Localization of substance P in the nervous system of the human fetus : preliminary results

Substance P (SP) immunoreactive structures were localized by immunofluorescence technique within the central nervous system of human fetuses (12, 15, 19 and 24 weeks old). Specificity of the anti-SP serum was established by immunocytology and radio-immunology. A wide distribution of SP positive structures (pericaryons and/or fibres) was found in brain, spinal cord and dorsal root ganglia. Mesencephalon, pons and dorsal horns of the spinal cord showed very intense fluorescence. The preliminary observations are the first report concerning SP ontogeny in the Human central nervous system. However, it was difficult to ascribe a significance to this neuropeptide during fetal life.     

Toxicity of some insecticides for crowded and isolated nymphs ofGryllodes sigillatus Wlk. (Orthoptera: Gryllidae)

Summary 6 insecticides; chlordane, malathion, fenitrothion, pyrethrum, rotenone and sevin, were screened againstGryllodes sigillatus Wlk. reared under crowded and isolated conditions. Chlordane was found to be most toxic, followed by malation, fenitrothion, pyrethrum, rotenone and sevin. Insects reared under crowded conditions were more susceptible to insecticides than insects reared under isolated conditions.Acknowledgments. The authors are grateful to Dr S. C. Saxena for providing all facilities.     

Pharmacological studies of a new analgesic,dl-erythro-1-phenyl-2-(o-chlorophenyl)-2-[4-(p-methoxybenzyl)-1-piperazinyl] ethanol dihydrochloride,in experimental animals

Summary dl-Erythro-1-phenyl-2-(o-chlorophenyl)-2-[4-(p-methoxybenzyl)-1-piperazinyl] ethanol dihydrochloride showed orally a definite analgesic activity, without producing the significant morphine-like physical dependence liability, and its analgesic potency was about a half that of codeine and far superior to aminopyrine in experimental animals.     

Ankyrin and spectrin associate with voltage-dependent sodium channels in brain

The segregation of voltage-dependent sodium channels to specialized regions of the neuron is crucial for propagation of an action potential. Studies of their lateral mobility indicate that sodium channels are freely mobile on the neuronal cell body but are immobile at the axon hillock, presynaptic terminal and at focal points along the axon. To elucidate the mechanisms that regulate sodium channel topography and mobility, we searched for specific proteins from the brain that associate with sodium channels. Here we show that sodium channels labelled with 3H-saxitoxin (STX) are precipitated in the presence of exogenous brain ankyrin by anti-ankyrin antibodies and that 125I-labelled ankyrin binds with high affinity to sodium channels reconstituted into lipid vesicles. The cytoplasmic domain of the erythrocyte anion transporter competes for the latter interaction. Neither the neuronal GABA (gamma-aminobutyric acid) receptor channel complex nor the dihydropyridine (DHP) receptor bind brain ankyrin. The results indicate that brain ankyrin links the voltage-dependent sodium channel to the underlying cytoskeleton and may help to maintain axolemmal membrane heterogeneity and control sodium channel mobility.