Synthesis of a haemolymph hexamerin by the fat body and testis of Rhodnius prolixus

1994 ◽  
Vol 24 (1) ◽  
pp. 59-67 ◽  
Author(s):  
F.S. Faria ◽  
E.S. Garcia ◽  
S. Goldenberg
Keyword(s):  
Fat Body ◽  
1965 ◽  
Vol 43 (3) ◽  
pp. 425-431
Author(s):  
G. C. COLES

1. There are two adult-specific proteins in the haemolymph of Rhodnius. They appear to be formed in the fat body. 2. The two proteins are absorbed by the oocytes and form the bulk of the soluble egg proteins. 3. The changes in the concentration of total protein in the haemolymph and of four protein fractions, as separated on cellulose acetate, do not reflect egg production. This may be a consequence of the hormonal control of reproduction.


1952 ◽  
Vol 29 (4) ◽  
pp. 561-570
Author(s):  
V. B. WIGGLESWORTH

The ‘moulting hormone’ in Rhodnius is composite. The factor secreted in the dorsum of the brain activates a gland in the thorax which then produces the factor initiating growth and moulting. Implantation of the thoracic gland will induce moulting in the isolated abdomen; implantation of the brain is effective only if the thorax is intact. This system agrees with that described in Lepidoptera and Diptera and is probably widespread in insects. The thoracic gland in Rhodnius consists of a loose network of very large cells, richly supplied with tracheae, spread as a single diffuse layer over the surface of the inner lobes of the thoracic fat-body. These cells go through a cycle of secretory activity which reaches its peak during the critical period. They break down and disappear within 2 days after the insect becomes adult. The adult Rhodnius is caused to moult by implantation of the thoracic gland from a moulting larva; it is not caused to moult by implantation of the brain.


1970 ◽  
Vol 48 (3) ◽  
pp. 489-493
Author(s):  
B. H. Millen ◽  
W. E. Beckel

Fourth-instar nymphs of Rhodnius prolixus were starved for 23 weeks and then gorged on nutrient (blood) or non-nutrient (saline with dextran) diet. Light microscopy was used to examine changes occurring in the nuclei and nucleoli of the fat body cells for 5 days after feeding.In starved nymphs, all features of the nuclei and nucleoli indicate functional inactivity. Two types of chromatin granules can be distinguished. In a given nucleus, one type appears to be exclusive.Blood feeding causes changes in the nuclei and nucleoli manifesting cell activation, i.e. restoration of the cell's capacity for protein synthesis. The activation criteria noted were: enlargement of the nuclei and nucleoli; accumulation of ribonucleic acid (RNA) by the nucleoli; alteration of chromatin granule structure; dispersion of Fused chromatin granules from about the nucleoli; elaboration of the intra-nucleolar chromatin within the nucleolus; and contortion of the shape of the nucleolus.Saline with dextran feeding does not cause cell activation. Instead, the cells undergo accelerated wastage as reflected by degenerative changes in the nuclei (pyknosis) and nucleoli.


2002 ◽  
Vol 32 (11) ◽  
pp. 1409-1417 ◽  
Author(s):  
Emerson G Pontes ◽  
Luciano A.M Grillo ◽  
Katia C Gondim
Keyword(s):  
Fat Body ◽  

2021 ◽  
Vol 12 ◽  
Author(s):  
Petter F. Entringer ◽  
David Majerowicz ◽  
Katia C. Gondim

Insects are unable to synthesize cholesterol and depend on the presence of sterols in the diet for cell membrane composition and hormone production. Thus, cholesterol absorption, transport, and metabolism are potential targets for vector and pest control strategies. Here, we investigate the dietary cholesterol absorption and tissue distribution in the kissing bug Rhodnius prolixus using radiolabeled cholesterol. Both the anterior and posterior midguts absorbed cholesterol from the ingested blood, although the anterior midgut absorbed more. We also observed esterified cholesterol labeling in the epithelium, indicating that midgut cells can metabolize and store cholesterol. Only a small amount of labeled cholesterol was found in the hemolymph, where it was mainly in the free form and associated with lipophorin (Lp). The fat body transiently accumulated cholesterol, showing a labeled cholesterol peak on the fifth day after the blood meal. The ovaries also incorporated cholesterol, but cumulatively. The insects did not absorb almost half of the ingested labeled cholesterol, and radioactivity was present in the feces. After injection of 3H-cholesterol-labeled Lp into females, a half-life of 5.5 ± 0.7 h in the hemolymph was determined. Both the fat body and ovaries incorporated Lp-associated cholesterol, which was inhibited at low temperature, indicating the participation of active cholesterol transport. These results help describe an unexplored part of R. prolixus lipid metabolism.


2007 ◽  
Vol 79 (1) ◽  
pp. 53-62 ◽  
Author(s):  
Gutemberg G. Alves ◽  
Monica M. Marinho-Carvalho ◽  
Georgia C. Atella ◽  
Mario A.C. Silva-Neto ◽  
Mauro Sola-Penna

6-phosphofructo-1-kinase (phosphofructokinase; PFK) activity from Rhodnius prolixus, a haematophagous insect which is usually a poor flyer, was measured and compared in two metabolically active tissues - flight muscle and fat body. The activity of this important regulatory glycolytic enzyme was much more pronounced in muscle (15.1 ± 1.4 U/mg) than in fat body extracts (3.6±0.4 U/mg), although the latter presented higher levels of enzyme per protein content, as measured by western-blotting. Muscle extracts are more responsible than fat body to ATP and fructose 6-phosphate, both substrates of PFK. Allosteric regulation exerted by different effectors such as ADP, AMP and fructose 2,6-phosphate presented a singular pattern for each tissue. Optimal pH (8.0-8.5) and sensitivity to pH variation was very similar, and citrate was unable to inhibit PFK activity in both extracts. Our results suggest the existence of a particular PFK activity for each tissue, with regulatory patterns that are consistent with their physiological roles.


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