Transformation of Rana tigrina during Progressive Metamorphosis

2021 ◽  
Vol 30 (1) ◽  
pp. 102-109
Author(s):  
Dhananjay Mishra ◽  
K.Venu Achari

We determined the kinetics of metamorphosis, apoptosis, and tail regression in Rana tigrina. Acid phosphatase activity (µMole Pi.hr-1.tail-1) in the growing and regressing tail attended six to thirty fold increase respectively. However total activity in the trunk was decreased through progressive growing stages of metamorphosis. Total protein content in the trunk of tadpoles at climax stage (XXI) was decrease (35%) from 2.6mg/ml to 1.7mg/ml. The tail of tadpole tissue has shown a two fold increase in total Ribonucleic Acid (RNA) content from stage III to stage XVIII. But there was again decrease in total RNA content at climax stage (stage XXI). This might be possible due to decreased protein synthetic status. When the experiment was performed in trunk homogenate the amount of total carbohydrate (mg/ml) was slightly increased from 37mg/ml to 38.6mg/ml. this might be due to increase in the activity of α-amylase enzymes in the viscera of developing tadpole when it reached the climax stage.

Author(s):  
Yifan Gao ◽  
Jia Feng ◽  
Junping Lv ◽  
Qi Liu ◽  
Fangru Nan ◽  
...  

In order to study the effects of nitrogen stress on the lipid synthesis of Parachlorella kessleri TY02 and to understand the changes in growth, photosynthetic pigments, total protein and total carbohydrate contents during lipid accumulation, the cells of the strain were cultured in nitrogen-deficient (N−) and nitrogen-rich (N+) media for one week. Changes in cell growth, chlorophyll content, chlorophyll fluorescence parameters, neutral lipid and total lipid content, total protein content and total carbohydrate content were measured and analyzed. The results showed that, under nitrogen stress, the algal strain grew slowly, and chlorophyll and total protein contents decreased, while total carbohydrate and total lipid contents increased. This indicated that, under nitrogen stress, most of the carbon flowed to the synthesis of lipids and carbohydrates. Meanwhile, reducing the nitrogen content was a relatively economical and easy to operate method of promoting lipid accumulation.


Weed Science ◽  
1978 ◽  
Vol 26 (1) ◽  
pp. 90-93 ◽  
Author(s):  
P. K. Biswas ◽  
A. Devi ◽  
P. K. Roy ◽  
K. B. Paul

In order to germinate successfully, large crabgrass [Digitaria sanguinalis(L.) Scop.] seeds require a period of after-ripening. Some changes, either physical, biochemical or both, must occur in these seeds during this after-ripening process. This paper reports the differences in the activities of several enzymes between dormant (non-after-ripened) and nondormant (after-ripened) large crabgrass seeds at various periods of hydration. The total protein content of dormant seeds does not change during imbibition but increases greatly in nondormant seeds at 48 and 76 h of hydration. Initially, nondormant seeds exhibit high alpha-amylase activity and low peroxidase and acid phosphatase activities. Alpha-amylase activity remains unchanged relatively in both dormant and nondormant seeds up to 36 h of hydration, but increases greatly in nondormant seeds at 48 and 76 h of hydration. Peroxidase activity, which is initially low in nondormant seeds, increases substantially at 48 and 76 h of soaking. Acid phosphatase activity in dormant seeds does not change following hydration but is gradually elevated in nondormant seeds with duration of soaking. Lipase activity in dormant seeds remains fairly constant upon hydration. In nondormant seeds, however, the activity gradually decreases with duration of soaking, the decrease being 3 to 4 fold at 76 h of imbibition. Except for lipase, there is a positive correlation in the activities of alpha-amylase, peroxidase, and acid phosphatases with the increase of total protein content of nondormant seeds.


1990 ◽  
Vol 17 (4) ◽  
pp. 401-406
Author(s):  
Isabella Mazziotti ◽  
Anna-Laura Stammati ◽  
Flavia Zucco

Twenty-six chemicals supplied coded by FRAME, were tested on HEp-2 cells. Three endpoints were used to measure the cytotoxicity of these compounds: total protein content, LDH release and total acid phosphatase content. The sensitivity of these parameters is discussed. The results are compared with those obtained by other groups participating in the validation scheme organised by FRAME.


Metabolites ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 268
Author(s):  
Kosuke Saito ◽  
Kotaro Hattori ◽  
Shinsuke Hidese ◽  
Daimei Sasayama ◽  
Tomoko Miyakawa ◽  
...  

Lipidomics provides an overview of lipid profiles in biological systems. Although blood is commonly used for lipid profiling, cerebrospinal fluid (CSF) is more suitable for exploring lipid homeostasis in brain diseases. However, whether an individual’s background affects the CSF lipid profile remains unclear, and the association between CSF and plasma lipid profiles in heathy individuals has not yet been defined. Herein, lipidomics approaches were employed to analyze CSF and plasma samples obtained from 114 healthy Japanese subjects. Results showed that the global lipid profiles differed significantly between CSF and plasma, with only 13 of 114 lipids found to be significantly correlated between the two matrices. Additionally, the CSF total protein content was the primary factor associated with CSF lipids. In the CSF, the levels of major lipids, namely, phosphatidylcholines, sphingomyelins, and cholesterolesters, correlated with CSF total protein levels. These findings indicate that CSF lipidomics can be applied to explore changes in lipid homeostasis in patients with brain diseases.


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.


2005 ◽  
Vol 33 (3) ◽  
pp. 207-213 ◽  
Author(s):  
Paul J. Dierickx

In our previously described Hep G2/24-hour/total protein assay, protein levels were measured by using the Lowry method. This assay was the best acute in vitro assay for the prediction of human toxicity within the Multicentre Evaluation of In Vitro Cytotoxicity (MEIC) study. In order to increase the MEIC data-base with a wider range of chemicals, we were interested in introducing the more practical 3-(4-carboxybenzoyl)-quinoline-2-carboxaldehyde (CBQCA) method for the quantification of the total protein content. Therefore, we investigated whether the same good results for the prediction of acute human toxicity would be obtained with the CBQCA method. The cells were treated for 24 hours, then cytotoxicity was determined by measuring the total protein content with CBQCA. The results were quantified by using the PI50c: the concentration (in mM) of test compound required to reduce the total protein content measured with the CBQCA-method by 50% as compared to the control cells. The results were compared with the PI50, the corresponding value when the Lowry method was used. A relatively low correlation was observed between PI50 and PI50c, reflecting the large and unexpected, differences when using the two protein assays. However, when comparing the log PI50c with the human toxicity, a correlation coefficient of r2 = 0.761 ( n = 44) was obtained for exactly the same series of MEIC chemicals. This value is clearly higher than that for the Lowry method ( r2 = 0.695). Compared to the Lowry method originally used, the Hep G2/24-hour/CBQCA total protein assay has the additional important advantage that it can be very easily adapted for large-scale analyses with robotic systems, including the on-line calculation of the results.


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