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急性胰腺炎犬外周氧化应激生物标志物。

Peripheral biomarkers of oxidative stress in dogs with acute pancreatitis.

机构信息

Department of Small Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, Michigan, USA.

Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, Michigan, USA.

出版信息

J Vet Intern Med. 2022 Nov;36(6):1958-1965. doi: 10.1111/jvim.16535. Epub 2022 Sep 10.

DOI:10.1111/jvim.16535
PMID:36086902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9708408/
Abstract

BACKGROUND

Oxidative stress is considered a pathomechanism of acute pancreatitis (AP), but no studies have extensively characterized oxidant status in dogs with naturally-occurring AP.

HYPOTHESIS OR OBJECTIVES

Evaluate measures of oxidant status in dogs with AP and explore whether these measures correlate with AP severity.

ANIMALS

Fifteen dogs with AP and 9 control dogs.

METHODS

Prospective, controlled observational study. Plasma reactive metabolite (RM) concentrations, antioxidant potential (AOP), and urinary F isoprostane concentrations were measured in AP dogs and healthy controls. Severity of AP was assessed by length of hospitalization and 3 disease severity indices: canine acute pancreatitis severity (CAPS), modified canine activity index (M-CAI), and the acute patient physiologic and laboratory evaluation score (APPLE ).

RESULTS

Reactive metabolite (RM) concentrations (median, 65 relative fluorescent units [RFU]/μL; range, 20-331 RFU/μL) and RM:AOP (median, 7; range, 4-109) were higher in AP dogs than healthy controls (median RM, 25 RFU/μL; range, 16-41 RFU/μL; median RM:AOP, 4; range, 2-7; P < .001 for both comparisons). Reactive metabolite (r  = 0.603, P = .08) and RM:AOP (r  = 0.491, P = .06) were not correlated with the duration of hospitalization or disease severity indices evaluated. However, disease severity indices did not predict mortality in our study. Normalized urine 2,3-dinor-8-iso-prostaglandin F2α concentrations were correlated with C-reactive protein (CRP; r  = 0.491, P = .03), canine specific pancreatic lipase (Spec cPL; r  = 0.746, P = .002), and CAPS (r  = 0.603, P = .02).

CONCLUSIONS AND CLINICAL IMPORTANCE

Oxidant status is altered in dogs with naturally occurring AP, but the clinical relevance of this finding is unknown.

摘要

背景

氧化应激被认为是急性胰腺炎(AP)的一种发病机制,但尚无研究广泛描述患有自发性 AP 的犬的氧化剂状态。

假设或目的

评估患有 AP 的犬的氧化剂状态,并探讨这些措施是否与 AP 的严重程度相关。

动物

15 只患有 AP 的犬和 9 只对照犬。

方法

前瞻性、对照观察性研究。测量患有 AP 的犬和健康对照犬的血浆反应代谢产物(RM)浓度、抗氧化能力(AOP)和尿 F 异前列烷浓度。通过住院时间和 3 种疾病严重程度指数评估 AP 的严重程度:犬急性胰腺炎严重程度(CAPS)、改良犬活动指数(M-CAI)和急性患者生理和实验室评估评分(APPLE)。

结果

反应代谢产物(RM)浓度(中位数,65 相对荧光单位[RFU]/μL;范围,20-331 RFU/μL)和 RM:AOP(中位数,7;范围,4-109)在 AP 犬中均高于健康对照组(中位数 RM,25 RFU/μL;范围,16-41 RFU/μL;中位数 RM:AOP,4;范围,2-7;两者比较 P < .001)。RM(r = 0.603,P = 0.08)和 RM:AOP(r = 0.491,P = 0.06)与住院时间或评估的疾病严重程度指数均无相关性。然而,在我们的研究中,疾病严重程度指数并不能预测死亡率。尿液 2,3-二去-8-异前列腺素 F2α浓度与 C 反应蛋白(CRP;r = 0.491,P = 0.03)、犬特异性胰脂肪酶(Spec cPL;r = 0.746,P = 0.002)和 CAPS(r = 0.603,P = 0.02)呈正相关。

结论和临床意义

患有自发性 AP 的犬的氧化应激状态发生改变,但这一发现的临床意义尚不清楚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361a/9708408/1e06f9862b09/JVIM-36-1958-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361a/9708408/1e06f9862b09/JVIM-36-1958-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/361a/9708408/1e06f9862b09/JVIM-36-1958-g001.jpg

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本文引用的文献

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Advances in the diagnosis of acute pancreatitis in dogs.犬急性胰腺炎诊断的进展
J Vet Intern Med. 2021 Nov;35(6):2572-2587. doi: 10.1111/jvim.16292. Epub 2021 Nov 9.
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Serum concentrations of canine pancreatic lipase immunoreactivity and C-reactive protein for monitoring disease progression in dogs with acute pancreatitis.
血清犬胰脂肪酶免疫活性和 C 反应蛋白浓度监测急性胰腺炎犬疾病进展。
J Vet Intern Med. 2021 Sep;35(5):2187-2195. doi: 10.1111/jvim.16218. Epub 2021 Jul 11.
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J Small Anim Pract. 2021 Oct;62(10):866-873. doi: 10.1111/jsap.13361. Epub 2021 May 24.
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Dietary patterns and biomarkers of oxidative stress and inflammation: A systematic review of observational and intervention studies.饮食模式与氧化应激和炎症生物标志物:观察性和干预性研究的系统综述。
Redox Biol. 2021 Jun;42:101869. doi: 10.1016/j.redox.2021.101869. Epub 2021 Jan 22.
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Antioxidants (Basel). 2021 Jan 20;10(2):145. doi: 10.3390/antiox10020145.
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