CALCIUM BALANCE AND MOULTING IN THE CRUSTACEA

1. Crustaceans have a high content of calcium, which is chiefly located in the skeleton as calcium carbonate. Calcium is generally the most abundant cation in the body. 2. During intermoult, the exoskeleton is usually fully calcified and the animal is in calcium equilibrium with its environment. 3. In the premoult stages calcium is resorbed from the skeleton and may be lost to the environment or stored within the body. Typically, losses are high and storage is small in aquatic species, whilst most terrestrial forms store much larger amounts of calcium and losses are reduced. Loss of calcium in soluble form by aquatic species must be by outward transport across the gills. 4. Calcium is stored in a variety of different ways, usually with a common taxonomic theme. The main forms are as calcium phosphate granules in cells of the midgut gland (Brachyura), gastroliths (Astacidea and some Brachyura), the haemocoel (some Brachyura) the posterior midgut caeca (Amphipoda) and the ventral portion of the body generally in the Isopoda. 5. At ecdysis, the skeleton is shed and the calcium remaining in it is lost from the body. 6. Recalcification begins immediately, or shortly after, ecdysis using calcium mobilized from the stores. Simultaneously, or when the stores are exhausted, other sources of calcium are utilized. These are calcium in the water (aquatic species), the food (aquatic and terrestrial species) and the exuviae (chiefly terrestrial species). 7. Marine species store little calcium and must obtain the bulk of their requirement (ca. 95%) from the water. Fresh-water species also store little calcium but have, seemingly, adapted to the lower availability of calcium by increasing the affinity of the calcium-absorbing mechanism. The rates of uptake of calcium are consequently similar in marine and fresh-water species. 8. A high degree of storage is essential for terrestrial crustaceans as they do not have access to a large aquatic reservoir of calcium. These large reserves enable the animals to reach an advanced stage of calcification, allowing the resumption of foraging and feeding necessary for completion of calcification. 9. The control of calcium metabolism during the intermoult cycle is poorly under stood. β Ecdysone appears to control the resorption of calcium and the formation of calcium stores during premoult, but the mechanism of control of calcium metabolism during postmoult and intermoult is unknown. 10. The concentration of calcium in the haemolymph of most species is high, but a large proportion of this is in non-ionized form. In premoult, total calcium levels rise as a result of calcium resorption but little change occurs in the concentration of ionized calcium. Postmoult generally sees a fall in blood calcium, sometimes below the intermoult value.     

内分泌细胞中溶酶体对激素分泌调节的作用

本实验用外源性雄激素引起垂体促性腺激素细胞和睾丸间质细胞分泌抑制,对这两种细胞中的溶酶体及分泌吞噬和自体吞噬活动进行了超微结构形态观察和半定量分析。实验中应用了CMP酶细胞化学技术和免疫胶体金技术。研究结果显示,在分泌受抑制状态下,垂体促性腺激素细胞中溶酶体增多,分泌吞噬活动加强;与此同时,睾丸间质细胞也表现溶酶体增多、自体吞噬活动加强。这些结果不仅再次证明在分泌蛋白质激素细胞中溶酶体以分泌吞噬的方式参与了激素分泌调节,更重要的是初步证明在分泌类固醇激素细胞的分泌调节中,也有溶酶体的参与,其形式是自体吞噬作用。细胞通过自体吞噬作用得以在短时间内清除一部分合成激素的细胞器和其中的激素,这可能是分泌类固醇激素的细胞及时有效地调整激素分泌量的一项重要机制,与分泌蛋白质激素细胞的分泌吞噬有着相同的意义。     

大熊猫胃肠道内分泌细胞分布型的研究

本文用ＰＡＰ法对３只大熊猫胃底,幽门腺区、十二脂肠,空肠,回肠、结肠和直肠的五羟色胺,生长抑素,胃素,胆囊收缩囊,神经降压素、胃动素、抑胃多肽、胰高血糖素、血管活性肠肽和内啡肽的ＩＲ细胞进行了研究。结果表明,大熊猫胃肠道粘膜上皮中具有前八种ＩＲ细胞。对７年龄个体胃肠各段相对数量的比较和各段内分布情况的观察结果表明,除五羟色胺ＩＲ细胞在空肠分布较多外,大多数种类的ＩＲ细胞集中分布于幽门区和十二指肠,     

鱼类胃肠胰内分泌系统APUD细胞研究的现状

免疫细胞化学(Immunocyto chemistry)又称为免疫组织化学(Immunohisto chemistry),是近年发展起来的一门新的边缘学科.       

CILIA AND VESICULAR PARTICLES IN THE ENDOCRINE PANCREAS OF THE MONGOLIAN GERBIL

Though the general appearance and the cellular composition of the pancreatic islets of the Mongolian gerbil (Meriones unguiculatus) conformed to those of most other rodent species, some peculiar ultrastructural details were found. Thus there were diversiform, mainly vesicular particles with varying electron opacity in these islets. The vesicular particles showed a clear association to cilia which seemed to possess a basic fiber pattern of 9 + 0. The basal bodies were localized in the cytoplasm of the islet parenchymal cells, most often in the β-cells, and the vesicular particles occurred in the portions of cilia that were protruding into intercellular spaces. The cilia were often swollen, and the vesicular particles were mainly found in the space between the ciliary membranes and the longitudinal fibers. A few vesicular particles could be seen inside and sometimes seemingly in contact with these fibers. Occasionally, there were morphologically similar structures in the cytoplasm of adjacent β-cells. The vesicular particles were differentiated from the vesicles occurring in nerve structures by their larger size, as well as by their heterogeneous shape and electron opacity. The nature of the vesicular particles and the significance of their presence in cilia and in the cytoplasm of some of the islet cells remain unknown. Among other possibilities, it is, however, suggested that the vesicular particles may represent secretory material.     

THE ENDOCRINE BASIS OF PAIR-FORMATION BEHAVIOUR IN THE MALE EIDER SOMATERIA MOLLISSIMA

Pair-formation behaviour among the Eiders began after the annual moult, in late September. There was a small peak of display in October and November and a large one in the following April and May. As a result, the female population became paired in two phases, up to 50% in the autumn and the remainder in the following spring. The seasonal cycle of the abundance of Leydig cells was bimodal, with a peak in October and a large one in April-May. That the peaks represent increased androgen production was supported by the cycles of Leydig cell enzyme activity and lipid content and of penis weight. The monthly means of Leydig cell abundance and of the rate of display were statistically correlated. Experiments with sexually quiescent males in eclipse plumage demonstrated that testosterone was capable of inducing pair-formation behaviour. Relatively advanced stages of spermatogenesis were found in autumn, and were maintained through the winter, complete development occurring in the spring. Seasonal changes in the production of pituitary gonadotropin followed a bimodal pattern with peaks in autumn and in the spring. Field evidence is presented which suggests that Follicle Stimulating Hormone and Luteinizing Hormone were produced at different phases of a circadian rhythm of photosensitivity.