Alterations in Carbohydrate Metabolism in Selected Tissues of Crab, Oziotelphusa Senex Senex (Fabricius) Under Fenvalerate-Induced Stress

Changes in carbohydrate metabolism in hepatopancreas and muscle of the crab, Oziotelphusa senex senex exposed to a sublethal concentration (0.2 ppm) of fenvalerate, a pyrethroid insecticide, were studied. the glycogen and total carbohydrate levels decreased significantly in the tissues of crab exposed to fenvalerate. an increase in phosphorylase 'a' and decrease in aldolase activity levels suggested increased glycogenolysis, and decreased glycolysis during fenvalerate toxicity. Krebs cycle enzymes such as NAD-isocitrate dehydrogenase, succinate dehydrogenase and malate dehydrogenase were decreased, suggesting reduced mitochondrial oxidative metabolism. Glucose-6-phosphate dehydrogenase activity was increased significantly, indicating enhanced oxidation of glucose through the hexose monophosphate shunt pathway. Lactate dehydrogenase activity was elevated indicating the development of anaerobic conditions at tissue level in the stressed crab. Cytochrome C oxidase and Mg2+ ATPase activity levels were also decreased, indicating the impaired energy synthesis and prevalence of energy crisis. These results suggest that fenvalerate has a profound effect on the glucose metabolism of crab.     

Alterations in Carbohydrate Metabolism in Selected Tissues of Crab,Oziotelphusa Senex Senex (Fabricius) Under Fenvalerate-Induced Stress

Changes in carbohydrate metabolism in hepatopancreas and muscle of the crab, Oziotelphusa senex senex exposed to a sublethal concentration (0.2 ppm) of fenvalerate, a pyrethroid insecticide, were studied. the glycogen and total carbohydrate levels decreased significantly in the tissues of crab exposed to fenvalerate. an increase in phosphorylase ‘a’ and decrease in aldolase activity levels suggested increased glycogenolysis, and decreased glycolysis during fenvalerate toxicity. Krebs cycle enzymes such as NAD-isocitrate dehydrogenase, succinate dehydrogenase and malate dehydrogenase were decreased, suggesting reduced mitochondrial oxidative metabolism. Glucose-6-phosphate dehydrogenase activity was increased significantly, indicating enhanced oxidation of glucose through the hexose monophosphate shunt pathway. Lactate dehydrogenase activity was elevated indicating the development of anaerobic conditions at tissue level in the stressed crab. Cytochrome C oxidase and Mg2+ ATPase activity levels were also decreased, indicating the impaired energy synthesis and prevalence of energy crisis. These results suggest that fenvalerate has a profound effect on the glucose metabolism of crab.     

Host glutamine synthetase activities in the giant clam—zooxanthellae symbiosis: effects of clam size,elevated ammonia and continuous darkness

Host tissues and zooxanthellae of the giant clam Tridacna gigas contained glutamine synthetase, with the highest transferase activities present in the gill, followed by the kidney, mantle, zooxanthellae, foot, heart and adductor muscle, in that order. Synthetase activities of glutamine synthetase in host tissues and zooxanthellae were in a similar order, but the differences were not so marked. Host tissues also contained hexokinase, glucose-6-phosphate dehydrogenase and malate dehydrogenase. Highest hexokinase activities were present in the heart, followed, in order, by the gill, mantle, adductor muscle and foot. Highest glucose-6-phosphate dehydrogenase activities were present in the gill, followed by the mantle, heart, adductor muscle and foot. All tissues assayed contained high malate dehydrogenase activities. There was no detectable glutamate dehydrogenase activity. Glutamine synthetase activity in gill and mantle tissue decreased by 1.6% with every 1 cm increase in clam size. Host glutamine synthetase activity decreased by 80% in gill tissue and by 45% in mantle tissue in clams which were maintained for 8 d in continuous darkness. Similar effects were found when clams were kept in light in the presence of elevated ammonia concentrations. It is suggested that both host and symbionts are nitrogen-deficient in small clams and that host glutamine synthetase plays a role in ammonia assimilation by the intact association.     

Anti-implantation and anti-fertility potentials of Anethum graveolens L. extracts in rats

Ovarian hormones affected some enzymes in reproductive tissues. Previous studies revealed Anethum graveolens (dill) seed extract elevated ovarian hormones. In this study, we compared the effects of dill seed and leaf extracts on some enzymes activities and infertility potential. Female Wistar rats were divided into three groups of control, dill seed and dill leaf aqueous extracts treated groups. Experimental groups received 1 mL of 0.5 g kg^?1 of each extract orally for 25 days (five estrous cycles). Estradiol, progesterone, luteinizing hormone, and follicle stimulating hormone concentrations were determined. Uterus and ovaries were removed and their glucose-6-phosphate dehydrogenase, lactate dehydrogenase, and alkaline phosphatase activities were measured. Female rats of three groups were mated with untreated males. Fetuses were extracted in the 20th gestational day and their weights and crown rump lengths were measured. Anti-fertility and anti-implantation activities and fertility indices were calculated. Glucose-6-phosphate activity of dill seed treated group increased 1.6 times in the endometrium and 1.7 times in the myometrium. Progesterone concentration and lactate dehydrogenase activity of serum increased in the dill seed treated group compared to the control and dill leaf treated group. A significant decrease was observed in weights and crown rump lengths of fetuses, weights of placenta, and fertility index of the dill seed treated group compared to the control and dill leaf treated group, but its anti-implantation and anti-fertility indices increased. We suggested that high level of glucose-6-phosphate could entail increased oxidative stress in uterus and ovary. High lactate dehydrogenase activity in serum may affect cell membranes. Higher secretion of progesterone caused hormonal imbalance and produced estrous cycle irregularity. It was concluded that dill seed but not dill leaf extract could induce infertility in an animal model.     

Molecular mechanisms of adaptation to low temperature in marine poikilotherms. Some regulatory properties of dehydrogenases from two arctic species

The properties of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase from gill tissue of the tanner crab Chionocetes bairdi, and lactate dehydrogenase (LDH) and glyceraldehyde dehydrogenase from skeletal muscle of C. bairdi and the yellowfin sole Limanda aspera were examined over the physiological temperature range of the animals. Both animals were obtained in the Bering Sea in winter, and their enzymes appear to be remarkably cold-adapted. Affinity of sole LDH for substrate appears to increase with decreasing temperature, thus keeping reaction rate essentially independent of temperature at physiological concentrations of the substrate. Calculated values of activation energy are low, in keeping with the argument that organisms from cold environments have enzymes with a reduced energy of activation. In addition, Hill plots of the substrate saturation curves for lactate dehydrogenase from muscle of sole indicate that there is a facilitation of allosteric behaviour at low temperatures. Maximum affinity of sole LDH for substrate in the absence of univalent cations occurs at 3°C, while in the presence of 150 mN K⁺, it occurs between 0° to-2°C. The effects of Mg²⁺ on enzyme activity appear to be determined by concentration of substrate and temperature. Thus, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase are stimulated more effectively by Mg²⁺ at low temperature and at low substrate levels whereas, at high concentrations of substrate, they are relatively independent of the bivalent cation. All four dehydrogenases are affected by the univalent cations Na⁺, K⁺ and NH₄ ⁺ in a manner which appears to be determined, in part at least, by concentration of substrate and by temperature. These findings suggest mechanisms for the maintenance and regulation of enzyme activity in poikilothermic tissues at low and changing temperatures.     

Glucose-6-phosphate dehydrogenase and thermal acclimation in the mullet fish

Glucose-6-phosphate dehydrogenase in mullet liver (Mugil cephalus L.) occurs in 2 electrophoretically distinguishable forms, termed I and II. Both are tetramers (at neutral pH) with molecular weights greater than 200,000. At pH 9, each tetramer dissociates into two dimer molecules which retain catalytic activity. At intermediate pH values, an equilibrium tetramer dimer mixture probably occurs. Kinetic studies of Form I indicate that it is strongly inhibited by TPNH, which is competitive with respect to both G6P and TPN. Inhibition is greatly increased at high temperatures while enzyme-substrate and enzymeecoenzyme affinities greatly decrease. These properties strongly favor glucose-6-phosphate dehydrogenase function at low temperature, a situation that is partly compensated for during warm acclimation by an increase in the relative importance of Form II. Although Form II displays catalytic and regulatory properties which are qualitatively similar to those of Form I, it is able to outcompete Form I for limiting substrate at high temperatures.     

Studies on the nutrition of marine flatfish. The effect of dietary protein content on certain cell components and enzymes in the liver of Pleuronectes platessa

In order to examine the effects of artificial diets at the tissue level, plaice (Pleuronectes platessa L.) were fed either high (50%) or low (20%) protein diets for several weeks and the total quantities of deoxyribonucleic acid (DNA), ribonucleic acid (RNA), protein and phospholipid in their livers were measured. Alanine amino-transferase, aspartate aminotransferase, glutamate dehydrogenase and glucose-6-phosphatase activities in the livers were also measured. Similar measurements were made on the livers of wild plaice. The total amount of DNA in the livers of both cultured and wild plaice, of standard weight, did not differ significantly, irrespective of dietary history. In fish of standard weight, total hepatic RNA, protein and phospholipid levels were highest in the cultured fish fed high protein diet and lowest in the wild fish. These differences were related to dietary protein supply and environmental temperature. The total organ levels of the liver enzymes in plaice of equal weight were not significantly different in the cultured fish fed high and low protein diets. Wild-fish livers contained a smaller total amount of alanine aminotransferase, aspartate aminotransferase and glucose-6-phosphatase activity than did those of cultured fish. Total liver glutamate dehydrogenase activity was not significantly different in any of the fish examined. It is suggested that kinetic and allosteric factors may be more important in controlling protein metabolism and amino acid cat abolism in fish than total enzyme level.     

Studies on the biology of the red sea bream Chrysophrys major III. Metabolic response to starvation in different salinities

Red sea breams were kept at 20°C without food at 3 salinities (full sea water, 950 mOsm kg^-1; 2/3 sea water, 640 mOsm kg^-1; 1/3 sea water, 330 mOsm kg^-1). In fish adapted to all 3 salinities, starvation resulted in marked decline of plasma FFA and -hydroxybutyrate and liver glycogen levels but plasma glucose and lactate concentrations were maintained. These findings suggest that with the onset of starvation, enhanced hepatic glycogenolysis and decreased fat utilization occurred. Fish, adapted to full and 2/3 sea water, could not survive for more than 19 d without food. However, fish adapted to 1/3 sea water could tolerate 27 d of starvation. Enhanced survival during starvation in 1/3 sea water was observed to be associated with maintenance of plasma protein and elevation of hepatic glucose-6-phosphate dehydrogenase activity. It is suggested that sea breams be transferred to an iso-osmotic medium whenever the threat of starvation prevails, but this suggestion has yet to be evaluated in economic terms.Please communicate with Dr. Norman Y. S. Woo     

Metabolic enzymes in coelomic cells (eleocytes) of the polychaete Nereis virens: sex specific changes during sexual maturation

The activities of some enzymes of the intermediary metabolism and the content of soluble protein and carbohydrate (glycogen plus free glucose) were measured in one type of coelomic cells (eleocytes) of the polychaete Nereis virens. Specimens used in this study were collected between 1989 and 1991 in Oosterscheldt Bay, The Netherlands, and divided into six different stages of sexual maturation as determined by the mean oocyte volume. In both sexes, the soluble protein content in eleocytes of immature individuals (11 mg ml^–1 cell vol) increased three-fold. In prespawning N. virens the soluble protein content decreased to less than 2 mg protein ml^–1 cell vol in females but not in males. In both sexes, the carbohydrate content decreased continuously from immature [300 mol glucose equivalent (equiv) ml^–1 cell vol] to prespawning individuals (< 40 mol glucose equiv ml^–1 cell vol). During the time course of maturation, the specific activities (expressed as units mg^–1 protein) of pyruvate kinase, phosphoenolpyruvate carboxykinase, malate dehydrogenase, alanine aminotransferase and glutamate dehydrogenase decreased in both sexes. A transient increase in the specific activities was found for glycogen phosphorylase and aspartate aminotransferase. No major changes were found for hexokinase, lactase dehydrogenase, glucose-6-phosphate dehydrogenase and malic enzyme. Sex specific differences were found for the activities of citrate synthase and isocitrate dehydrogenase, which were higher in males. the specific activities of the latter enzyme increased more than ten-fold in males, but only four-fold in female eleocytes during maturation. In eleocytes of prespawning females, the activities of most enzymes showed extremely high variations not found in prespawning males. For two enzymes of fatty acid catabolism, -hydroxyacyl-CoA dehydrogenase and -hydroxybutyrate dehydrogenase, only traces of activities were detected, suggesting the absence of significant fatty acid catabolism in the eleocytes. Compared to the eleocytes, the body wall tissue showed ten-fold higher activities of phosphofructokinase, whereas the eleocytes displayed higher activities of the amino acid interconverting enzymes glutamate dehydrogenase and alanine aminotransferase and the glyconeogenic enzyme phosphoenolpyruvate carboxykinase. Citrate synthase activities were similar for both tissues. In the coelomic fluid of N. virens, glucose (< 0.1 to 3.5 mM) and d-lactate (0.1 to 4 mM) were present and represent exogenous substrates for the eleocyte metabolism.     

Metabolic integration between symbiotic cyanobacteria and sponges: a possible mechanism

Metabolic relationships between symbiotic cyanobacteria and host sponge have been investigated in the marine species Chondrilla nucula and Petrosia ficiformis (collected in the Ligurian Sea in 1992). DNA, RNA, total protein, cytosolic protein, total sugar, cytosolic sugar, total lipid, nonprotein sulfhydryl groups, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase were assayed in cortex-free sponge tissue, where cyanobacteria are all but absent. For both species, biochemical parameters were determined in specimens living in illuminated habitats and in dark caves, where sponges are virtually aposymbiotic for cyanobacteria. As C. nucula is unable to colonize dark sites, specimens of this species were artificially transferred to a cave and maintained in dark conditions for 6 mo. Results showed that in the absence of light (i.e., in the absence of cyanobacteria) C. nucula undergo metabolic collapse and thiol depletion. In contrast, P. ficiformis activates heterotrophic metabolism and mechanisms which balance the loss of cell reducing power. This suggests that cyanobacteria effectively participate in controlling the redox potential of the host cells by the transfer of reducing equivalents. Only P. ficiformis is capable of counteracting, by means of heterotrophic metabolism, the loss of the contribution from symbionts which is caused by dark conditions. This explains the differences in the ecological requirements of the two species. Because cyanobacterial symbionts release fixed carbon in the form of glycerol and other small organic phosphate (Wilkinson 1979), a model based on the glycerol 3-phosphate shuttle (typically occurring in chloroplasts and mitochondria) is suggested. The mechanism proposed appears to be an ancient biochemical adaptation which arose among ancestral symbiotic systems, and further developed in the relationships between endosymbiotic organelles and cytoplasm.     

Nukleinsäure- und substratgehalte in der dorsalen rumpfmuskulatur von teleosteern während eines „biologischen stress”

Two teleosts were subjected to extreme biological stimuli: Idus idus L. (6 to 7 cm) to predators (perches or a catfish, 15 to 22 cm) or to an alarm pheromone (skin extract), and male Betta splendens Regan (6 to 8 cm) to fighting each other. Uniform alterations occurred in nucleic acid contents (I. idus) and substrate levels (both species) of the epaxial muscle. In acute stress situations, the nucleic acid content and lactate: pyruvate (L:P) ratio remained unchanged; lactate, pyruvate and glucose-6-phosphate (G-6-P) levels increased to about 200% of those in controls. After an insignificant reduction (or a few minutes constancy), glucose increased to the same extent. In chronic stress situations, lactate, glucose and G-6-P levels remained elevated, L:P increased to about 200%. The pyruvate level and ribonucleic acid:deoxyribonucleic acid (RNA:DNA) ratio decreased significantly (by a maximum of 20%), DNA per gramme wet weight fell insignificantly by about 6%. Substrate alterations, especially the increase in L:P, were similar to those observed post mortem in fish muscle (I. idus), indicating an insufficient oxygen supply in chronic stress situations. Nucleic acid and substrate alterations, probably induced by an increased discharge of catecholamines and glucocorticoids, are interpreted in terms of stress effects.     

Protein composition of white skeletal muscle from mesopelagic fishes having different water and protein contents

The consequences for white skeletal muscle of the whole body variation in water and protein content were examined in 11 mesopelagic fishes taken off the coast of Oregon, USA, in 1983. For such muscles, water content varied from 71 to 91% of muscle wet weight, and protein content ranged from 56 to 141 mg g^-1 muscle wet weight, depending on the species. Dilution by increased water content did not account for the decrease in protein content. Total muscle protein was partitioned into soluble (myogen or sarcoplasmic) and insoluble (myofibrillar) components. Both the myogen and myofibrillar components are reduced in muscle with decreased protein content. The activities (units g^-1 wet wt) of white muscle L-lactate dehydrogenase and L-malate dehydrogenase are higher in fishes undergoing diel vertical migration to surface waters than in fishes that either do not migrate or do not migrate to surface waters. The differences in enzyme activities are not due to a general dilution of muscle protein. The actin content of white skeletal muscle was maintained at a relatively constant level in all 11 species examined and was similar to actin levels observed previously in the white skeletal muscle of scombrids and demersal fishes. This conservation of actin content requires species with a reduced muscle protein content to maintain a significant fraction of their total protein as actin. The specific activities of the myofibrillar Mg²⁺–Ca²⁺-activated adenosine triphosphatases of the mesopelagic species are similar in all 11 species studied. Thus, the ratios of proteins in the isolated myofibrils are probably similar. These results suggest that, in species with decreased muscle protein, there is an increase in the non-myofibrillar form of actin.     

Blood sugar metabolism during moulting in the isopod crustacean Ligia exotica

Blood sugar metabolism of the isopod Ligia exotica Roux was studied in relation to chitin synthesis during the moult cycle. The blood sugars were found to occur free, as well as bound with blood proteins, during all moult stages, as in Emerita asiatica. The variety of free blood sugars is smaller in L. exotica; it comprises only glucose and glucose-6-phosphate. The protein-bound blood sugars are glucose and glucosamine. The blood-volume values do not differ markedly during the moult cycle. Estimations of blood sugars showed a marked rise of sugar levels in the blood during the premoult phase, and a subsequent fall during the freshmoult phase, when chitin is actively synthesised. The chitin values also showed a definite correlation with the blood-sugar values. The increased resorption of chitin during the premoult stage, and its liberation into the blood stream as glucosamine, is indicative of its reutilisation in chitin synthesis as in E. asiatica and the genus Cecropia. As more immediate precursors of chitin, such as uridine diphosphate and uridine diphophate acetylglucosamine compounds, were absent in the blood, a thorough biochemical study of the epidermis is suggested to locate the intermediate precursors of chitin which are possibly derived from blood sugars.     

Observations on the embryonic development and energy source in the crab Xantho bidentatus

During development of Xantho bidentatus, ten stages of the eggs have been recognised. In this period the colour of the egg changes from black to pale white at the X stage of development. Total carbohydrate, glycogen, soluble protein, insoluble protein, total lipid, ash and water content have been determined in all ten stages of developing eggs. The utilisation of these compounds at various stages of development is discussed. The habitat of the crabs and its significance during development is also discussed. A constant decrease in the organic material as well as the dry weight of the egg was noticed with increased stage of development. Along with this a steady increase in the water and ash content was also observed. Glycogen was reduced during early days of development, whereas lipid was reduced during the latter stages of development. Both soluble and insoluble proteins exhibit conspicuous variations depending upon the stage of development.     

外源和内源呼吸模式下好氧活性污泥的微生物群落演替及生物活性特征

通过模拟好氧活性污泥实验,采用PCR-DGGE技术并监测不同时期的CODCr、脱氢酶和总蛋白质的质量浓度,研究在外源和内源呼吸模式下,微生物群落结构及相关生物活性的变化。结果表明：未添加碳源处理中 CODCr的质量浓度稳定在100 mg·L-1左右;脱氢酶的质量浓度从1μg·mL-1降低到接近0μg·mL-1;总蛋白的质量浓度从0.05 mg·mL-1上升至0.07 mg·mL-1后下降至0.01 mg·mL-1左右;同时,微生物群落结构变化不大。外加葡萄糖处理中CODCr的质量浓度从1000 mg·L-1下降并稳定在100 mg·L-1左右;脱氢酶的质量浓度从2μg·mL-1上升到5μg·mL-1;总蛋白的质量浓度均从0.05 mg·mL-1上升至0.07 mg·mL-1后下降至0.005 mg·mL-1左右;同时,微生物群落多样性呈现收敛趋势。内源和外源呼吸模式下的活性污泥中,变形菌门（ Proteobacteria ）都是绝对优势种群,其次是拟杆菌门（ Bacteroidetes ）。内源呼吸末期δ-变形菌门（Deltaproteobacteria）消失,外源呼吸末期硝化螺菌门（Nitrospirae）消失。     

Sub-lethal toxic effects of deltamethrin on blood biochemical parameters of Japanese quail,Coturnix japonica

Feeding deltamethrin-contaminated grains to domestic poultry, such as quails may result in toxic effects in these birds. This study was done to investigate the effects of recommended doses of deltamethrin, sometimes used in grain storage silos, on Japanese quail (Coturnix japonica). Quails were fed grains contaminated with 0.25 and 0.50 mg deltamethrin per kg diet for 21 days and the effects on survival and blood biochemical parameters were studied. Plasma uric acid, creatinine levels, and creatinine phosphokinase activity in the blood were increased. Aspartate aminotransferase and lactate dehydrogenase activities and glucose levels significantly increased in birds treated with the high dose of deltamethrin. Alanine aminotransferase activity and albumin or cholesterol levels were not changed, and acetylcholinesterase and alkaline phosphatase activities, total protein and globulin in plasma were decreased. Administration of 0.25 mg/kg deltamethrin caused increased blood triglyceride levels, 0.50 mg/kg deltamethrin decreased triglyceride levels.     

Overlapping defense responses to water limitation and pathogen attack and their consequences for resistance to powdery mildew disease in garlic mustard, Alliaria petiolata

Plant responses to abiotic stress can alter their response to biotic stress. We examined changes in the activity of several defense proteins in response to powdery mildew infection of garlic mustard (Alliaria petiolata) in the greenhouse and in the field. Second, we examined the effects of water limitation on the same defense protein responses, as well as on total soluble protein and glucose concentration, plant growth, and powdery mildew disease development. Similar increases in the activity of peroxidase, chitinase, and β-1-3-glucanase were observed in leaves of plants with substantial powdery mildew disease in both greenhouse- and field-grown plants. In the greenhouse, activities of chitinase and peroxidase as well as total soluble protein and glucose concentrations generally increased with the degree of water limitation. In turn, leaf growth and powdery mildew symptom development decreased as the degree of water limitation increased. This study revealed that plant chemical responses to water limitation and powdery mildew disease can overlap to a large extent, which, in addition to changing microenvironmental conditions and other indicators of plant quality, may underlie the ability of water limitation to inhibit powdery mildew disease symptom development in this wild plant pathosystem.     

Are there two species of the polychaete genus Marenzelleria in Europe?

North Sea and Baltic Sea populations of the introduced polychaete Marenzelleria viridis (Verrill, 1873) reproduce at different times (spring and autumn, respectively). Enzyme separation by starch gel electrophoresis revealed major differences between specimens from the Baltic Sea and those from the North Sea (collected in 1992 and 1993) but a high degree of homogeneity among populations from the same sea. Three enzyme loci, glucose-6-phosphate isomerase (GPI-A, GPI-B) and malate dehydrogenase (MDH), were fixed to 100% by different alleles in the North and Baltic Sea populations, respectively. Different alleles are dominant for mitochondrial aspartate aminotransferase (mAAT) with allele frequencies of ca. 0.97 in all sampled populations from the North Sea and Baltic Sea, respectively, but heterozygotes were found in all populations. These genetic differences could be due to environmentally induced selection or genetically different origins of the populations, suggesting that populations of the genus Marenzelleria in the North and Baltic Seas may be two different species.     

Effects of carbaryl on the aminotransferases in the mid gut of blister beetle,Mylabris pustulata (Thunb)

The activity levels of aminotransferases such as alanine aminotransferases (AlAT), aspartate aminotransferases (AAT), isoleucine aminotranferases (IlAT), leucine aminotransferases (LAT), valine aminotrasferases (VAT) were measured in the mid gut of the blister beetle; Mylabris pustulata (Thunb) exposed to sublethal doses of carbaryl. The insecticide markedly inhibited the activity levels of all aminotransferases exposed for either short or prolonged treatments. The beetles regained normal enzymic activity after withdrawal from the treatment. It is possible that chronic exposures of beetles to carbaryl may induce impairment in protein synthesis in the mid gut of the beetle.     

Nickel induced changes on some aspects of protein metabolism in the tissues of Pila globosa

Some aspects of protein metabolism were studied in foot, hepatopancreas and mantle tissues of snail, Pila globosa on exposure to lethal concentration for 2 days (336.7 mg/L) and sublethal concentration (67.34 mg/L) of nickel for 1, 5 and 10 days. Total, structural and soluble proteins decreased significantly and to continence, this the levels of amino acids and protease activity increased in all the tissues of snail at all time points examined. Activities of AAT (Aspartate aminotransferase) and AlAT (Alanine aminotransferase) showed contrasting trends of inhibition and elevation during lethal and sublethal concentrations of nickel treatment. GDH (Glutamate dehydrogenase) activity was increased in all the tissues with increase in exposure time. Level of ammonia decreased in snails at sublethal concentration, but increment was observed in lethal concentration along with increased urea content. Under lethal and sublethal exposures, the changes in all the parameters were more pronounced in hepatopancreas followed by foot and mantle. At most instances, snails in the lethal medium were affected more compared to sublethal concentration.