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  • Oxford University Press (OUP)  (5)
  • 1
    In: Journal of Animal Science, Oxford University Press (OUP), Vol. 101 ( 2023-01-03)
    Abstract: This experiment was conducted to determine the effects of yeast-derived postbiotic (YDP) supplementation in sow diets during late gestation and lactation on the performance of sows and their offspring. At 90-d gestation, 150 sows (Landrace × Large White, parity: 3.93 ± 0.11) were allocated to three dietary treatments (n = 50 per treatment): 1) basal diet (control [CON]), 2) basal diet with 1.25 g/kg YDP (0.125 group), and 3) basal diet with 2.00 g/kg YDP (0.200 group). The experiment continued until the end of weaning (day 21 of lactation). Supplementation with YDP resulted in greater deposition of backfat in sows during late gestation and an increasing trend in average weaning weight of piglets than observed in the CON group (P  & lt; 0.01, P = 0.05). Supplementation with YDP decreased piglet mortality and diarrhea index in piglets (P  & lt; 0.05). In farrowing sows’ serum, the glutathione peroxide content in the YDP group was lower than that in the CON group (P  & lt; 0.05); the content of immunoglobulin A (IgA) in the 0.200 group or YDP group was higher than that in the CON group (P  & lt; 0.05). In lactating sows’ serum, malondialdehyde content was higher in the YDP group (P  & lt; 0.05). In day 3 milk of sows, the 0.200 group tended to increase the lactose content (P = 0.07), and tended to decrease the secretory immunoglobulin A (sIgA) content (P = 0.06) with respect to that in the CON group. The sIgA content in the YDP group was lower than that in the CON group (P  & lt; 0.05). In the milk of sows, the 0.200 group tended to increase the lactose content with respect to that in the CON group (P = 0.08); the immunoglobulin G (IgG) content in the 0.125 group or YDP group was higher than that in the CON group (P  & lt; 0.05). YDP supplementation increased the IgA content in the milk (P  & lt; 0.01). In sow placenta, the content of total anti-oxidant capacity in the YDP group was higher than that in the CON group (P = 0.05); and the content of transforming growth factor-β in the YDP group was higher than that in the CON group (P  & lt; 0.05). In piglet serum, the content of IgG and immunoglobulin M in the 0.125 group was higher than that in the CON and 0.200 groups (P  & lt; 0.05). In summary, this study indicated that feeding sows diets supplemented with YDP from late gestation through lactation increased sows’ backfat deposition in late gestation and piglets’ weaning weight; decreased piglet mortality and diarrhea index in piglets; and improved maternal and offspring immunity.
    Type of Medium: Online Resource
    ISSN: 0021-8812 , 1525-3163
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2023
    detail.hit.zdb_id: 1490550-4
    SSG: 12
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  • 2
    In: Protein & Cell, Oxford University Press (OUP), Vol. 7, No. 11 ( 2016-11), p. 804-819
    Type of Medium: Online Resource
    ISSN: 1674-800X , 1674-8018
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2016
    detail.hit.zdb_id: 2543451-2
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  • 3
    In: Rheumatology, Oxford University Press (OUP), Vol. 61, No. Supplement_1 ( 2022-04-23)
    Abstract: High-resolution peripheral quantitative computed tomography (HR-pQCT) scanning provides such detailed, 3-dimensional reconstructions of the skeleton that the images have been called ‘a virtual bone biopsy’. Traditional analysis of the images results in a multitude of cortical and trabecular parameters which would be potentially cumbersome to interpret for clinicians compared to user-friendly tools such as FRAX®. A computer vision approach, where the entire scan is ‘read’ by a computer algorithm to ascertain fracture risk, would be far simpler. Thus, we investigated whether a computer vision and machine learning technique could improve the current methods of assessing fracture risk. Methods This study was nested in the Hertfordshire Cohort Study, a group of community-dwelling older adults. Participants attended research visits at which height and weight were measured; fracture history was determined via self-report and vertebral fracture assessment. Bone microarchitecture was assessed via HR-pQCT scans of the non-dominant distal tibia (Scanco XtremeCT) and bone mineral density measurement and lateral vertebral assessment were performed using dual X-ray absorptiometry (DXA) (Lunar Prodigy Advanced). Images were cropped and pre-processed and texture analysis was performed using a 3-dimensional local binary patterns method. These analyses, together with age, sex, height, weight, BMI, and dietary calcium, were used in the random-forest classification algorithm. Receiver operating characteristic (ROC) analysis was used to compare fracture risk identification methods. Results Overall, 247 males and 149 females were included in this study with a mean age of approximately 76 years. Using clinical risk factors alone gave an area under the curve (AUC) of 0.70 (95% CI: 0.56-0.84), which improved to 0.71 (0.57-0.85) with the addition of DXA-measured BMD. The addition of the machine learning classifier to clinical risk factors and DXA-measured BMD lead to an improved AUC of 0.90 (0.83-0.96) with a sensitivity of 0.83 and specificity of 0.74. Conclusion The results of this preliminary work demonstrate that using a 3-dimensional computer vision method to HR-pQCT scanning can enhance the identification of those at risk of fracture beyond that afforded by clinical risk factors and DXA-measured BMD. This approach has the potential to make the information offered by HR-pQCT more accessible and applicable to healthcare professionals in the clinic if the technology becomes more widely available. Whilst these findings require replication in other cohorts, they are an early indicator that the application of a machine learning technique to bone microarchitecture could improve fracture prediction and osteoporosis care. Disclosure N.R. Fuggle: None. S. Lu: None. M. Ó Breasail: None. L.D. Westbury: None. K.A. Ward: None. E. Dennison: None. S. Mahmoodi: None. M. Niranjan: None. C. Cooper: None.
    Type of Medium: Online Resource
    ISSN: 1462-0324 , 1462-0332
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2022
    detail.hit.zdb_id: 1474143-X
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  • 4
    In: Biology of Reproduction, Oxford University Press (OUP), Vol. 104, No. 6 ( 2021-06-04), p. 1322-1336
    Abstract: Leydig cells play a critical role in male reproductive physiology, and their dysfunction is usually associated with male infertility. Melatonin has an important protective and regulatory role in these cells. However, the lack of suitable animal models impedes us from addressing the impact of endogenous melatonin on these cells. In the current study, by using arylalkylamine N-acetyltransferase (AANAT) overexpression transgenic sheep and AANAT knockout mice, we confirmed the regulatory effects of endogenously occurring melatonin on Leydig cells as well as its beneficial effects on male reproductive performance. The results showed that the endogenously elevated melatonin level was correlated with decreased Leydig cell apoptosis, increased testosterone production, and improved quality of sperm in melatonin-enriched transgenic mammals. Signal transduction analysis indicated that melatonin targeted the mitochondrial apoptotic Bax/Bcl2 pathway and thus suppressed Leydig cell apoptosis. In addition, melatonin upregulated the expression of testosterone synthesis-related genes of Steroidogenic Acute Regulatory Protein (StAR), Steroidogenic factor 1 (SF1), and Transcription factor GATA-4 (Gata4) in Leydig cells. This action was primarily mediated by the melatonin nuclear receptor RAR-related orphan receptor alpha (RORα) since blockade of this receptor suppressed the effect of melatonin on testosterone synthesis. All of these actions of melatonin cause Leydig cells to generate more testosterone, which is necessary for spermatogenesis in mammals. In contrast, AANAT knockout animals have dysfunctional Leydig cells and reduced reproductive performance.
    Type of Medium: Online Resource
    ISSN: 0006-3363 , 1529-7268
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2021
    detail.hit.zdb_id: 1469812-2
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2023
    In:  Biometrika Vol. 110, No. 2 ( 2023-05-15), p. 449-465
    In: Biometrika, Oxford University Press (OUP), Vol. 110, No. 2 ( 2023-05-15), p. 449-465
    Abstract: For the case with a single causal variable, Dawid et al. (2014) defined the probability of causation, and Pearl (2000) defined the probability of necessity to assess the causes of effects. For a case with multiple causes that could affect each other, this paper defines the posterior total and direct causal effects based on the evidence observed for post-treatment variables, which could be viewed as measurements of causes of effects. Posterior causal effects involve the probabilities of counterfactual variables. Thus, as with the probability of causation, the probability of necessity and direct causal effects, the identifiability of posterior total and direct causal effects requires more assumptions than the identifiability of traditional causal effects conditional on pre-treatment variables. We present assumptions required for the identifiability of posterior causal effects and provide identification equations. Further, when the causal relationships between multiple causes and an endpoint can be depicted by causal networks, we can simplify both the required assumptions and the identification equations of the posterior total and direct causal effects. Finally, using numerical examples, we compare the posterior total and direct causal effects with other measures for evaluating the causes of effects and the population attributable risks.
    Type of Medium: Online Resource
    ISSN: 0006-3444 , 1464-3510
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    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2023
    detail.hit.zdb_id: 1119-8
    detail.hit.zdb_id: 1470319-1
    SSG: 12
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