scholarly journals 411 Elevated Oxygen Atmospheres as a Decay Control Alternative on Strawberry

HortScience ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 514F-515 ◽  
Author(s):  
Annette L. Wszelaki ◽  
Elizabeth J. Mitcham
Keyword(s):  
Atmospheric Oxygen ◽  
Titratable Acidity ◽  
Soluble Solids ◽  
Postharvest Disease ◽  
Low Oxygen ◽  
Oxygen Levels ◽  
Off Flavors ◽  
Fruit Flavor

Controlled atmospheres have been proven an effective postharvest disease deterrent for strawberries both in transport and storage. However, these treatments do not provide residual protection once the commodity is removed from the atmosphere, and the atmospheres can cause off-flavors in the fruit. Elevated oxygen atmospheres are a novel addition to this technology and could potentially provide better decay control without the harmful effects on fruit flavor aspects. Elevated oxygen will potentially discourage microbial growth, as anaerobes grow best under very low oxygen levels and aerobes grow best under atmospheric oxygen. Threshold elevated oxygen levels to prevent Botrytis cinerea growth in vitro and in vivo on strawberry were assessed. Botrytis cultures (mycelial plugs and spores) and fresh strawberry fruit were exposed to 21%, 40%, 60%, and 80% oxygen atmospheres at 5 °C for 5, 7, and 14 d. Growth of cultures from mycelial plugs was evaluated after treatment and during post-treatment incubation by measuring the diameter of the fungus. Spore germination and germ tube elongation were evaluated every 24 h for 3 days after treatment by counting the number of germinated spores and measuring elongation, respectively. Strawberry quality including firmness, color, soluble solids, titratable acidity, ethylene production and respiration rates, and presence of defects were evaluated upon removal from the elevated oxygen atmospheres as well as after 1, 3, and 5 d storage in air at 20 °C simulating market conditions.

scholarly journals The Role of Tissue Oxygen Tension in Dengue Virus Replication

Cells ◽  
2018 ◽  
Vol 7 (12) ◽  
pp. 241 ◽  
Author(s):  
Efseveia Frakolaki ◽  
Panagiota Kaimou ◽  
Maria Moraiti ◽  
Katerina Kalliampakou ◽  
Kalliopi Karampetsou ◽  
...  
Keyword(s):  
Dengue Virus ◽  
Oxygen Tension ◽  
Atmospheric Oxygen ◽  
Rna Replication ◽  
Metabolic Reprogramming ◽  
Anaerobic Glycolysis ◽  
Low Oxygen ◽  
Hypoxia Response

Low oxygen tension exerts a profound effect on the replication of several DNA and RNA viruses. In vitro propagation of Dengue virus (DENV) has been conventionally studied under atmospheric oxygen levels despite that in vivo, the tissue microenvironment is hypoxic. Here, we compared the efficiency of DENV replication in liver cells, monocytes, and epithelial cells under hypoxic and normoxic conditions, investigated the ability of DENV to induce a hypoxia response and metabolic reprogramming and determined the underlying molecular mechanism. In DENV-infected cells, hypoxia had no effect on virus entry and RNA translation, but enhanced RNA replication. Overexpression and silencing approaches as well as chemical inhibition and energy substrate exchanging experiments showed that hypoxia-mediated enhancement of DENV replication depends on the activation of the key metabolic regulators hypoxia-inducible factors 1α/2α (HIF-1α/2α) and the serine/threonine kinase AKT. Enhanced RNA replication correlates directly with an increase in anaerobic glycolysis producing elevated ATP levels. Additionally, DENV activates HIF and anaerobic glycolysis markers. Finally, reactive oxygen species were shown to contribute, at least in part through HIF, both to the hypoxia-mediated increase of DENV replication and to virus-induced hypoxic reprogramming. These suggest that DENV manipulates hypoxia response and oxygen-dependent metabolic reprogramming for efficient viral replication.

Embryo culture at a reduced oxygen concentration of 5%: a mini review

Zygote ◽  
2019 ◽  
Vol 27 (6) ◽  
pp. 355-361 ◽  
Author(s):  
R. Sciorio ◽  
G.D. Smith
Keyword(s):  
Oxygen Tension ◽  
Embryo Development ◽  
Atmospheric Oxygen ◽  
Embryo Implantation ◽  
Critical Role ◽  
Low Oxygen ◽  
Physiological Level ◽  
Low Oxygen Tension

SummaryThe optimum oxygen tension for culturing mammalian embryos has been widely debated by the scientific community. While several laboratories have moved to using 5% as the value for oxygen tension, the majority of modern in vitro fertilization (IVF) laboratory programmes still use 20%. Several in vivo studies have shown the oxygen tension measured in the oviduct of mammals fluctuates between 2% and 8% and in cows and primates this values drops to <2% in the uterine milieu. In human IVF, a non-physiological level of 20% oxygen has been used in the past. However, several studies have shown that atmospheric oxygen introduces adverse effects to embryo development, not limited to numerous molecular and cellular physiology events. In addition, low oxygen tension plays a critical role in reducing the high level of detrimental reactive oxygen species within cells, influences embryonic gene expression, helps with embryo metabolism of glucose, and enhances embryo development to the blastocyst stage. Collectively, this improves embryo implantation potential. However, clinical studies have yielded contradictory results. In almost all reports, some level of improvement has been identified in embryo development or implantation, without any observed drawbacks. This review article will examine the recent literature and discusses ongoing efforts to understand the benefits that low oxygen tension can bring to mammal embryo development in vitro.

scholarly journals Effect of Low Pressure and Low Oxygen Treatments on Fruit Quality and the In Vivo Growth of Penicillium digitatum and Penicillium italicum in Oranges

Horticulturae ◽  
2021 ◽  
Vol 7 (12) ◽  
pp. 582
Author(s):  
John Archer ◽  
Penta Pristijono ◽  
Quan V. Vuong ◽  
Lluís Palou ◽  
John B. Golding
Keyword(s):  
Fruit Quality ◽  
Titratable Acidity ◽  
Low Pressure ◽  
Fruit Weight ◽  
Penicillium Digitatum ◽  
Soluble Solids ◽  
Low Oxygen ◽  
Exogenous Ethylene ◽  
In Vivo Growth

Penicillium digitatum and P. italicum are the major postharvest pathogens in citrus. To reduce postharvest decay, the use of low-oxygen (0.9 kPa O2) (LO) or low-pressure (6.6 kPa) (LP) treatments were evaluated during the storage of navel oranges for four or eight days. The results showed that exposure to both LO and LP treatments reduced in vivo pathogen growth compared to the untreated (UTC) oranges, with LO being the most effective. The effects of LO and LP on fruit metabolism and quality were further assessed, and it was found that there was no effect on fruit ethylene production, respiration rate, TSS (total soluble solids), TA (titratable acidity) or fruit firmness. However, both LO and LP treatments did have an effect on juice ethanol concentration and fruit weight-loss. The effect of adding exogenous ethylene at either LP (1 µL/L) or atmospheric pressure (AP) (at either 0.1, 1 µL/L) was also evaluated, and results showed that the addition of ethylene at these concentrations had no effect on mould diameter at LP or AP. Therefore, both LO of 0.9 kPa O2 and LP of 6.6 kPa at 20 °C are potential non-chemical postharvest treatments to reduce mould development during storage with minimal effects on fruit quality.

scholarly journals Effect of Alcoholic Extracts of Cymbopogon citratus upon the Control of Colletotrichum gloeosporioides in vitro and upon the Post-harvest Quality of Guavas

2019 ◽  
pp. 1-8
Author(s):  
Ana P. F. A. Santos ◽  
Amanda P. Mattos ◽  
Adriana T. Itako ◽  
João B. Tolentino Júnior ◽  
Gabriela S. Moura ◽  
...  
Keyword(s):  
Colletotrichum Gloeosporioides ◽  
Titratable Acidity ◽  
Physicochemical Characteristics ◽  
Soluble Solids ◽  
Post Harvest ◽  
Methanolic Extracts ◽  
Dose Dependent

Aims: This work aimed at evaluating the effects of ethanolic and methanolic extracts of lemongrass upon the control in vitro of Colletotrichum gloeosporioides and upon the post-harvest quality of guavas “Paluma”. Methodology: We analyzed the inhibition of mycelial growth and sporulation of the pathogen at different concentrations of the extracts (8%; 5%; 3%; 1.5% and 0.5%). In the post-harvest assay, the guavas were treated by immersion in distilled water, ethanolic and methanolic extracts (1%; 0.5% and 0.25%) and stored at 25ºC ± 2ºC for eight days. We evaluated mass loss, total soluble solids, total titratable acidity, ratio, reducing and non-reducing sugars, ascorbic acid and pH and the incidence of anthracnose. Results: In the test in vitro, the pathogen growth inhibition was dose-dependent and the sporulation was completely inhibited upon higher concentrations of extract. At post-harvest, the fruits maintained their physicochemical characteristics, and the treatments were not efficient at retarding fruit ripening. Although the tested treatments inhibited the plant pathogen C. gloesporioides in vitro, they were not efficient at controlling the disease in vivo. Conclusion: The extracts showed control in vitro of C. gloeosporioides at 8%. However, the extracts were not effective at controlling the disease after harvest.

scholarly journals (E)-2-Hexenal Can Stimulate Botrytis cinerea Growth in vitro and on Strawberries in vivo during Storage

1998 ◽  
Vol 123 (5) ◽  
pp. 875-881 ◽  
Author(s):  
Elazar Fallik ◽  
Douglas D. Archbold ◽  
Thomas R. Hamilton-Kemp ◽  
Ann M. Clements ◽  
Randy W. Collins ◽  
...  
Keyword(s):  
Botrytis Cinerea ◽  
Spore Germination ◽  
Mode Of Action ◽  
Mycelial Growth ◽  
Titratable Acidity ◽  
Soluble Solids ◽  
In Vivo Studies ◽  
High Concentration

Some plant-derived natural volatile compounds exhibit antifungal properties and may offer an opportunity to control the causes of postharvest spoilage without affecting quality of, or leaving a residue on, fresh produce. The natural wound volatile (E)-2-hexenal has exhibited significant antifungal activity in earlier studies, but effects on spore germination and mycelial growth have not been separated, nor has the inhibitory mode of action been determined. To determine the efficacy of (E)-2-hexenal for control of Botrytis cinerea Pers. ex Fr. spore germination and mycelial growth, and to examine the mode of action, in vitro and in vivo studies were performed. Under in vitro bioassay conditions, spore germination was more sensitive to the compound than was mycelial growth. Vapor from 10.3 μmol of (E)-2-hexenal in a 120-mL petri dish completely inhibited spore germination. However, 85.6 μmol of (E)-2-hexenal was required to completely inhibit mycelial growth. Lower concentrations of the compound (5.4 and 10.3 μmol) significantly stimulated mycelial growth, especially when the volatile was added 2 days following inoculation. Mycelial growth did not occur as long as the vapor-phase concentration was 0.48 μmol·L-1 or greater. Light microscopy analysis indicated that a high concentration of volatile compound dehydrated fungal hyphae and disrupted their cell walls and membranes. Exposure of B. cinerea-inoculated and non-inoculated strawberry (Fragaria ×ananassa Duch.) fruit in 1.1-L low-density polyethylene film-wrapped containers to vapor of (E)-2-hexenal at 85.6 or 856 μmol (10 or 100 mL, respectively) per container for durations of 1, 4, or 7 days during 7 days of storage at 2 °C promoted the incidence of B. cinerea during subsequent shelf storage at 20 to 22 °C. Loss of fruit fresh mass and fruit firmness during storage at 22 °C was increased by (E)-2-hexenal treatment, but fruit total soluble solids, pH, titratable acidity, and color (L, C, and H values) were not affected. Thus, maintenance of a high vapor-phasel level of (E)-hexenal, perhaps >0.48 μmol·L-1, may be necessary to inhibit mycelial growth and avoid enhancing postharvest mold problems, while significantly higher levels may be necessary to completely eliminate the pathogen.

Oxygen Sensing of Mesenchymal Stem and Progenitor Cells Facilitates Neo-Vasculogenesis In Vivo

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4313-4313
Author(s):  
Nicole A Hofmann ◽  
Andreas Reinisch ◽  
Anna Ortner ◽  
Katharina Schallmoser ◽  
Eva Rohde ◽  
...  
Keyword(s):  
Stem Cell ◽  
Progenitor Cells ◽  
Wound Repair ◽  
Low Oxygen ◽  
Oxygen Levels ◽  
Immune Histochemistry ◽  
Key Factor ◽  
Stem And Progenitor Cells

Abstract Abstract 4313 Background: Vascular homeostasis and regeneration are maintained by proliferating vessel wall-derived somatic endothelial colony-forming progenitor cells (ECFCs). Despite promising experimental data, regenerative stem cell therapy approaches employing ECFCs have been of rather limited efficiency in clinical trials for both therapeutic vasculogenesis as well as anti-angiogenic therapy. We and others have recently shown that ECFC function in vivo requires a stringent interaction with mesenchymal stem and progenitor cells (MSPCs) * [Blood 2009; 113 (26):6716-25]. Co-transplantation of ECFCs and MSPCs is considered to be an advantageous strategy for vascular regenerative medicine. Hypoxia in ischemic tissue is considered to be a key factor influencing pro- and anti-angiogenic treatment by driving the revascularization machinery. In vivo most cells exist under an O2 pressure considerably below air oxygen. In vitro cells are usually expanded under air oxygen and suddenly encounter reduced O2 conditions when re-injected for therapy. Preliminary data suggests that low oxygen conditions differentially regulate stem cell function. We hypothesized that MSPCs act as hypoxia sensors and drive ECFCs to form functioning vessels in vivo. Methods: Adult human ECFCs were isolated and propagated directly from whole venous blood using a novel recovery strategy **[J Vis Exp. 2009;(32) pii: 1524]. MSPCs were isolated from human bone marrow aspirates. During cell culture, pooled human platelet lysate (pHPL) entirely replaced fetal bovine serum. Throughout this study we designated the oxygen level present in vivo in the venous environment as euoxia (41.5±3.4 mmHg). Oxygen levels below euoxia are defined as hypoxia (27.4±7.3 mmHg). Air-oxygen commonly used in standard laboratory practice is above euoxia and is therefore referred to as hyperoxia (139.8±2.9 mmHg). Progenitor cell phenotype, hierarchy, long-term proliferation, wound repair as well as migratory and vasculogenic functions were monitored under euoxia as compared to hypoxic or hyperoxic conditions. Molecular regulation of cellular responses to different oxygen levels was assessed by flow cytometry, immune cytochemistry and proteomic profiling. ECFC and MSPC interactions in vivo were studied in immune-deficient NSG mice (NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ) after sub-cutaneous co-implantation in matrigel plugs. Immune histochemistry and TUNEL assays were performed on plugs at day 1, 7 and 14 after transplantation. Results: Compared to hyperoxic standard laboratory conditions in vitro, proliferation of ECFCs and MSPCs in primary and long-term cultures was significantly reduced under euoxia, and even more under hypoxic conditions. Hyperoxic conditioning resulted in a shift in progenitor hierarchy with an augmented number of ECFC high proliferative potential (HPP) colonies (60±18% of total colonies) as compared to euoxia (9±6%) and a complete loss of HPP colonies under hypoxia (0%). The absolute colony number remained unchanged independent of oxygen levels. Both ECFC vascular wound repair in scratch assays and matrigel vascular-like network formation in vitro were improved with escalating oxygen supply. The reoxygenation of hypoxic and euoxic ECFCs led to enhanced proliferation and function. Furthermore, MSPCs stabilized hypoxia inducible factor-1α (HIF-1α) under hypoxic as well as euoxic conditions, whereas ECFCs only stabilized HIF-1α when confronted with hypoxia in vitro. In a mouse model, subcutaneously injected ECFCs in matrigel underwent apoptosis after 1 day and attracted mouse leucocytes which infiltrated the matrigel plug. Co-implantation of ECFCs and MSPCs in these matrigel plugs resulted in reduced apoptosis and formation of perfused human vessels as soon as 7 days after transplantation. In this in vivo setting, perivascular cells but not endothelial cells were positive for HIF-1α in immune histochemistry. Background: These data indicate that oxygen levels differentially regulate ECFC and MSPC function during vascular homeostasis and regeneration. While hypoxic ECFCs alone are not able to function in vitro and form patent vessels in vivo, MSPCs react to the low oxygen environment and support ECFCs to perform vessel formation in vivo at least in part by rescuing ECFCs from hypoxia-induced apoptosis. This suggests that oxygen appears to be a key factor in stem cell transplantation and regenerative medicine. Disclosures: No relevant conflicts of interest to declare.

scholarly journals High CO2 Storage Improves the Shelf Life of `Arapaho' and `Navaho' Blackberries

HortScience ◽  
2000 ◽  
Vol 35 (4) ◽  
pp. 556C-556b
Author(s):  
P. Perkins-Veazie ◽  
J.K. Collins
Keyword(s):  
Shelf Life ◽  
Co2 Storage ◽  
Titratable Acidity ◽  
Soluble Solids ◽  
Anthocyanin Content ◽  
Low Oxygen ◽  
Off Flavors ◽  
Solids Content ◽  
Atmosphere Storage ◽  
Treatment Application

Application of modified-atmosphere storage (MA) (high carbon dioxide and/or low oxygen) extends the shelf life of several fruits. This study was done to determine the effects of MA on quality and flavor of blackberries. `Navaho' and `Arapaho' blackberries were harvested in 1998 and 1999, precooled overnight at 2 °C, and placed in 0.5-L treatment jars. Treatments of 15% CO2/10% O2 or of air (0.03% CO2/21% O2) were applied at 2 °C for 3, 7, or 14 days. After treatment application, jars were held at 2 °C for an additional 11, 7, or 0 days, respectively. Seven and 14 days of application of CO2 reduced the incidence of decayed and leaky berries by 10% to 20% for both `Arapaho' and `Navaho', but firm berries decreased 10% after 14 days of treatment. Titratable acidity was slightly lower, and pH higher, in control fruit but soluble solids content was not affected by treatment. Anthocyanin content was not affected by treatment in `Arapaho' berries but was lower in `Navaho' berries after 7 and 14 days of treatment. Samples taken for taste tests after 3 and 7 days of treatment had no off-odors or off-flavors. `Arapaho' and `Navaho' blackberries benefitted from high CO2 storage, with a minimum of 7 days of treatment application needed to increase marketable berries by 10%.

scholarly journals Acibenzolar-S-methyl against Botrytis mold on table grapes in vitro and in vivo

2019 ◽  
Vol 5 (1) ◽  
pp. 52 ◽  
Author(s):  
Khamis Youssef ◽  
Sergio Roberto ◽  
Ronan Colombo ◽  
Marcelo Canteri ◽  
Kamel Elsalam
Keyword(s):  
Mycelial Growth ◽  
Titratable Acidity ◽  
Gray Mold ◽  
Soluble Solids ◽  
Table Grapes ◽  
Significant Difference ◽  
Randomized Experimental Design ◽  
Set Up

The objective of this work was to investigate the effect of the resistance inducer Acibenzolar-S-methyl (ASM), against Botrytis mold on table grapes in vitro and in vivo. To assess the effect of ASM on mycelial growth Botrytis cinerea, different concentrations (0.125, 0.25, 0.5, 1.0, 2.0 and 3% w:v) were tested. Treatments were set up in triplicate, in a completely randomized experimental design, and replicated twice. Results were expressed in minimum inhibitory concentrations and effective dose per 50% response of mycelial growth. Healthy table grapes (cvs. Italia and Benitaka) were harvested at full ripe to evaluate the ASM 1% effect against gray mold under artificial conditions. Bunches were split into two groups in order to perform two types of experiments (spray or immersion). For both trials, treated bunches were arranged in carton boxes and stored at 2±1 °C, for one month, followed by one week of shelf-life at 22±2 °C. In order to evaluate the ASM effect against gray mold under field conditions, ASM 1% was sprayed on both cultivars one week before harvest. Grapes treated with iprodione 0.2% with three applications during the season were included as a standard chemical control. Bunches were harvested at full ripe, arranged in carton boxes and submitted to a cold storage process as described previously. Results for the in vitro experiments showed that the minimum inhibitory concentration of ASM was achieved by 3% and the ED50 was 0.04%. Under artificial conditions, for both cultivars, the efficacy of ASM was higher when the grapes were immersed than sprayed. A significant difference was observed for ASM as compared with control. Regarding the effect of ASM against gray mold in the field, the incidence of gray mold was recorded for both cultivars. For ‘Italia’ and ‘Benitaka’ grapes, ASM, iprodione and sulfur dioxide pad reduced the incidence of gray mold by 85, 79 and 77%, and by 80.5, 73 and 82%, respectively. As for the physico-chemical berry properties, none of the treatments were significantly different from the control for total soluble solids, titratable acidity and color index. A single ASM treatment applied one week before harvest is effective for controlling gray mold in ‘Italia’ and ‘Benitaka’ table grapes.

scholarly journals Use of phosphites in postharvest to control anthracnose of yellow passionfruit

2019 ◽  
Vol 35 (6) ◽  
Author(s):  
Jaqueline Barbosa Dutra ◽  
Luiz Eduardo Bassay Blum
Keyword(s):  
Titratable Acidity ◽  
Soluble Solids ◽  
Alternative Methods ◽  
Postharvest Diseases ◽  
Passiflora Edulis ◽  
Physico Chemical ◽  
Colletotrichum Spp ◽  
Production Problems

Brazil is the largest producer of yellow passionfruit (Passiflora edulis f. flavicarpa) and one of its production problems is the anthracnose (Colletotrichum spp.). The use of fungicides on control of postharvest diseases is a method that protects the fruits during storage. However, precautions must be taken due to fungicide toxicity. The restriction to the use of fungicides in post-harvest led a demand for alternative methods of disease control, and, the phosphite application is one of these methods. Therefore, this work aimed to evaluate the effects of fruit immersion in phosphite on postharvest control of anthracnose. Two tests were developed in vitro to assess the effect on the fungus: phosphite Mg2 (40%P2O5+6%Mg), Zn (40%P2O5+10%Zn), Ca1 (30%P2O5+7%Ca) and K1 (40%P2O5+20%K2O). For the in vivo tests, passionfruit (Gigante Amarelo), were wounded and inoculated (50mL; 106conidia mL-1). Two tests were done with: Cu (25%P2O5+5%Cu), 2.5mL L-1; Zn, 2.5mL L-1; K1, 2.5mL L-1; Mg1 (30%P2O5+4%Mg), 3mL L-1; Ca1, 3mL L-1; Ca2 (10%P2O5+6%Ca), 4mL L-1; K2 (40%P2O5+20%K2O), 1.5mL L-1; Mg2 (40%P2O5+6%Mg), 1.5mL L-1; K3 (20%P2O5+20%K2O) 1.75 mL L-1; K4 (30%P2O5+20%K2O), 1.75mL L-1. Other two tests with phosphites Mg2, Ca1, Zn and K1 were with CaCl2 (2%) was developed. In addition, phosphites were tested at 25, 50, 100 and 200% of the dose: K2 (100%; 1.5mL L-1) and Ca1 (100%; 3 mL L-1). The phosphites Mg2, Ca1, K1 and Zn in vitro have reduced mycelial growth and fungus conidia production. The phosphites K1, K2, Ca1 and Zn were the ones that most reduced the size of the anthracnose lesion. There were no differences among treatments, concerning the physico-chemical fruit properties analyzed (% fresh mass loss, total soluble solids, pH and titratable acidity).

INFLUENCE OF OXYGEN TENSION ON SOMATOMEDIN ACTIVITY IN VITRO

1977 ◽  
Vol 72 (3) ◽  
pp. 361-369 ◽  
Author(s):  
JENNIFER M. DEHNEL ◽  
D. L. HAMBLEN
Keyword(s):  
Growth Plate ◽  
Oxygen Tension ◽  
Atmospheric Oxygen ◽  
Calf Serum ◽  
Growth Patterns ◽  
Foetal Calf Serum ◽  
Low Oxygen ◽  
Epiphyseal Growth Plate

SUMMARY Somatomedins are the intermediaries through which growth hormone acts on the epiphyseal growth plate to effect linear skeletal growth. Rat epiphyseal chondrocytes were isolated and cultured in vitro in the presence of somatomedin. Two sources of somatomedin were used, foetal calf serum and rat liver perfusates. The chondrocytes proliferated and synthesized sulphated glycosaminoglycans when grown in the presence of somatomedin from either source, but were not metabolically active in chemically defined medium alone. Some differences in the growth patterns in response to serum or liver somatomedins are reported and discussed. Chondrocyte metabolic activity in the presence of somatomedin in vitro showed a graded response to alterations in the atmospheric oxygen, being greatest at low oxygen pressure, and almost completely inhibited at 95% oxygen. A gradient of local oxygen tension has been reported to exist across the epiphyseal plate in vivo. The effects of somatomedin combined with changing oxygen levels may help to explain the divergence of cell proliferation and matrix synthesis seen in the various regions of the growth plate.

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