End Of Starvation Research Articles

Changes in the midgut cells in the European cave spider, Meta menardi, during starvation in spring and autumn.

During the growth period, in surface habitats, spiders catch enough prey to feed normally. In contrast, in the cave entrance zone, prey may be relatively scarce. Meta menardi inhabits this cave section, resulting in temporary starvation. We studied structural changes in the midgut epithelial cells of M. menardi during a short-term and a medium-term controlled starvation to mimic the occasional starvation in caves, during spring and autumn. Digestive cells, secretory cells and adipocytes were examined before the experimental starvation, in the middle and at the end of starvation. We used light microscopy, transmission electron microscopy and specific histochemical methods for the detection of lipids, polysaccharides and proteins. Detection of lysosomes, autolysosomes and apoptosis was also carried out. The general structures of the cells did not change during the experimental starvation in either season, while some specific differences in the ultrastructure were observed. In both sexes, in both seasons, the amounts of lipids, glycogen and proteins decreased during starvation. Larger amounts of lipids were found in autumn, while there were no significant differences in the amounts of glycogen and proteins. In both sexes, in both seasons, autophagy and apoptosis intensified with starvation in progress, but more intensively in females. Thus, autumn individuals, in contrast to spring ones, compile energy-supplying stores to confront the subsequent winter deficiency of prey in caves, while the cellular ultrastructures undergo the same starvation-dependant changes at any time during the growth period.

Effects of short-term starvation and re-feeding on antioxidant defense status in Mesopotamichthys sharpeyi (Günther, 1874) fingerlings

The objective of this study was to evaluate the impact of short-term starvation and re-feeding on oxidative stress in Mesopotamichthys sharpeyi (Gunther, 1874). After two weeks adaptation to new conditions, a total number of 270 fingerlings were distributed into nine 300-L fiberglass tanks, equipped with aeration system in three treatments including 4, 8 and 16 days starvation (each in 3 replicates). After starvation, all groups were fed for 32 days. At the beginning of trial and at the end of starvation and re-feeding periods, blood samples were collected, plasma was separated and activity of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPX) and malondialdehyde (MDA) content were assayed. Based on the results, no significant difference was observed in SOD activity at the end of starvation and also after re-feeding between the different treatments. At the end of starvation the activity of the CAT and GPX increased significantly in 8 and 16 days of starvation groups compared to the base. Moreover, a significant increase in MDA levels of plasma was found during food deprivation. These findings showed that short-time starvation increased antioxidant enzymes activity in plasma of M. sharpeyi but short-term food deprivation and re-feeding periods in this species does not cause disturbances in the antioxidant defense status.

Effects of starvation on growth, survival, and body biochemical composition among different sizes of Manila clam Ruditapes philippinarum

A study was conducted to investigate the impact of starvation on different sizes of Manila clam Ruditapes philippinarum (0.66 ± 0.11, 2.12 ± 0.38, and 11.65 ± 0.84 mm in shell length, respectively) in the summer of 2008. Different size clams were starved for 7, 15, 30, 45, and 60 d, respectively, and followed by refeeding for 30 d. During the study, the water temperature ranged 26.2–28.4 °C, salinity 22–24‰, and pH 7.80–8.12. Compensatory growth occurred in the smallest size-group after 7 and 15 d of starvation, respectively. The point-of-no-return (PNR 50) was determined to be 18.7 d. However, no compensatory growth was noted in the medium size-group, and the PNR 50 for this group was 25.2 d. The complete compensatory growth was observed for the largest size-group following food depravation for 7 and 30 d, respectively. In the same group, over-compensatory growth occurred 15 d post-starvation. The PNR 50 for the largest size-group was 46.3 d. The survival rate of different groups decreased as the starvation time prolonged. To discuss the change in body biochemical composition of individuals in the process of starvation and refeeding, the biochemical composition of the largest group individuals at different stages was determined. There were no significant differences in moisture and ash concentrations of the largest size-group during starvation and refeeding ( P > 0.05). The relative body protein content increased as the starvation period prolonged and the level returned to normal after refeeding. The lipid content of the clam at the end of starvation was significantly lower than the initial level ( P < 0.05), and remained below the initial level at end of the refeeding period.

Weak compensatory growth makes short-term starvation an unsuitable technique to mitigate body deformities of Tinca tinca juveniles in intensive culture

Juvenile tench, Tinca tinca (L.) (initial mean weight 0.67 g) were continuously fed at high (5.0% of fish biomass) or low (2.5% of fish biomass) daily doses of a commercial formulated diet, or starved for 6 days, then fed these doses. The experiment lasted 40 days. Visible skeletal deformities occurred in fish fed the high doses, and the 6-day food deprivation mitigated the percentage of deformed fish from 37.3 to 12.1%. Deformities were associated with higher condition coefficient value. Faster growing individuals were more susceptible to body malformations within the feeding groups. No compensatory growth in body weight was observed in juveniles fed high or low doses. Lack of compensation was supported by lower carbon/nitrogen ratio in starved-re-alimented fish. Morphometric indices (condition coefficient and height/length ratio) suggested only partial compensation observed mostly during the first few days after the end of starvation. The possible mechanisms underlying this weak compensatory response in T. tinca juveniles may be associated with their slow growth rate and low oxygen consumption. Short starvation mitigates body deformities in intensively fed tench juveniles, however, this technique is not recommended in aquaculture due to their weak compensatory growth response.

Effect of long term anaerobic and intermittent anaerobic/aerobic starvation on aerobic granules

The effect of long term anaerobic and intermittent anaerobic/aerobic starvation on the structure and activity of aerobic granules was studied. Aerobic granular sludge treating abattoir wastewater and achieving high levels of nutrient removal was subjected to 4–5 week starvation under anaerobic and intermittent anaerobic/aerobic conditions. Microscopic pictures of granules at the beginning of the starvation period presented a round and compact surface morphology with a much defined external perimeter. Under both starvation conditions, the morphology changed at the end of starvation with the external border of the granules surrounded by floppy materials. The loss of granular compactness was faster and more pronounced under anaerobic/aerobic starvation conditions. The release of Ca 2+ at the onset of anaerobic/aerobic starvation suggests a degradation of extracellular polymeric substances. The activity of ammonia oxidizing bacteria was reduced by 20 and 36% during anaerobic and intermittent anaerobic/aerobic starvation, respectively. When fresh wastewater was reintroduced, the granules recovered their initial morphology within 1 week of normal operation and the nutrient removal activity recovered fully in 3 weeks. The results show that both anaerobic and intermittent anaerobic/aerobic conditions are suitable for maintaining granule structure and activity during starvation.

Influence of nutritional stress on digestive enzyme activities in juveniles of two marine clam species, Ruditapes decussatus and Venerupis pullastra

The potential use of digestive activities as indicators of the nutritional status in bivalves is discussed in relation to the results obtained in two clam species exposed to starvation and refeeding. Activities of some digestive enzymes (amylase, laminarinase, cellulase, and protease) were measured in juveniles of two commercially interesting species of clams, Ruditapes decussatus and Venerupis pullastra. The specimens were fed normally, being after subjected to a 15-days starvation and a further refeeding period. Samples were obtained at different moments of such feeding schedule to evaluate enzymes as well as weight (live, dry and organic) and length, in order to calculate growth rates and feeding efficiencies. Starvation led to a major decrease in clam growth as measured by dry weight and a negative growth as measured by organic weight, this coinciding with a certain degree of growth of the shell and a consumption of soft tissue. This response occurred more rapidly in R. decussatus but was of a lower magnitude than in V. pullastra. Activity of carbohydrases decreased rapidly in both species with starvation, although protease activity was maintained in R. decussatus. Recovery after the end of starvation was not similar in both species; while R. decussatus attained similar growth rates and enzyme activities to those measured prior to nutritional stress, V. pullastra only recovered 50% of its initial values. For both species of bivalves it can be concluded that digestive enzymes, and more specifically amylase, could be used as indicative of their nutritional condition.

Oral Carbohydrate Solution Ameliorates Endotoxemia-Induced Splanchnic Ischemia

The purpose of this study was to investigate the effect of oral administration of a simple carbohydrate solution on splanchnic circulation and bacterial translocation in endotoxemia. Group 1 was sham control; group 2 was starved for 24 hours; in group 3, endotoxin was administrated at the end of starvation; in group 4, carbohydrate solution was administrated via orogastric route for 24 hours; and in group 5, carbohydrate solution was given and endotoxin was administrated at the end of 24 hours. Splanchnic blood flows were recorded and tissue samples were collected for microbiological analyses. There was a significant increase (P<.05) in the incidence of bacterial translocation in starvation. Endotoxemia decreased distal (P=.021) and midmesenteric (P=.046) flow in starved animals. Oral carbohydrate significantly increased ileal blood flow in starvation (P=.036) and endotoxemia (P=.008). In conclusion, oral carbohydrate solution prevents bacterial translocation during starvation and endotoxemia. The possible mechanism is the improvement in the mesenteric blood flow.

Exceptional long-term starvation ability and sites of lipid storage of the Arctic pteropod Clione limacina

The Arctic pteropod Clione limacina was collected in Kongsfjorden, Svalbard, in mid June 2004, to study the lipid metabolism within the sites of lipid storage structures during long-term starvation. Animals survived in an aquarium without any food for nearly 1 year (356 days). Size, number of lipid droplets, dry and lipid mass, lipid class and fatty acid compositions of C. limacina were determined and separately analysed for the digestive gland and the remaining integument. During the starvation period, animals shrunk from 22.4 to 12 mm in length on average, and the number of lipid droplets decreased from 1,600 to 1,000 per animal. Dry mass (DM) and total lipid mass both dropped by about 80% from day 200 to the end. The lipid content as percentage DM of the total organism did not decrease significantly ranging from 43.8 to 32.3%DM. The lipid content of the trunk was moderate with about 20%DM. The digestive gland was very rich in lipids with more than 70%DM throughout the experiment and is the major site of lipid metabolism and storage. Triacylglycerols (TAG) decreased, in the total organism, from high initial levels of 62.6 to 43% of total lipid at the end. In contrast, the proportions of 1-O-alkyldiacylglycerols [diacylglycerol ethers (DAGE)] remained almost constant, varying between 20.4 and 28.4%. In the digestive gland, TAG ranged from 60.3 to 64.8% and DAGE from 23.6 to 32.2% from day 200 to the end of the experiment. TAG and DAGE of the trunk were most likely located in the lipid droplets and were almost depleted at the end of starvation. Besides their function as lipid deposit DAGE may also act as protecting substance against bacterial and fungal infections. During the first 200 days of starvation, the fatty acid compositions showed only small variations. Thereafter, fatty acids typical for storage lipids decreased in all body compartments. In adaptation to long periods of food scarcity, C. limacina has evolved various strategies as body shrinkage, utilisation of body constituents not essential for survival, a very low metabolism and slow lipid consumption.

The role of juvenile hormone in the control of reproductive function in Drosophila virilis under nutritional stress

To investigate the role of juvenile hormone (JH) in the control of Drosophila reproduction under stress, JH degradation and reproduction were studied under nutritional stress and JH treatment in Drosophila virilis females of wild type ( wt) and a heat stress ( hs) mutant: this mutant does not respond to heat stress by alterations in JH metabolism and has decreased JH level and fertility under normal conditions. One day of starvation results in a decrease of JH degradation, a delay in oocyte maturation, degradation of early vitellogenic egg chambers, accumulation of mature oocytes and a 24 h oviposition arrest in both wt and hs females. A fertility decrease was observed in both wt and hs females 24 h following the end of starvation. JH treatment leads to a decrease of JH degradation and an arrest of oviposition for 24 h in fed females. JH treatment prior to starvation seems to protect some oocytes from resorption: in JH-treated wt females, fertility increases rapidly following the end of starvation. The dynamics of JH degradation and fertility are similar following starvation and JH treatment. The role of JH in the accumulation of mature oocytes and the delay of oviposition under stress are discussed.

Differential neuropeptide responses to starvation with ageing.

During starvation, counterregulatory responses to loss of food (i.e. responses that lead to an increase in appetite) occur in the central nervous system (CNS). This study was designed to examine whether middle-aged rats show greater or smaller behavioural, peripheral and central hormonal responses during starvation compared to young rats. In experiment 1, refeeding following 4 days of starvation was measured in both middle-aged (72-week-old) and young (9-week-old) rats. The level of refeeding was similar to each prestarved level until 3 days after the end of starvation in both groups. From the 4th day, the level of refeeding in young rats increased and reached beyond the prestarved level, whereas refeeding in middle-aged rats remained similar to the prestarved level. Thus, overall refeeding throughout 7 days was greater in young rats than in middle-aged rats. In experiment 2, middle-aged and young rats were starved for 4 days and were killed in the morning. Middle-aged rats showed a smaller plasma corticosterone response than that of young rats. The magnitude of decreases in plasma glucose, insulin and leptin was similar in both groups. In the arcuate nucleus, the starvation-induced increase in neuropeptide Y (NPY) mRNA and the decrease in proopiomelanocortin (POMC) mRNA were smaller in middle-aged rats than in young rats. In contrast, the starvation-induced decrease in corticotrophin-releasing hormone (CRH) mRNA in the hypothalamic paraventricular nucleus was greater in middle-aged rats than young rats. The magnitude of decrease in type-2 CRH receptor mRNA in the ventromedial hypothalamus was similar in both groups. The results indicate that (a) ageing impaired refeeding response (b), middle-aged rats showed the same directional neuropeptide mRNA responses as seen in young rats during starvation and (c) the magnitude of these counterregulatory responses in the CNS in middle-aged versus young rats was not uniform, but rather was site-specific or neuropeptide-specific. This study suggests the importance of NPY and POMC responsiveness in the arcuate nucleus in the age-related differences resulting from starvation-induced refeeding.

Protein utilization during starvation in fat and lean Svalbard ptarmigan (Lagopus mutus hyperboreus)

Body protein sparing during starvation has been examined in fat and lean Svalbard ptarmigan. Protein utilization was determined from daily N excretion and from the rate of decrease in body mass. Changes in plasma concentrations of β-hydroxybutyrate, free fatty acids, glucose, and uric acid were also recorded. When fat birds were starved for 15 days protein catabolism initially fell (phase I) and was thereafter kept low (phase II). This was evident from the temporal pattern in both N excretion and body mass loss. In two birds, N excretion eventually increased, revealing enhanced protein catabolism and thus a third phase of starvation. Changes in protein utilization were paralleled by changes in plasma uric acid. Approximately 9% of the energy demand was covered by breakdown of body protein during phase II. The importance of fat catabolism in providing energy was indicated by markedly elevated plasma levels of β-hydroxybutyrate and free fatty acids. When lean birds were starved for 5 days there appeared to be no phase II. The temporal pattern of body mass loss indicated phase I and III but that of N excretion only phase III. The relative contribution of body protein to energy demand increased from 22% at day 2 to 41% at the end of starvation and was paralleled by increased plasma uric acid. When data from lean and fat birds were pooled, the changes in uric acid and N excretion were highly correlated (r=0.92, P<0.001), indicating that plasma uric acid is a reliable index of protein breakdown in starving Svalbard ptarmigan. In conclusion, starving fat Svalbard ptarmigan have a much greater capacity to spare body protein than lean birds. Fat birds effectively reduce protein catabolism and maintain this at a low level whereas starving lean birds increase protein catabolism.

The nutritional regulation of circulating placental lactogen in fetal sheep.

Maternal and fetal plasma ovine placental lactogen (oPL), insulin, and IGF-I levels were measured in response to the starvation and refeeding of pregnant sheep on two defined planes of nutrition. Chronically catheterized pregnant ewes were placed on either a high plane (n = 5) or low plane (n = 5) of nutrition at least 1 wk before the experiment. At 125 to 135 d gestation, the ewes were starved for 72 h and then an i.v. infusion of 10% glucose was administered over 4 h, followed by refeeding at the designated nutritional plane. Plasma oPL levels of fetuses whose mothers had been on a high plane of nutrition were significantly higher during starvation (p less than 0.05) than those of fetuses whose mothers had been on a low plane (high + 0.54 +/- 0.17 and low -0.02 +/- 0.17 nmol/L from mean control levels). Intravenous glucose infusion to the ewes at the end of starvation caused a marked rise in fetal plasma oPL levels in both groups (increments of 2.61 +/- 1.4 nmol/L in the high group and 2.81 +/- 1.16 nmol/L in the low group). Maternal oPL levels did not differ significantly between the two nutritional groups during starvation and did not change during glucose infusion. Fetal and maternal plasma IGF-I levels both fell during starvation. Maternal IGF-I levels fell faster in the high group (-17.9 +/- 4.5 at 24 h versus -4.7 +/- 7.2 nmol/L in the low group), but the groups were not different at the end of starvation.(ABSTRACT TRUNCATED AT 250 WORDS)

Metabolic depression and heat balance in starving Wistar rats

1. 1. Resting metabolic rate and heat balance was studied in rats starved for 8 days at ambient temperature 22°C and 30°C. 2. 2. A depression of the resting metabolic rate was observed, at both temperatures. Metabolic rate depression, expressed as a function of the ratio between the real body wt and the normal body wt, was less at 22°C than at 30°C. 3. 3. Deep body temperature decrements of 2°C and 0.6°C by the end of starvation indicated that central temperature controlling mechanisms were affected. 4. 4. Concurrent decrements of evaporative heat loss did not account for the changes in heat conductance, thus indicating that a reduction of peripheral blood circulation also took part.

Perinatal age determines the severity of retarded lung development induced by starvation.

Susceptibility of the lung to caloric restriction is age-dependent, with more permanent damage occurring during the phases of growth and differentiation. Because the guinea pig is born with more well-developed alveoli than are other rodents, the postnatal lung of this species may better resist alveolar hypoplasia than the prenatal lung. Control animals were raised from sows provided food ad libitum during and after normal gestations (66 to 68 days). Starvation groups received 50% rations of control food intakes during 1 of three 21-day periods: prenatal starvation, with sows rationed during their last trimester (Day 45 to term); neonatal starvation, with nursing sows rationed during the 21 days postpartum before weaning; weanling starvation, with animals starved from 21 to 42 days postpartum. Lungs were fixed in situ with glutaraldehyde and analyzed for pulmonary morphometrics. At the end of starvation and before refeeding, lungs of prenatal and weanling starvation groups were significantly reduced for tissue volumes, alveolar and capillary surface areas, and pulmonary diffusing capacity. Recovery with feeding was complete for most parameters in the starved weanlings by maturity, but animals starved prenatally showed residual starvation effects as adults. The neonatally starved animals showed minimal effects of starvation on lung dimensions, both acutely and as adults. Morphologically, the lungs of some prenatally starved neonates were apparently retarded, at least to the saccular phase, and correlated with significant increases in the number of stillborn litters and in neonatal mortality within hours of parturition.

Sizes of G1 and G2 populations in starved Tetrahymena

Feulgen cytophotometry and autoradiography were used to study DNA content and DNA synthesis in starved and starved-refed Tetrahymena pyriformis GL-C. It was found that (1) the cell population shows a limited increase in cell number during starvation and this increase is restricted to the first 7 h of starvation; (2) at the end of starvation, there is a portion of the cell population whose DNA content is similar to that for standard G2 cells; (3) a significant portion of the dividing cells at the first division following refeeding in the presence of [ 3H]TdR are unlabeled; (4) these unlabeled cells are among the first to divide and, upon division, generally enter into a cell cycle either lacking a G1 phase or with a shortened G1 phase.

Metabolic studies in starvation.

SummaryThree obese females were studied during starvation (0 to 500 Calories per day) and light activity for 18, 28 and 34 days, during which they were given vitamins and liberal amounts of water, and two of them were given electrolytes. Studies were then continued on two subjects given 500 Calorie diets with contained protein.They experienced little or no hunger, and no untoward effects except halitosis, slight ketonuria and sensitivity to cold. Weight loss amounted to 9.3, 14.1 and 9.5 kg., averaging 810, 330, 250 and 250 grammes per day in successive weeks. This was analysed in terms of its components by the methods usually used in metabolic studies and indirect calorimetry.Protein catabolism declined as starvation proceeded to a minimum level of 12 to 25 grammes per day. It was decreased by norethandrolone and by carbohydrate feeding. The average daily losses of protein during succeeding weeks were 55, 36, 28 and 18 grammes. Overall, protein accounted for 7.6% to 9.1% of the weight loss and provided 5.0% to 6.9% of the caloric expenditure. Protein lost during starvation ranged from 704 to 1156 grammes, which represent 2.8 to 4.6 kg. of muscle and other cellular tissues. Creatinine excretion gradually fell; it accounted for about 5% of the nitrogen loss initially and 15% in the later stages.Carbohydrate losses were estimated at 495 to 1050 grammes, accounting for 3.5% to 11.0% of the weight loss and for 3.0% to 6.4% of the Calories. Fat losses amounted to 4.1 to 6.5 kg., being 44% to 68% of the weight loss and providing 87% to 90% of Calories. The average daily loss of fat was 215 grammes. The gaseous exchanges and respiratory quotient fell, and the basal metabolic rate fell more steeply than the body weight or surface area.Water balance was estimated from measurements and calculations made in two slightly different ways, and the total body water was measured in one subject. All items of losses and gains were determined daily, including metabolic water and evaporation. The cumulative net losses of water reached a peak of 6.2 litres in one subject and were 3.8, 6.0 and 1.2 litres at the end of starvation in the three subjects. The final “corrected” water balances, when allowance was made for the discharge of cell water associated with protein catabolism and for possible initial imbalances, were —1.6, —1.1 and +0.5 litres.Serum electrolyte levels showed only minor changes. Potassium, sodium and chloride were apparently retained in store in the two subjects who were given these electrolytes. There was a net loss of potassium in all subjects, but in two the potassium balance was normal when account was taken of electrolytes released from cellular breakdown.Observations from this study and from the literature have been interpreted as emphasizing the idea that (a) negative nitrogen balance means the amputation of cells so that cellular water and electrolytes are released in proportion to the protein catabolized, and (b) the “desirable” or normal water balance recognizes a constant volume of extracellular fluid plus an intracellular volume which is proportionate to the cellular protein mass. This concept, the nature of obesity tissue, nitrogen metabolism and the possible importance of essential amino acids and of creatinine metabolism are discussed.