Energy homeostasis is essential for organisms to maintain fluctuation in energy accumulation, mobilization. Lipids as the main energy reserve in insects, their metabolism is under the control of many physiological program. This study aimed to determine whether the adipokinetic hormone receptor (AKHR) was involved in the lipid mobilization in the Spodoptera litura. A full-length cDNA encoding AKHR was isolated from S. litura. The SlAKHR protein has a conserved seven-transmembrane domain which is the character of a putative G protein receptor. Expression profile investigation revealed that SlAKHR mRNA was highly expressed in immatural stage and abundant in fat body in newly emerged female adults. Knockdown of SlAKHR expression was achieved through RNAi by injecting double-stranded RNA (dsRNA) into the 6th instar larvae. The content of triacylgycerol (TAG) in the fat body increased significantly after the SlAKHR gene was knockdown. And decrease of TAG releasing to hemolymph with increase of free fatty acid (FFA) in hemolymph were observed when the SlAKHR gene was knowned-down. In addition, lipid droplets increased in fat body was also found. These results suggested that SlAKHR is critical for insects to regulate lipids metabolism.

The main cell types of the adult bee fat body are trophocytes and oenocytes; however, in pupae of some newly emerged bees, trophocytes are modified into cells called urocytes, which possibly function as a substitute for Malpighian tubules during metamorphosis when larval tubules are not functional and/or storage of urate salts is required. This study evaluated the morphology of urocytes in the stingless bee Melipona quadrifasciata and the possibility of maintaining these cells in primary culture. The urocytes M. quadrifasciata are white spherical cells with an irregular surface as observed by stereomicroscopy. They may be found individually or in groups associated with tracheae. Urocytes have a single, small, and spherical nucleus and cytoplasm rich in neutral polysaccharides, lipid droplets, protein, and granules containing calcium and urate salts. Our findings suggest that urocytes play a role in storage of neutral polysaccharides and calcium in M. quadrifasciata pupae and that these cells can be cultured for 72 h.

Vitellogenin synthesis by the fat body has been monitored using in vitro culture and immunoprecipitation. This system was found to be efficient for measuring vitellogenin production in both non-infected Tenebrio molitor and those infected with Hymenolepis diminuta. In fat bodies from infected beetles, vitellogenin production was decreased by up to 75% (day 24 post-infection) and, at all times investigated, vitellogenin synthesis was significantly below control levels (days 3–30 post-infection). Incubating fat bodies from control insects with isolated metacestodes indicated that this may be a direct effect by the parasite which is developmental stage-specific. Stage II, but not stage III–IV, nor heat-killed parasites could bring about this decrease in vitellogenin. In addition, these effects may be density dependent within the range of 2–20 parasites per fat body; only 2 metacestodes were necessary to cause a significant decrease. Since metacestodes do not take up vitellogenin, nor limit the amount of [14C] leucine available to the fat body for vitellogenin production, it is conceivable that the parasite produces a potent inhibitor of vitellogenin synthesis, or a molecule which induces cells within the fat body to do so.

The metamorphosis of oncospheres of the rat tapeworm, Hymenolepis diminuta, to mature metacestodes induces several pathophysiological effects in the intermediate host, Tenebrio molitor (Coleoptera). Previous investigations have failed to elucidate the mechanism responsible for changes in the host reproductive physiology and behaviour. This work forms part of an assessment of the degree to which nutrient resource management may be involved in these interactions. We report that developing metacestodes exert a pronounced effect upon host carbohydrate reserves and also alter circulating carbohydrate titres at some stages post-infection. Biochemical studies of fat body glycogen demonstrated a significant depletion of reserves as early as 3 days post-infection in males and 5 days post-infection in females. Gas chromatography revealed trehalose to be the predominant haemolymph carbohydrate, titres being significantly elevated in male beetles 5 and 9 days post-infection and in females 12 days post-infection. Metacestodes had no effect on glucose concentrations in male or female beetles.

The levels of lipophorin, the principal insect haemolymph lipoprotein, were estimated during the development of solitary and gregarious phases of Schistocerca gregaria using single radial immunodiffusion. In the gregarious phase, lipophorin titres ranged from 6.69 ± 0.57 mg/ml in the 3rd nymphal instar to 14.42 ± 2.04 mg/ml in mature adults. The titres in the solitary phase were 3.33 ± 0.59 mg/ml in the 3rd nymphal instar and 8.44 ± 0.67 mg/ml in mature adults. Peak lipophorin titres occurred in mature adults (14.42 ± 2.04 mg/ml) and 5th nymphal instar (8.75 ± 0.25 mg/ml) for gregarious and solitary locusts, respectively. Gregarious locusts had significantly (P< 0.05) higher lipophorin titres than their solitary counterparts during the 3rd and 4th nymphal instars as well as in the adult stage (P< 0.01). Estimation of the haemolymph protein levels over the same period showed a general increase from the 3rd nymphal instar to mature adult stage in both phases. It is proposed that the higher lipophorin titre in gregarious locusts is a physiological adaptation that ensures high lipid reserves that are necessary to cope with the high metabolic requirements of this phase.

Eucalyptus oil vapour treatment provided to Dysdercus koenigii female individuals as virgin adults or during their fifth instar nymphal life led to a fall in the total protein content accompanied by a rise in the free amino acid titre of haemolymph and fat body. However, the level of total lipids in these two tissues under such condition varied in that a decrease and an increase were recorded in haemolymph and fat body respectively. In the ovary of this adult female, the amounts of total proteins and lipids were low, while the value for total free amino acids was high. The implications of all these findings are discussed chiefly in relation to transport, synthesis and degradation of biochemical constituents in the three tested tissues.

The fat body protein content of silkworms increased with 0.5 μg of thyroxine (T4) per gram of body weight and more so with 1 μg/g on days 4 and 8 after injection. Thyroxine with 1 μg/g dose, however, caused an earlier increase in protein content on day 2. The higher doses of T4 (2 and 5 μg/g) decreased the protein content. All T4 treated groups (except with an ineffective dose of 0.25 μg/g) showed reduced protein level in the adult stage in comparison to the control. Thyroxine with a dose of 0.25, 0.5 and 1 μg/g increased the fat body RNA content over the control level which was observed on days 2, 4 and 8. But on day 13, the RNA content in these groups returned to the control level. Higher doses of T4 (2 and 5 μg/g) decreased the RNA content during the developmental period. DNA content was not altered by lower doses of T4 (0.25,0.5 and 1 μg/g), while the higher doses (2 and 5 μg/g) surprisingly caused a reduction in DNA content during the larval, pupal and adult stages.

The increase in protein and RNA contents with lower doses of T4 and decrease with higher doses, indicates a biphasic nature of thyroid hormone action in silkworm fat body.

Polyacrylamide disc gel electrophoresis (PAGE) was performed on soluble proteins from the fat body, haemolymph (male and female), and ovary of the adult fresh water-bug, Laccotrephes rubra, in order to determine their protein patterns. The electrophoresis resulted in the separation of 16 and 17 protein components in male and female haemolymph respectively. In female fat body extracts 15 protein bands could be detected; whereas ovary extracts resolved into 11 protein bands only. Comparison of the electropherograms of protein pattern of fat body (FBPP), haemolymph (HPP) and ovary (OPP) revealed that the extra band present in the female haemolymph is common to both female fat body and ovary, which is suggestive of it being the female specific protein, i.e. vitellogenin. A careful examination of the various electropherograms further revealed that the majority of the protein bands of haemolymph and ovary are common to its corresponding fat body protein bands. This might suggest that the ovary derives most of its protein components from the surrounding haemolymph, which have presumably been synthesized and secreted by the fat body.

The histochemical analyses demonstrated that the female-specific protein band is a glycolipoprotein; and most of the haemolymph protein zones stain as glycoprotein, lipoprotein or ribonucleoprotein. ‘Stains-all’ technique however, revealed the presence of four possible RNA bands in fat body extracts.

Most dissected Nezara viridula (91.6%) from night catches had their stomach filled (half-full-full) with food, and females had a higher feeding activity than males. Females outweighed males at the ratio 1.3: 1, and an individual was heavier in October than in May. Ovarian development corresponded closely with decreasing fat body of females, and immature individuals had maximum fat in the abdomen. The spent individuals with empty stomach and fat thinly spread over the venter were relatively abundant in April and May, implicating the possibility of large-scale oviposition during these seasons.