Role of hepcidin in murine brain iron metabolism

Brain iron homeostasis is maintained by a balance of both iron uptake and release, and accumulating evidence has revealed that brain iron concentrations increase with aging. Hepcidin, an iron regulatory hormone produced by hepatocytes in response to inflammatory stimuli, iron, and hypoxia, has been shown to be the long-sought hormone responsible for the regulation of body iron balance and recycling in mammals. In this study, we report that hepcidin is widely expressed in the murine brain. In cerebral cortex, hippocampus and striatum, hepcidin mRNA levels increased with aging. Injection of hepcidin into the lateral cerebral ventricle resulted in decreased Fpn1 protein levels in cerebral cortex, hippocampus, and striatum. Additionally, treatment of primary cultured neurons with hepcidin caused decreased neuronal iron release and Fpn1 protein levels. Together, our data provide further evidence that hepcidin may be involved in the regulation of brain iron metabolism.     

Presence of serum proteins in submaxillary duct perfusate

The secretory activity of the main excretory duct of rat submaxillary gland was investigated by the technique of luminal perfusion. Immunologic studies of the perfusate revealed the presence of serum antigens and the absence of intrinsic submaxillary gland antigens. It is suggested that the submaxillary duct permits passive transport of serum proteins to saliva from serum.     

Presence of serum proteins in submaxillary duct perfusate

Summary The secretory activity of the main excretory duct of rat submaxillary gland was investigated by the technique of luminal perfusion. Immunologic studies of the perfusate revealed the presence of serum antigens and the absence of intrinsic submaxillary gland antigens. It is suggested that the submaxillary duct permits passive transport of serum proteins to saliva from serum.     

Role of salivary glands in the maintenance of midgut amylase activity inPeriplaneta americana L.

Summary It was experimentally demonstrated, by the surgical removal of salivary glands and severence of salivary ducts, that most of the amylase in the gut ofPeriplaneta americana comes from the salivary glands.We wish to acknowledge Prof. H. Swarup (Jiwaji University, Gwalior, M.P.) for working facilities provided at School of Studies in Zoology, Vikram University, Ujjain, M.P., and Council of Scientific and Industrial Research, New Delhi, for fincancial support in the form of Junior Research Fellowship to one of us (O.P.A.)     

Role of the nerve cord in the control of prothoracic glands inGalleria mellonella L.

Summary Certain lesions of the nerve cord in postfeeding larvae impede pupation by altering the proprioreceptive input, which modulates the prothoracicotropic activity of the brain. Direct influence of ventral ganglia on prothoracic glands is negligible.     

Denervation and reinnervation of the rat's submaxillary gland

Zusammenfassung Parasympathische chirurgische Denervierung der Submaxillarisdrüse der Ratte führt zu einer Sensibilisierung der Effektorzellen, einer reduzierten Gesamtaktivität der Cholin-Acetyltransferase innerhalb von 1–2 Tagen und zu einer Gewichtsabnahme der Drüsen innerhalb von 4 Tagen. Das erste Zeichen einer Reinnervation ist eine verminderte Sensibilisierung und eine gesteigerte Enzymaktivität nach etwa 2 Monaten; das Gewicht der denervierten Drüsen nimmt nach 5 Monaten zu. Die Reinnervation ist nach 10 Monaten noch nicht vollständig.     

Role of adenosine A1 and A2 receptors in the regulation of aldosterone production in rat adrenal glands

To investigate the roles of adenosine A1 and A2 receptors in the regulation of aldosterone production, we examined the effects of adenosine and adenosine agonists (N6-cyclohexyl adenosine; selective adenosine A1 receptor agonist and 5'-N-ethylcarboxamine adenosine; selective adenosine A2 receptor agonist) on aldosterone and cyclic AMP production in rat adrenal capsular cells. Neither adenosine nor 5'-N-ethylcarboxamine adenosine caused significant effects on basal aldosterone or cyclic AMP production. Also, adenosine (10(-3) M) showed no consistent effects on aldosterone and cyclic AMP production induced by ACTH. On the other hand, N6-cyclohexyl adenosine exhibited a significant inhibition of basal aldosterone and cyclic AMP production at doses of 10(-4) M and 10(-3) M; furthermore, 10(-3) M N6-cyclohexyl adenosine inhibited aldosterone and cyclic AMP production stimulated by ACTH. These results suggest that adenosine A1 receptors are coupled to and inhibit adenylate cyclase and may be involved in the inhibition of aldosterone production.     

Role of adenosine A1 and A2 receptors in the regulation of aldosterone production in rat adrenal glands

Summary To investigate the roles of adenosine A₁ and A₂ receptors in the regulation of aldosterone production, we examined the effects of adenosine and adenosine agonists (N⁶-cyclohexyl adenosine; selective adenosine A₁ receptor agonist and 5-N-ethylcarboxamine adenosine; selective adenosine A₂ receptor agonist) on aldosterone and cyclic AMP production in rat adrenal capsular cells. Neither adenosine nor 5-N-ethylcarboxamine adenosine caused significant effects on basal aldosterone or cyclic AMP production. Also, adenosine (10^–3M) showed no consistent effects on aldosterone and cyclic AMP production induced by ACTH. On the other hand, N⁶-cyclohexyl adenosine exhibited a significant inhibition of basal aldosterone and cyclic AMP production at doses of 10^–4 M and 10^–3 M; furthermore, 10^–3 M N⁶-cyclohexyl adenosine inhibited aldosterone and cyclic AMP production stimulated by ACTH. These results suggest that adenosine A₁ receptors are coupled to and inhibit adenylate cyclase and may be involved in the inhibition of aldosterone production.