scholarly journals Ontogenetic changes in DNA and RNA content of laboratory-reared Prochilodus lineatus larvae: use of RNA/DNA ratios as indicators of nutritional condition

2018 ◽  
Vol 69 (3) ◽  
pp. 455 ◽  
Author(s):  
M. V. Diaz ◽  
M. I. Gómez ◽  
S. Sánchez ◽  
C. M. Fuentes

The aims of the present study were to describe the ontogenetic performance of DNA and RNA content, as well as to assess the nutritional condition of Prochilodus lineatus larvae reared under different feeding treatments. The experiment consisted of two parts, the first 6–14 days after hatching (DAH) and the second 15–21 DAH. In the first part of the experiment, larvae were kept under one of two feeding treatments: fed or starved. During the second part of the experiment, larvae were kept under one of four treatments: fed, fed until 14 DAH and later starved, starved until 14 DAH and fed later or starved. It is of note that the size and weight reached of larvae that were starved during early development and later received food were higher than those of than larvae in the other feeding treatments. In addition, instantaneous growth rates were higher and nutritional condition was better in larvae that were initially starved and fed later. The availability of food following a period of starvation seems to trigger larval metabolism and cellular division. Consequently, we recommend maintaining appropriate food provision in the aquaculture of P. lineatus larvae, especially in advanced developmental stages. We verified that RNA/DNA ratio is affected by the feeding condition and that it is sensitive enough to promptly reflect changes in feeding conditions of P. lineatus larvae. Thus, the RNA/DNA ratio could be used to assess nutritional condition of both wild and cultured P. lineatus larvae.

1970 ◽  
Vol 68 (10) ◽  
pp. 331-359 ◽  
Author(s):  
W. C. O. Hill ◽  
W. B. Spatz

SynopsisDescriptions are offered of two foetal gorillas representative of developmental stages intermediate between those previously described by Duckworth (1904), Schultz (1927) and Deniker (1885). They are numbered accordingly II and IV and comparison made throughout with the other stages represented in the literature.Special attention has been paid to the ontogenetic changes occurring in the bodily form, and posture, cutaneous structures, cranial and skeletal development and in the disposition of the thoracic and abdominal viscera, much of which is previously known only in respect of Deniker's stage V.


1973 ◽  
Vol 74 (1_Suppl) ◽  
pp. S9-S69 ◽  
Author(s):  
Evangelos A. Petropoulos

ABSTRACT Interrelations among maternal, fetal and placental endocrine systems have received little attention in the extensive studies thus far conducted on placental endocrine function. Yet, increasing indirect evidence suggests that maternal and fetal endocrine glands affect the growth and endocrine function of the placenta. The present research was designed to investigate these interactions following the pattern of classical endocrinological experiment in which the placenta would represent the "target" gland and the maternal and fetal glands, the "tropic" glands. The maternal glands were represented by the ovaries and the adrenals, whereas the fetal glands, for practical purposes, were considered as a whole, i.e. as a present or absent fetus. All "endocrinectomies" (ovariectomy, adrenalectomy and fetectomy) were performed alone and in combination in pregnant Long - Evans rats on day 13 of gestation, and in each case the placenta was left in situ, undisturbed. Animals were divided into eight groups (4 animals in each group and for each placental age studied) as follows: normal; fetectomized (F); ovariectomized (Ō); adrenalectomized (A); fetectomized and ovariectomized (FO); fetectomized and adrenalectomized (F̄Ā); ovariectomized and adrenalectomized (ŌĀ); fetectomized, ovariectomized and adrenalectomized (F̄ŌĀ). Placentae were subsequently removed on days 15, 17, 19 and 21 of "gestation" and their growth and metabolic activity was assessed in terms of wet weight, total protein, DNA and RNA content, 3H-Leucine incorporation rate into proteins, and 59Fe-labelled blood uptake, as well as by histological techniques. Statistical analyses consisted of (1) a factorial design analysis to reveal interactions among the various factors, and (2) a t- test analysis of the differences among the simple factorial effects. Because of the similarity of placental response to F̄ and F̄Ā, Ō and OA, and FO and FOA, the following discussion is limited to groups F, Ō, F̄Ō and Ā. The histological, biochemical and functional evidence indicates that fetectomy destroys the nonendocrine elements of the rat placenta, but that the structural integrity and metabolic activity of the endocrine elements are maintained throughout "gestation". The giant and small cytotrophoblastic cells and the labyrinthine syncytiotrophoblast—elements implicated by others in the production of placental hormones—were found histologically to be sound, whereas the fetal mesenchyme and endothelium, the trophoblastic cells of the trilaminar structure connected with the fetal vessels, and the glycogen cells were found to be degenerated. The decrease observed in placental weight, total protein and RNA content throughout pregnancy, as well as the initial decrease in total DNA content are attributed to the destruction of the nonendocrine placental elements. On the other hand, the finding that placental weight, although lower than normal, remained constant throughout term, together with the findings that 3H-Leucine incorporation rate was similar to normal and total DNA content returned to control values by day 21, further indicate that some placental elements remain viable following fetectomy. Since neither 59Fe-labelled blood uptake, nor histological evidence revealed significant differences between fetectomized and control animals in the amount of maternal blood in the placenta, the biochemical changes noted above do not reflect changes in the blood content of the placentae. Ovariectomy invariably led to fetal death within 5 to 6 days. This fact was reflected in the response of all the placental parameters studied, initially displaying values similar to normal and subsequently resembling those recorded in F̄ placentae. These findings confirm the assertion by other investigators that although the ovary is essential for the maintenance of pregnancy in the rat, the functional and morphological integrity of the endocrine placental elements is not influenced by ovariectomy. The placental findings recorded in the F̄Ō group revealed a significant interaction between F̄ and Ō. Unlike F̄ and Ō animals, in F̄Ō animals placental weight, total protein, DNA and RNA content were similar to normal; 3H - Leucine incorporation rate was two to three times higher in F̄Ō and F̄ŌĀ animals than in controls. Histological examination indicated that the elements responsible for these findings were the giant cells, which increased in number and size, and the small cytotrophoblastic cells, which also proliferated; the labyrinth displayed the same picture as in F̄ animals and the amount of blood present in the placenta did not increase after F̄Ō, thus being irrelevant to the biochemical findings. It is evident that F̄ and Ō when combined, significantly stimulated the metabolic activity of the placenta. Thus the endocrine elements of the rat placenta appear to be subject of a dual inhibitory influence emanating from both the fetus and the ovary; accordingly, their removal, by eliminating the inhibitory action of fetal and ovarian factors on placental growth, leads to placental hypertrophy, whereas elimination of either one of these factors alone is not sufficient to elicit this placental response. Adrenalectomy did not affect the maintenance of pregnancy; however placental weight and total DNA and RNA content were lower than normal on day 15 of gestation whereas on day 19 total protein content was lower and 3H-Leucine incorporation rate was higher than normal. No histological changes or differences in 59Fe-labelled blood uptake were observed between placentae from Ā and normal rats. To account for these noxious effects, one might speculate that adrenalectomy disturbs the progestational and estrogenic equilibrium necessary to normal placental function. In summary, fetectomy, ovariectomy and adrenalectomy performed as single operations interfere with the growth and metabolism of the placenta but, in general, do not affect its endocrine elements. When fetectomy and ovariectomy are combined, however, these endocrine elements are released from ovarian and fetal inhibitions and proliferate, thus leading to an increase in placental weight and to biochemical changes that are generally similar to the normal changes occurring throughhout the course of gestation in the rat.


1986 ◽  
Vol 81 (1) ◽  
pp. 189-206 ◽  
Author(s):  
J. Bohrmann ◽  
A. Dorn ◽  
K. Sander ◽  
H. Gutzeit

We determined the extracellular electrical current pattern around Drosophila follicles at different developmental stages (7–14) with a vibrating probe. At most stages a characteristic pattern can be recognized: current leaves near the oocyte end of the follicle and enters at the nurse cells. Only at late vitellogenic stages was an inward-directed current located at the posterior pole of many follicles. Most striking was the observed heterogeneity both in current pattern and in current density between follicles of the same stage. Different media (changed osmolarity or pH, addition of cytoskeletal inhibitors or juvenile hormone) were tested for their effects on extrafollicular currents. The current density was consistently influenced by the osmolarity of the medium but not by the other parameters tested. Denuded nurse cells (follicular epithelium locally stripped off) show current influx, while an accidentally denuded oocyte produced no current. Our results show that individual follicles may be electrophysiologically different, though their uniform differentiation during vitellogenesis does not reflect such heterogeneity.


1975 ◽  
Vol 3 (6) ◽  
pp. 361-370 ◽  
Author(s):  
Edgard Serfling ◽  
Vladimir I. Majorov ◽  
Nikolai I. Mikichur ◽  
Taissya G. Popova ◽  
Lev S. Sandakchiev

1990 ◽  
Vol 116 (5) ◽  
pp. 507-512 ◽  
Author(s):  
W. Hiddemann ◽  
B. Wörmann ◽  
D. Messerer ◽  
R. Springefeld ◽  
Th. Büchner

1989 ◽  
Vol 63 (4) ◽  
pp. 454-483 ◽  
Author(s):  
Barry S. Kues

The benthic, free-living oyster Texigryphaea was the dominant constituent of many late Albian marine communities in the Texas and southern Western Interior regions. Large topotypic assemblages of three common lower–middle Washita Group species (T. navia and T. pitcheri in Oklahoma and T. tucumcarii in New Mexico) each display considerable morphological variation in valve shape and the proportions and expression of various features. Variation within an assemblage is partly due to ontogenetic changes but is mainly ecophenotypic, with local variation in nature of substrate, water turbulence, length of attachment time, and other factors influencing the final morphology of the mature shell. The T. navia assemblage is distinct in several important morphological characters from the other species, and the differences become more pronounced with growth. Texigryphaea navia appears to have been adapted to relatively firm substrates in moderately agitated conditions, in contrast to the other species, which occupied softer substrates in quieter environments. The essentially contemporaneous T. pitcheri and T. tucumcarii assemblages display much overlap in all measured dimensions of the left valve and in the range of intergrading morphs that compose each assemblage. Accordingly, T. tucumcarii is considered a synonym of T. pitcheri, representing populations of that species that lived in the West Texas-New Mexico area and developed only minor differences from the eastern populations. Within the T. navia topotypic assemblage are specimens intermediate between T. navia and T. pitcheri, and the eastern and western T. pitcheri assemblages contain forms apparently transitional to two other species, T. washitaensis and T. belviderensis. Ecophenotypic variation in the T. pitcheri assemblages appears to be greater than that in European Jurassic Gryphaea species and mirrors to some extent phyletic variation in European Jurassic Gryphaea lineages.


Development ◽  
1985 ◽  
Vol 85 (1) ◽  
pp. 163-175
Author(s):  
Shinobu Nakanishi ◽  
Edwin M. Uyeki

Benzamide, an inhibitor of (ADP-ribose) transferase, augmented chondrocytic differentiation of chick limb bud mesenchymal cells in micromass cultures; the incorporation of 35SO42− into the trichloroacetic-acid-insoluble constituents of cell masses as well as the formation of cartilage nodules (Nishio, Nakanishi, Doull & Uyeki, 1983) occurred about 24h earlier than in untreated cultures and continued to be enhanced in benzamide-treated cultures of stage 23- to 24-chick limb bud cells. Benzamide also significantly increased cell proliferation. However, benzamide did not affect DNA and RNA syntheses except for one period: 24 to 30 h after the start of culture, RNA synthesis was stimulated. From 48h of culture, (ADP-ribose) transferase activity decreased daily in untreated cultures, whereas benzamide treatment diminished (ADP-ribose) transferase activity 24 h earlier. On the other hand, intracellular NAD levels increased daily in untreated cultures, and benzamide significantly increased the NAD levels above untreated cultures. ATP levels did not differ significantly during the culture period, and benzamide did not affect ATP levels.


PEDIATRICS ◽  
1958 ◽  
Vol 21 (4) ◽  
pp. 581-581

In recent years the existence of a humoral factor or factors which stimulate erythropoietic activity has been demonstrated. The present paper reports further studies on the nature of this erythropoietic factor or factors. The author's studies indicate that there are at least two humoral erythropoietic facts. One is heat stable and appears to exert its effects upon cellular division of erythrocyte precursers in the marrow. The other factor is relatively thermolabile and exerts its effect through augmentation of incorporation of iron into hemoglobin. Variability in experimental results which have been reported in studies of the humoral erythropoietic factor may, in the authors' opinion, be due to differences in the material being studied (in content of these factors depending upon how the material being tested was prepared). These humoral factors are present in normal human plasma which suggests that they are involved in the maintenance of normal blood formation. Increased amounts of these factors in plasma in some anemias may be the result of local tissue hypoxia. In polycythemia vera the humoral factors may be of pathogenetic importance. The factors do not appear to be formed in hemopoietic tissue; the kidney has been suggested as a possible locus of formation.


2013 ◽  
Vol 280 (1766) ◽  
pp. 20131200 ◽  
Author(s):  
Matt Friedman ◽  
Zerina Johanson ◽  
Richard C. Harrington ◽  
Thomas J. Near ◽  
Mark R. Graham

The adhesion disc of living remoras (Echeneoidea: Echeneidae) represents one of the most remarkable structural innovations within fishes. Although homology between the spinous dorsal fin of generalized acanthomorph fishes and the remora adhesion disc is widely accepted, the sequence of evolutionary—rather than developmental—transformations leading from one to the other has remained unclear. Here, we show that the early remora † Opisthomyzon (Echeneoidea: †Opisthomyzonidae), from the early Oligocene (Rupelian) of Switzerland, is a stem-group echeneid and provides unique insights into the evolutionary assembly of the unusual body plan characteristic of all living remoras. The adhesion disc of † Opisthomyzon retains ancestral features found in the spiny dorsal fins of remora outgroups, and corroborates developmental interpretations of the homology of individual skeletal components of the disc. † Opisthomyzon indicates that the adhesion disc originated in a postcranial position, and that other specializations (including the origin of pectination, subdivision of median fin spines into paired lamellae, increase in segment count and migration to a supracranial position) took place later in the evolutionary history of remoras. This phylogenetic sequence of transformation finds some parallels in the order of ontogenetic changes to the disc documented for living remoras.


1983 ◽  
Vol 245 (1) ◽  
pp. G99-G105 ◽  
Author(s):  
T. E. Solomon ◽  
M. Vanier ◽  
J. Morisset

Pancreatic weight, [3H]-thymidine incorporation into DNA, labeling indices, and total DNA and RNA content were measured in rats treated with vehicle or 1 microgram/kg caerulein, 100 micrograms/kg secretin, or a combination of these peptides injected every 8 h for 1-5 days. Incorporation of [3H]thymidine into DNA increased 12-fold after 2 days of treatment with the combination of peptides. DNA content increased after 3 days and reached a level 1.8 times control after 5 days. Autoradiography showed that two cell types, acinar and an unidentified type, were the sites of increased DNA synthesis. Different patterns of labeling were seen in the two populations: acinar cell labeling indices were increased at 1 and 2 days (20-fold) and then fell; nonacinar cells showed an increase only after 2 days and maintained this increase after 5 days. Potentiation (greater than additive effects) was found when caerulein and secretin were injected together for all measurements except RNA content. These data indicate that DNA synthesis in two cell populations is affected by secretin and caerulein and support the occurrence of potentiation between secretin and caerulein for trophic effects on the exocrine pancreas.


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