Photorespiration: metabolic pathways and their role in stress protection

Photorespiration results from the oxygenase reaction catalysed by ribulose-1,5-bisphosphate carboxylase/ oxygenase. In this reaction glycollate-2-phosphate is produced and subsequently metabolized in the photorespiratory pathway to form the Calvin cycle intermediate glycerate-3-phosphate. During this metabolic process, CO2 and NH3 are produced and ATP and reducing equivalents are consumed, thus making photorespiration a wasteful process. However, precisely because of this ine¤ciency, photorespiration could serve as an energy sink preventing the overreduction of the photosynthetic electron transport chain and photoinhibition, especially under stress conditions that lead to reduced rates of photosynthetic CO2 assimilation. Furthermore, photorespiration provides metabolites for other metabolic processes, e.g. glycine for the synthesis of glutathione, which is also involved in stress protection. In this review, we describe the use of photorespiratory mutants to study the control and regulation of photorespiratory pathways. In addition, we discuss the possible role of photorespiration under stress conditions, such as drought, high salt concentrations and high light intensities encountered by alpine plants

Local variation in endoparasite intensities of bank voles (Clethrionomys glareolus )from ecologically similar sites: morphometric and endocrine correlates

Much interest has centred recently on the role of adaptive trade-offs between the immune system and other components of life history in determining resistance and parasite intensities among hosts. Steroid hormones, particularly glucocorticoids and sex steroids, provide a plausible mechanism for mediating such trade-offs. A basic assumption behind the hypothesis, however, is that steroid activity will generally correlate with reduced resistance and thus greater parasite intensities. Here, we present some findings from a field study of bank voles (Clethrionomys glareolus ) in which we have looked at associations between parasite intensities, anatomical and morphometric measures relating to endocrine function and life history variation in three local populations inhabiting similar but mutually isolated woodland habitats. In general, sites with greater parasite intensities were those in which male C. glareolus had significantly larger adrenal glands, testes and seminal vesicles for their age and body size. Females also showed a site difference in adrenal gland weight. Some aspects of site-related parasite intensity were associated with asymmetry in adrenal gland weight and hind foot length, which may have reflected developmental effects on glucocorticoid activity

Variation in the helminth community structure in bank voles (Clethrionomys glareolus) from three comparable localities in the Mazury Lake District region of Poland

We tested the null hypothesis that populations of hosts trapped in isolated neighbouring locations showing comparable habitat quality, should support similar helminth parasite communities. The study was undertaken in a 2-week period in late summer in NE Poland in a single year, thereby eliminating seasonal and between-year variation in parasite burdens. A total of 139 Clethrionomys glareolus (bank vole) were sampled from 3 forest sites of similar habitat quality. Total species richness was 11 (6 nematodes and 5 cestodes) with 85±6% of the voles carrying at least 1 species and an overall mean species richness of 1±4. At the component community level, the fewest species of helminths were recorded from site 2 (n=6, compared with 9 at each of the other sites), but site 3 had the lowest Berger-Parker Dominance Index and the highest Simpson's Index of Diversity. At the infracommunity level, site 3 had the highest mean no. of helminthspecies}vole, the highest mean Brillouin's Index of Diversity but the lowest mean no. of helminths/vole. Voles from sites 1 and 3 differed in the nematodes that were most common (site 1, Heligmosomum mixtum ± 95%; site 3, Heligmosomoides glareoli ± 79±3%). At site 2 no species exceeded 50% but prevalence of Syphacia petrusewiczi was higher than at the other sites. The prevalence of cestodes was too low to test reliably (12±9%), but the highest prevalence of adult cestodes was recorded at site 1 (22±5%compared with 4±9 and 1±7%for sites 2 and 3 respectively). Host sex did not ifluence infection, but mean species richness increased with age. The different sites were responsible for most of the variation in our data, and the intrinsic factors (sex and age) were less important in shaping the component community structure of helminths. We conclude that even locations in relative close proximity to one another (13±25 km), selected on the basis of similar habitat quality, have rodent populations that differ in their helminth parasite communities, although for reasons other than the factors quantified in the present study

Behaviour of uranium along Jucar River (Eastern Spain) Determination of 234U/238U and 235U/238U ratios

The uranium concentration and the U-234/U-238, U-235/U-238 activity ratios were studied in water samples from Jucar River, using low-level alpha-spectrometry. The effects of pH, temperature and salinity were considered and more detailed sampling was done in the neighbourhood of Cofrentes Nuclear plant (Valencia, Spain). Changes were observed in the uranium concentration with the salinity and the U-234/U-238 activity ratio was found to vary with pH. Leaching and dilution, which depend on pH and salinity, are the probable mechanisms for these changes in the concentration of uranium and the activity ratios.Rodríguez Álvarez, MJ.; Sanchez, F. (1995). Behaviour of uranium along Jucar River (Eastern Spain) Determination of 234U/238U and 235U/238U ratios. Journal of Radioanalytical and Nuclear Chemistry. 190(1):113-120. doi:10.1007/BF02035642S1131201901M. J. RORDÍGUEZ-AALVAREZ, F. SÁNCHEZ, E. NAVARRO, Proc. 3nd Intern. Summer School, Huelva Spain, M. GARCÍA-LEÓN, G. MADURGA (Eds), World Scientific, Singapore, 1994.M. IVANOVICH, R. S. HARMON (Eds), Uranium Disequilibrium Series: Applications to Environmental Problems, Clarendon Press, Oxford, 1982.K. OSMOND, J. B. COWART, At. Energy Rev., 14 (1976) 621.B. L. DICKSON, R. L. MEAKINS, Nucl. Instrum. Methods Phys. Res., 223 (1983) 593.J. L. GASCÓN, MURILLO, PhD Thesis, University of Zaragoza, Spain, 1990.M. C. MORÓN, A. MARTINEZ-AGUIRRE, M. GARCÍA-LEÓN, Intern. Conf. on Environmental Radioactivity in the Mediterranean Area, Barcelona 10–13 May 1988, SNE-ENS, Barcelona, 1988, p. 111.R. BOJANOWSKI, R. FUKAI, S. BALLESTRA, H. ASARI, Determination of natural radioactive elements in marine environmental materials by ion-exchange and α-spectrometry. Proc. 4th Symp. on the Determination of Radionuclides in Environmental and Biological Materials, April 1983, London, Ed-Rd Press.R. GARCÍA-TENORIO, M. GARCÍA-LEÓN, G. PIAZZA, Anal. Física B, 82 (1986) 238.L. HALLSTADIUS, Nucl. Instrum. Methods Phys. Res., 223 (1984) 266.F. VERA, A. MARTIN, Nucl. Instrum. Methods Phys. Res., A276 (1989) 289.A. MARTINEZ-AGUIRRE, M. GARCÍA-LEÓN, J. Radioanal. Nucl. Chem., 155 (1991) 97.J. R. DOOLEY, H. C. ROSHOLT, Econ. Geol., 61 (1996) 326.A. MARTINEZ-AGUIRRE, M. GARCÍA-LEÓN, Radiat. Prot. Dosim., 45 (1992) 249.J. TOOLE, M. S. BAXTER, J. THOMSON, Estuarine, Coastal and Shelf Sci., 25 (1987) 283.S. G. BHAT, S. KRISHANASWAMI, Proc. Indian Acad. Sci., A LXX, (1969).K. K. TUREKIAN, J. K. COCHRAN, in: Chemical Oceanography, Vol. 7, J. P. RILEY and R. CHESTER (Eds), 2nd ed., Academic Press, New York, 1978.D. LANGMUIR, Geochim. Cosmochim. Acta, 42 (1978) 547.J. M. MARTIN, M. MEYBECK, Mar. Chem., 7 (1979) 173.Radionuclide Transformations, Annals of the ICRP, ICRP Publication 38, Vol. 11–13, Pergamon Press, 1983.A. MANGINI, G. SONNTAG, G. BERTSCH, E. MÜLLER, Nature, 278 (1979) 337.M. R. SCOTT, in: M. IVANOVICH, R. S. HARMON (Eds), Uranium Disequilibrium Series: Applications to Environmental Problems, Clarendon Press, Oxford, 1982.J. K. OSMOND, J. B. COWART, in: M. IVANOVICH, R. S. HARMON (Eds), Uranium Disequilibrium Series: Applications to Environmental Problems, Clarendon Press, Oxford, 1982.R. BOWEN (Eds), Isotopes in the Earth Sciences, Elsevier Applied Science, 1988.F. VERA, PhD Thesis, University Extremadura, Spain, 1988.F. VERA, A. MARTIN, J. Radioanal. Nucl. Chem., 134 (1988) 73

Synchronous Evolution of Galaxies in Groups: NGC 524 Group

By means of panoramic spectroscopy at the SAO RAS BTA telescope, we investigated the properties of stellar populations in the central regions of five early-type galaxies -- the NGC 524 group members. The evolution of the central regions of galaxies looks synchronized: the average age of stars in the bulges of all the five galaxies lies in the range of 3--6 Gyr. Four of the five galaxies revealed synchronized bursts of star formation in the nuclei 1--2 Gyr ago. The only galaxy, in which the ages of stellar population in the nucleus and in the bulge coincide (i.e. the nuclear burst of star formation did not take place) is NGC 502, the farthest from the center of the group of all the galaxies studied.Comment: Slightly edited version of the paper to appear in the Astrophysical Bulletin, 67(3); 24 pages including 8 figure

Childhood growth predicts higher bone mass and greater bone area in early old age : findings among a subgroup of women from the Helsinki Birth Cohort Study

We examined the associations between childhood growth and bone properties among women at early old age. Early growth in height predicted greater bone area and higher bone mineral mass. However, information on growth did not improve prediction of bone properties beyond that predicted by body size at early old age. We examined the associations between body size at birth and childhood growth with bone area, bone mineral content (BMC), and areal bone mineral density (aBMD) in early old age. A subgroup of women (n = 178, mean 60.4 years) from the Helsinki Birth Cohort Study, born 1934-1944, participated in dual-energy X-ray absorptiometry (DXA) measurements of the lumbar spine and hip. Height and weight at 0, 2, 7, and 11 years, obtained from health care records, were reconstructed into conditional variables representing growth velocity independent of earlier growth. Weight was adjusted for corresponding height. Linear regression models were adjusted for multiple confounders. Birth length and growth in height before 7 years of age were positively associated with femoral neck area (p <0.05) and growth in height at all age periods studied with spine bone area (p <0.01). Growth in height before the age of 7 years was associated with BMC in the femoral neck (p <0.01) and birth length and growth in height before the age of 7 years were associated with BMC in the spine (p <0.05). After entering adult height into the models, nearly all associations disappeared. Weight gain during childhood was not associated with bone area or BMC, and aBMD was not associated with early growth. Optimal growth in height in girls is important for obtaining larger skeleton and consequently higher bone mass. However, when predicting bone mineral mass among elderly women, information on early growth does not improve prediction beyond that predicted by current height and weight.Peer reviewe

Limitations of fasting indices in the measurement of insulin sensitivity in Afro-Caribbean adults

In young Afro-Caribbean adults, HOMA-IR compared poorly with other measures of insulin sensitivity. It remains important to determine whether similar findings occur in a more insulin resistant population. However, HOMA-IR correlated with clinical measures of insulin sensitivity (i.e. adiposity), so it may still be useful in epidemiological studies

The duration of embryo culture after mouse IVF differentially affects cardiovascular and metabolic health in male offspring

Study question: Do the long-term health outcomes following IVF differ depending upon the duration of embryo culture before transfer?Summary answer: Using a mouse model, we demonstrate that in male but not female offspring, adverse cardiovascular (CV) health was more likely with prolonged culture to the blastocyst stage, but metabolic dysfunction was more likely if embryo transfer (ET) occurred at the early cleavage stage.What is known already: ART associate with increased risk of adverse CV and metabolic health in offspring, and these findings have been confirmed in animal models in the absence of parental infertility issues. It is unclear which specific ART treatments may cause these risks. There is increasing use of blastocyst, versus cleavage-stage, transfer in clinical ART which does not appear to impair perinatal health of children born, but the longer-term health implications are unknown.Study design, size, duration: Five mouse groups were generated comprising: (i) natural mating (NM)-naturally mated, non-superovulated and undisturbed gestation; (ii) IV-ET-2Cell-in-vivo derived two-cell embryos collected from superovulated mothers, with immediate ET to recipients; (iii) IVF-ET-2Cell-IVF generated embryos, from oocytes from superovulated mothers, cultured to the two-cell stage before ET to recipients; (iv) IV-ET-BL-in-vivo derived blastocysts collected from superovulated mothers, with immediate ET to recipients; (v) IVF-ET-BL-IVF generated embryos, from oocytes from superovulated mothers, cultured to the blastocyst stage before ET to recipients. Both male and female offspring were analysed for growth, CV and metabolic markers of health. There were 8-13 litters generated for each group for analyses; postnatal data were analysed by multilevel random effects regression to take account of between-mother and within-mother variation and litter size.Participants/materials, settings, methods: C57/BL6 female mice (3-4 weeks old) were used for oocyte production; CBA males for sperm with human tubal fluid medium were used for IVF. Embryos were transferred (ET) to MF1 pseudo-pregnant recipients at the two-cell stage or cultured in synthetic oviductal medium enriched with potassium medium to the blastocyst stage before ET. Control in-vivo embryos from C57BL6 × CBA matings were collected and immediately transferred at the two-cell or blastocyst stage. Postnatal assays included growth rate up to 27 weeks; systolic blood pressure (SBP) at 9, 15 and 21 weeks; lung and serum angiotensin-converting enzyme (ACE) activity at time of cull (27 weeks); glucose tolerance test (GTT; 27 weeks); basal glucose and insulin levels (27 weeks); and lipid accumulation in liver cryosections using Oil Red O imaging (27 weeks).Main results and the role of chance: Blastocysts formed by IVF developed at a slower rate and comprised fewer cells that in-vivo generated blastocysts without culture (P < 0.05). Postnatal growth rate was increased in all four experimental treatments compared with NM group (P < 0.05). SBP, serum and lung ACE and heart/body weight were higher in IVF-ET-BL versus IVF-ET-2Cell males (P < 0.05) and higher than in other treatment groups, with SBP and lung ACE positively correlated (P < 0.05). Glucose handling (GTT AUC) was poorer and basal insulin levels were higher in IVF-ET-2Cell males than in IVF-ET-BL (P < 0.05) with the glucose:insulin ratio more negatively correlated with body weight in IVF-ET-2Cell males than in other groups. Liver/body weight and liver lipid droplet diameter and density in IVF-ET-2Cell males were higher than in IVF-ET-BL males (P < 0.05). IVF groups had poorer health characteristics than their in-vivo control groups, indicating that outcomes were not caused specifically by background techniques (superovulation, ET). No consistent health effects from duration of culture were identified in female offspring.Large scale data: N/A.Limitations, reasons for caution: Results from experimental animal models cannot be extrapolated to humans. Nevertheless, they are valuable to develop conceptual models, in this case, in the absence of confounding parental infertility, in assessing the safety of ART manipulations.Wider implications of the findings: The study indicates that longer duration of embryo culture after IVF up to blastocyst before ET leads to increased dysfunction of CV health in males compared with IVF and shorter cleavage-stage ET. However, the metabolic health of male offspring was poorer after shorter versus longer culture duration. This distinction indicates that the origin of CV and metabolic health phenotypes after ART may be different. The poorer metabolic health of males after cleavage-stage ET coincides with embryonic genome activation occurring at the time of ET