Polyclonal antibodies against PBAN were used to map the distribution of PBAN-like antigenic sites in the brain-suboesophageal ganglion (Br-SOG) complex, associated neurohaemal structures, ventral nerve cord ganglia and in the alimentary canal. A pair of lateral neurosecretory cells immunopositive to the antiserum were found in each half of the deutocerebrum. PBAN-like immunoreactivity (PLI) was also noticed in the tritocerebral region of the brain and in the aorta. Two groups of immunopositive cells of four and two cells respectively, were found in the SOG. Small and weakly immunoreactive neurons were identified in the prothoracic ganglion, whereas in the pterothoracic ganglion a pair of cells reacted positively to the antibody. Immunoreactive cells were also identified in the corpora cardiaca. Some of the epithelial endocrine cells of the midgut also showed immunoreactivity to PBAN antiserum.
The aim of this study was to show that the kind of AKH-mobilized energy substrates in insects can be predicted on the basis of the results obtained with the application of heterologous, i.e. inter-species, AKHs. Four different AKHs, the Locmi-AKH-I inducing hyperlipaemia and hyperglycaemia in Locusta migratoria, Tenmo-HrTH inducing hyperglycaemia in Tenebrio molitor, and Pyrap-AKH and Peram-CAH-II inducing hyperlipaemia in Pyrrhocoris apterus were used, firstly in conspecific tests, secondly in all possible species-AKH combinations, and finally in individual applications on the test species, the cotton bug Dysdercus cingulatus. Since each of the AKHs induced hyperlipaemia in D. cingulatus adults, we predicted that lipids are the only energy substrates which are mobilized in this species by its native AKH. The accuracy of this prediction was subsequently confirmed by the structural identification of the native D. cingulatus AKH and conspecific application tests. The proposed methodical approach can serve as a suitable monitoring system for determination of the kind of energy substrates mobilized by native insect AKHs until the structure of the hormone is identified.