Anthocyanin Influence on Water Proton NMR Relaxation Times and Water Contents in Leaves of Evergreen Woody Plants During the Winter

An investigation was made to determine the effect of anthocyaninin red-colored evergreen leaves during the mid-winter on waterproton NMR relaxation times (T₁). Water contents, anthocyanincontentsand histologic localization of red-coloration in mesophyllswere determined by using both red-colored and green leaves fromthe same branches of Rhododendron, Viburnum and Mahonia, respectively.Although the decrease of water contents in the red-colored leavesin Mahonia was insignificant, decreases in the former two specieswere clearly observable. T₁ differences between red-coloredand green leaves for the three species were insignificant. Increasesof anthocyanin contents and histologic localization of red colorationin mesophylls for the red-colored leaves were more pronouncedin Rhododendron and Viburnum than in Mahonia. These observationssuggest that the pronounced increases of histologic localizationof red-colored mesophyll cells and anthocyanin contents in red-coloredleaves for the former two species contribute to maintenanceof T₁ relaxation times in spite of the marked decrease of watercontents in leaves. It is assumed that the increase of localizationareas of red-colored parenchymatous cells in mesophylls is moreeffective than the total contents of anthocyanins in leavestowards the maintenance of the T₁ level in red-colored leaves,and this appears to be dependent on the vacuolar compartmentationof anthocyanin in mesophyll cells. (Received August 3, 1991; Accepted December 12, 1991)     

Expression of neuron-specific enolase in the pineal organ of the domestic fowl during post-hatching development

Immunohistochemistry for neuron-specific enolase (NSE) revealed that NSE is localized in both a limited number of pinealocytes and intrinsic afferent neurons in the pineal organ of the domestic fowl. Furthermore, a computer-assisted three-dimensional imaging technique allowed to clarify the reverse distributional pattern of both elements: NSE-positive pinealocytes displayed a dense distribution especially in the vesicular portion of the gland, whereas NSE-immunoreactive nerve cells were mainly found in the pineal stalk. The number of NSE-positive intrinsic neurons in the pineal organ of chickens decreased rapidly after hatching, with a concentration of these elements in the basal portion (stalk) of the pineal organ. On the other hand, immunoreactive pinealocytes increased remarkably in the end-vesicle of the organ with age, followed by a gradual expansion toward the proximal portion. Thus, the spectacular increase in NSE-positive pinealocytes and the progressive reduction of reactive neurons occurred in parallel during the course of post-hatching development. NSE-immunoreactive pinealocytes displayed morphological characteristics of bipolar elements, endowed with an apical protrusion into the pineal lumen and a short basal process at younger stages, whereas multipolar types of NSE-positive pinealocytes were predominantly found in the adult domestic fowl. These results indicate that in the pineal organ of the domestic fowl (1) the ontogenetic expansion of NSE-immunoreactive pinealocytes is paralleled by a regressive afferent innervation, (2) the NSE-positive pinealocytes transform from a bipolar (columnar) type to a multipolar type during post-hatching development, and (3) these ontogenetic changes in the NSE-immunoreactivity and morphology of pinealocytes may reflect the development of a neurosecretory-like capacity of the organ.     

Role of increase in intracellular calcium in PTH-induced homologous desensitization in UMR-106 cells.

Effects of increase in intracellular calcium on PTH-induced homologous desensitization were investigated using calcium ionophores. Pretreatment of UMR-106 cells (rat osteoblast like osteosarcoma cell line) with calcium ionophores (A23187 or ionomycin) for 6h resulted in approximately 50% decrease of PTH-stimulated cAMP production. PTH receptor binding, assessed with 125I-[Nle8,Nle18,Tyr34]PTH-(1-34) as radioligand, was significantly decreased in 10(-6) M calcium ionophore-pretreated (for 6h) cells without affecting the dissociation constant (Kd) for PTH. Minimal effective treatment period was 2h and similar inhibitory effect was observed in 12h-treated cells. These data suggest that increase in intracellular calcium might also act on PTH receptor in the similar manner as protein kinase C activation to induce desensitization.