrenaline and 3,4-dihydroxyphenylethylamine (dopamine) concentrations are more closely related to the enhancement of tyrosine hydroxylase activity; at day 18 of gestation, for example, they are only 5 and 10%, respectively, of the adult values. The concentrations of the metabolites of noradrenaline and dopamine are suggestive of a high rate of turnover. These results confirm previous immunocytochemical evidence of a tardy appearance of tyrosine hydroxylase-like immunoreactivity in the phenylethanolamine N-methyltransferase-positive perikarya of the embryonic medulla oblongata. In addition, the abundance of adrenaline in this area at early gestational stages strongly suggests that, despite the paucity of tyrosine hydroxylase, phenylethanolamine N-methyltransferase is active in vivo and is utilizing a substrate other than noradrenaline. It is likely, however, that at later stages of gestation, when tyrosine hydroxylase is present at sufficient activity to supply noradrenaline, the conventional synthetic pathway for adrenaline formation comes into being.     

Caffeine Ingestion by Rats Increases Noradrenaline Turnover and Results in Self-Biting

The effects of caffeine on the activity of central and peripheral catecholaminergic structures have been studied in rats ingesting high doses of caffeine. The activities of the enzymes tyrosine hydroxylase and dopamine-beta-hydroxylase were measured as well as 3,4-dihydroxyphenylethylamine (dopamine), adrenaline, and noradrenaline concentrations, in brain (striatum and hypothalamus), heart, and adrenal gland. At the peripheral level, we observed a significant increase in the dopamine and adrenaline plus noradrenaline content in the heart, but an increase in dopamine content only was found in the adrenal gland. Dopamine-beta-hydroxylase activity in serum was increased, but the only significant enzymic change in brain was an increase in the dopamine-beta-hydroxylase activity of the hypothalamus. However, an increase in catecholamine content was observed in both structures of the brain. These data suggest that the mechanisms involved in caffeine-induced self-biting in rats are not limited to the dopaminergic system, because we have also observed an increase in noradrenaline turnover.     

Tyrosine administration decreases serum prolactin levels in chronically reserpinized rats

The injection of tyrosine, 200 mg/kg, decreased serum prolactin levels and elevated hypothalamic (and striatal) concentrations of two dopamine metabolites, dihydroxyphenylacetic acid and homovanillic acid, in chronically reserpinized rats. Tyrosine administration had none of these effects in otherwise untreated rats, and did not block the increase in serum prolactin that occurred 4 hours after a single injection of reserpine. As anticipated, the injection of dopa decreased serum prolactin in all rats. Valine, another large neutral amino acid, did not modify serum prolactin in chronically reserpinized animals. Since prolactin secretion is normally inhibited by dopamine released from the hypothalamus, reserpine treatment probably elevates serum prolactin by depleting the hypothalamus of dopamine. Our data suggest that tyrosine injection suppresses serum prolactin levels in chronically reserpinized rats by enhancing the synthesis and release of hypothalamic dopamine. Thus, administration of tyrosine, dopamine's dietary precursor, can alter physiologic functions that depend on dopamine.     

Tyrosine and catecholamine metabolism in wild-type Drosophila melanogaster and a mutant, ebony

Microinjection of radioactive tyrosine, dopa, and dopamine into mature larvae of Drosophila revealed that the sclerotization pathway is similar but not identical to that in Calliphora: (a) tyrosine is converted to tyrosine-o-phosphate and not to dopa, and (b) the substrate N-acetyldopamine does not accumulate.Larvae of the mutant ebony appear to be similar to the wild type with respect to tyrosine, dopa, and dopamine utilization. About the time of eclosion, however, ebony has twice as much dopamine as normal. Some implications of this are discussed with reference to the mutant phenotype.