Synthesis and biological activity of adipokinetic hormone analogues modified at the C-terminus

A series of Locusta adipokinetic hormone I (AKH-I), C-terminal threonine residue using a combination of solid- and liquid-phase methodology and evaluated in Locusta migratoria, in a lipid mobilization assay in vivo and an acetate uptake assay in vitro. Modifications at Thr¹⁰ of AKH-I involved replacement of its C-terminal amide by the groups -OH, -OCH₃, -NHCH₃, -N(CH₃)₂, and -NHC₆H₅; the last three groups were also applied to the amide of AKH-I-[Thr(Brl)¹⁰]. The methyl ester, monomethyl, and dimethyl analogues were all of lower activity than the parent in the lipid mobilization assay, but lost less than two orders of potency. In the acetate uptake assay, again the methyl ester analogue showed the greatest retention of biological activity of all modified peptides. A cyclic analogue, cyclo (PLNFTPNWGT), was active in both assay, but only at very high concentrations. Almost all analogues were more active in the acetate uptake assay than in the lipid assay, but unusually, AKH-I-NHCH₃ and AKH-I-N(CH₃)₂, together with cyclo (PLNFTPNWGT), were more active in the lipid mobilization assay. In addition, the acid AKH-I analogue did not suffer as large a loss in potency in the lipid mobilization assay as in the acetate uptake assay, although it was less potent in the former. The relative potencies of these two methyl analogues contrast with those for AKH AKH-I-[Thr(Bzl)¹⁰]-NHCH₃ and AKH-I-[Thr(Bzl)¹⁰]-N(CH₃)₂, which, together with both phenyl analogues, were significantly more active in the acetate uptake assay. We conclude that the acetate uptake assay has a greater preference for a hydrophobic C-terminus, compared with the lipid mobilization assay.     

Potencies of naturally-occurring AKH/RPCH peptides in Locusta migratoria in the acetate uptake assay in vitro and comparison with their potencies in the lipid mobilisation assay in vivo

The biological potencies of a number of naturally-occurring octa- and decapeptides of the large AKH/RPCH family of peptides were determined in Locusta migratoria using the lipid-mobilising assay in vivo and the acetate uptake assay in vitro. The most potent of the newly-tested peptides in the in vitro assay, Phl-CC, differs from the endogenous major locust peptide, Lom-AKH-I, only by an exchange of serine versus threonine at position 10. However, the most active peptide in the in vitro assay remains Lom-AKH-III. At the other extreme is the peptide Mem-CC which contains a tyrosine residue at position 4 rather than the more typical phenylalanine. This peptide is over 20,000 times less potent than Lom-AKH-III in the in vitro assay, and also results in an unusual dose-response curve in the in vivo assay. Only a few peptides are approximately equipotent in both assays, but mostly the bioanalogues have a higher potency in vitro. The majority of them are 2- to 10-fold more potent in vitro, but Ani-AKH and Lom-AKH-III are 19- and 48-fold more potent. The results are discussed in relation to either the actions of proteases or of possible preferential binding of different receptors involved in the different assays.     

The effects of allatectomy and ovariectomy on haemolymph proteins and lipid mobilization in Locusta

After ovariectomy the concentrations of diacylglycerol and protein in the haemolymph increase markedly. The increased diacylglycerol is associated with increased quantities of the ‘heparin-precipitable’ protein (lipoprotein A) that carries diacylglycerol in the blood of normal resting locusts. After the injection of adipokinetic hormone (AKH), the blood of ovariectomized locusts contains only slight quantities of the ‘heparin-soluble’ lipoprotein A⁺ whereas this forms in large amounts in the blood of sham-operated locusts after AKH injection. After allatectomy, the increase in the adipokinetic response is slower and the full level of responsiveness observed in sham-operated locusts is never attained. Nevertheless, allatectomized locusts develop a marked adipokinetic response which tends to stabilize as they age; it does not deteriorate as it does in aged sham-operated locusts.The effects of ovariectomy on blood metabolites can be prevented completely by allatectomy, but only partially by cautery of the cerebral neurosecretory cells. Treatment with a juvenile hormone analogue (JHA R-20458) counteracts the effects of allatectomy in ovariectomized locusts.     

Locust haemolymph lipoproteins visualised in the electron microscope

Summary In matureLocusta, the haemolymph lipoproteins change both in quality and quantity according to the physiological state of the animal. In resting locusts the majority of lipid in the haemolymph is carried by lipoprotein A_yellow, but during flight or after adipokinetic hormone injection, A_yellow joins together with extra diacylglycerols from the fat body and non-lipid carrying C_L-proteins to form another lipoprotein, A⁺. In this study partially purified A_yellow and A⁺ lipoproteins have been visualised by transmission electron microscopy after negative staining or shadowing. Both A_yellow and A⁺ lipoproteins are discrete particulate structures but they differ markedly in size; A_yellow particles are 9–16 nm in diameter while those of A⁺ are mostly in the range 20–50 nm. Large lipoprotein particles of the A⁺ type have not been described previously in insect haemolymph but, interestingly, the locust A⁺ particles do resemble most closely the low density lipoprotein particles described in human serum by Forte and Nichols (1972).     

Diglyceride-transporting lipoproteins inLocusta

Summary The majority of haemolymph proteins obtained from resting mature locusts are soluble in 50% saturated (NH₄)₂SO₄ solution. Chromatographically, these proteins may be resolved on Sepharose 6B into three partially included fractions. The leading high molecular weight fraction, A, is predominant and all the diglyceride in resting blood is associated with it. An additional higher molecular weight fraction, A⁺, is present in the haemolymph of locusts injected with extracts of the glandular lobes of the corpora cardiaca (elevated blood), and this fraction carries all the increased diglyceride. Fraction A⁺ is better resolved on Ultrogel ACA 22. A useful rapid technique for studying the formation of A⁺ lipoprotein during lipid mobilization has been developed by the use of lipoproteinpolyanion-metal ion complex formation. A⁺ is soluble after heparin treatment whereas the yellow leading edge of fraction A precipitates. Concomitant with the appearance of A⁺ there is a marked depletion of a lower molecular weight non lipid-carrying protein fraction, C. The ability to form fraction A⁺ after injections of glandular lobe extract cannot be demonstrated in fledglings (immature locusts within 2 or 3 days after the imaginal moult) where fraction C is virtually absent. It is suggested that during lipid mobilization, some lipoprotein from fraction A combines with protein from fraction C to form A⁺. A direct effect of adipokinetic hormone on the process of A⁺ formation cannot be excluded.     

Some effects of mermithid infection on metabolic reserves and flight in Locusta

Low infections of Mermis nigrescens reduce the flight performance of adult male Locusta migratoria, and bring about changes in the levels of blood carbohydrate and protein but not lipid. The quantities of all three metabolites in the fat body are reduced, as is the amount of tissue present. Lipid content only, is markedly decreased in the flight muscle, but the water content is increased.

Blood volume and malpighian tubule activity are unaffected by mermithid infection, but the rates of lipid mobilisation in response to injections of extracts of corpora cardiaca or flight are greatly reduced compared with those in uninfected locusts. Additional carbohydrate does not correct flight performance in parasitised locusts as it does in starved animals. Poor flight performance is not due to an effect of the worm on the host endocrine system.     

The effects of corpora cardiaca on tethered flight in the Locust

Summary Removal of the cerebral neurosecretory cells tas no effect on the tethered flight pattern of adult maleLocusta. However, the flight pattern is markedly influenced by removal of the glandular lobes of the corpora cardiaca or by injection of 0.01 pair of corpora cardiaca. Changes in flight speed, brought about by such injections, may reflect differences in substrate utilisation in response to hormonal factor(s) from the corpora cardiaca. It is suggested that one effect of corpus cardiacum factor(s) may be the suppression of carbohydrate utilisation by the flight muscles.     

A new member of the AKH/RPCH family that stimulates locomotory activity in the firebug, Pyrrhocoris apterus (Heteroptera)

A new member of the AKH/RPCH family was isolated and identified from the corpora cardiaca of the firebug Pyrrhocoris apterus. The peptide was isolated in a single step by reversed phase HPLC and the structure deduced from the multiple MS (MS(N)) electrospray mass spectra and amino acid analysis as that of an octapeptide with the sequence pGlu-Leu-Asn-Phe-Thr-Pro-Asn-Trp-NH(2): this sequence was confirmed by synthesis. The synthetic peptide induced lipid mobilisation and stimulated locomotory activity in macropterous females. This peptide, designated as Pyrrhocoris apterus adipokinetic hormone (Pya-AKH), is the first identified adipokinetic hormone described in a representative species of the suborder Heteroptera.     

Variation in the mitochondrial control region in the Juan Fernández fur seal (Arctocephalus philippii)

The Juan Fernandez fur seal (Arctocephalus philippii was allegedly extremely abundant, numbering as many as 4 million prior to sealing which continued from the late 17th to the late 19th century. By the end of the sealing era the species was thought to be extinct until they were rediscovered at Alejandro Selkirk Island in 1965. Historic records would suggest that the species underwent a substantial population bottleneck as a result of commercial sealing, and from population genetic theory we predicted that the genetic variability in the species would be low. We compared the mtDNA control region sequence from 28 Juan Fernandez fur seals from two islands in the Juan Fernandez Archipelago (Chile). Contrary to expectation, we found that variation in the Juan Fernandez fur seals is not greatly reduced in comparison to other pinniped taxa, especially given the apparent severity of the bottleneck they underwent. We also determined minor, but significantly different haplotype frequencies among the populations on the two islands (Alejandro Selkirk and Robinson Crusoe Islands), but no difference in their levels of variability. Such differences may have arisen stochastically via a recent founder event from Alejandro Selkirk to Robinson Crusoe Island or subsequent genetic drift.