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Institution

University of Stirling

EducationStirling, Stirling, United Kingdom
About: University of Stirling is a education organization based out in Stirling, Stirling, United Kingdom. It is known for research contribution in the topics: Population & Polyunsaturated fatty acid. The organization has 7722 authors who have published 20549 publications receiving 732940 citations. The organization is also known as: Stirling University.


Papers
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Journal ArticleDOI
TL;DR: The results establish that the formation of 22: 6(n - 3) in hepatocytes of rainbow trout is stimulated by omitting 22:6(n- 3) from the diet and are consistent with the biosynthesis of 24:5(n)-3) and 24:6 (n-3) in trout liver cells proceeding via 24:4(n) and 25:4 (n -3) intermediates.

186 citations

Book ChapterDOI
01 Jan 2009
TL;DR: The present chapter describes the biochemistry and molecular biology involved in the various pathways of PUFA biosynthesis and interconversions in aquatic ecosystems.
Abstract: It is now well established that the long-chain, omega-3 (ω3 or n-3) polyunsaturated fatty acids (PUFA) are vitally important in human nutrition, reflecting their particular roles in critical physiological processes (see Chap 14) In comparison to terrestrial ecosystems, marine or freshwater ecosystems are characterised by relatively high levels of long-chain n-3PUFA and, indeed, fish are the most important source of these vital nutrients in the human food basket Virtually all PUFA originate from primary producers but can be modified as they pass up the food chain This is generally termed trophic upgrading, and various aspects of these phenomena have been described in Chaps 2, 6 and 7 (this volume) However, while qualitative aspects of essential fatty acid production and requirements in aquatic ecosystems are relatively well understood, in order to fully understand and model ecosystems, quantitative information is needed on synthesis and turnover rates of n-3PUFA at different trophic levels in the food web The present chapter describes the biochemistry and molecular biology involved in the various pathways of PUFA biosynthesis and interconversions in aquatic ecosystems

186 citations

Journal ArticleDOI
TL;DR: In this paper, it is shown that in eutrophic lakes, the subsequent dominance by phytoplankton is more likely to be a result of the loss of vegetation rather than the cause, and the longer-term stability of macrophyte dominance is also reduced if there are few surviving plant species.

186 citations

Journal ArticleDOI
TL;DR: A novel mechanism for the training‐induced improvements in IMTG breakdown and insulin sensitivity is suggested, and it is shown that SIT is an alternative, time‐efficient training strategy that induces similar beneficial metabolic adaptations.
Abstract: Intramuscular triglyceride (IMTG) utilization is enhanced by endurance training (ET) and is linked to improved insulin sensitivity. This study first investigated the hypothesis that ET-induced increases in net IMTG breakdown and insulin sensitivity are related to increased expression of perilipin 2 (PLIN2) and perilipin 5 (PLIN5). Second, we hypothesized that sprint interval training (SIT) also promotes increases in IMTG utilization and insulin sensitivity. Sixteen sedentary males performed 6 weeks of either SIT (4-6, 30 s Wingate tests per session, 3 days week(-1)) or ET (40-60 min moderate-intensity cycling, 5 days week(-1)). Training increased resting IMTG content (SIT 1.7-fold, ET 2.4-fold; P < 0.05), concomitant with parallel increases in PLIN2 (SIT 2.3-fold, ET 2.8-fold; P < 0.01) and PLIN5 expression (SIT 2.2-fold, ET 3.1-fold; P < 0.01). Pre-training, 60 min cycling at ∼65% pre-training decreased IMTG content in type I fibres (SIT 17 ± 10%, ET 15 ± 12%; P < 0.05). Following training, a significantly greater breakdown of IMTG in type I fibres occurred during exercise (SIT 27 ± 13%, ET 43 ± 6%; P < 0.05), with preferential breakdown of PLIN2- and particularly PLIN5-associated lipid droplets. Training increased the Matsuda insulin sensitivity index (SIT 56 ± 15%, ET 29 ± 12%; main effect P < 0.05). No training × group interactions were observed for any variables. In conclusion, SIT and ET both increase net IMTG breakdown during exercise and increase in PLIN2 and PLIN5 protein expression. The data are consistent with the hypothesis that increases in PLIN2 and PLIN5 are related to the mechanisms that promote increased IMTG utilization during exercise and improve insulin sensitivity following 6 weeks of SIT and ET.

186 citations

Journal ArticleDOI
TL;DR: ASyMS has the potential to positively impact on the management of symptoms in patients receiving chemotherapy treatment and patients' perceptions of ASyMS were evaluated pre and post participation.
Abstract: Chemotherapy forms a core component of treatment for the majority patients with cancer Recent changes in cancer services mean patients frequently receive such treatment as outpatients and are often required to manage side effects at home without direct support from oncology health professionals Information technology continues to develop to support patients in the community; this study evaluated the impact of a mobile phone-based advanced symptom management system (ASyMS) on chemotherapy related toxicity in patients with lung, breast or colorectal cancer One hundred and twelve patients were randomized from seven clinical sites across the UK; 56 patients used the mobile phone to record their symptoms, sending their reports directly to the nurses at their clinical site; 56 control group patients received standard care Health professionals were alerted about any severe or life-threatening symptoms through the development of a chemotherapy symptom risk model Patients' perceptions of ASyMS were evaluated pre and post participation Patients reported many benefits of using ASyMS including improved communication with health professionals, improvements in the management of their symptoms, and feeling reassured their symptoms were being monitored while at home ASyMS has the potential to positively impact on the management of symptoms in patients receiving chemotherapy treatment

186 citations


Authors

Showing all 7824 results

NameH-indexPapersCitations
Paul M. Thompson1832271146736
Alan D. Baddeley13746789497
Wolf Singer12458072591
John J. McGrath120791124804
Richard J. Simpson11385059378
David I. Perrett11035045878
Simon P. Driver10945546299
David J. Williams107206062440
Linqing Wen10741270794
John A. Raven10655544382
David Coward10340067118
Stuart J. H. Biddle10248441251
Malcolm T. McCulloch10037136914
Andrew P. Dobson9832244211
Lister Staveley-Smith9559936924
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202357
2022175
20211,041
20201,054
2019916
2018903