Serial measurements of Paraoxonase-1 (PON-1) activity in horses with experimentally induced endotoxemia

doi:10.21203/rs.3.rs-61750/v2

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Serial measurements of Paraoxonase-1 (PON-1) activity in horses with experimentally induced endotoxemia

https://doi.org/10.21203/rs.3.rs-61750/v2

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published 04 Nov, 2020

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Background: Paraoxonase-1 (PON-1) is an antioxidant enzyme, whose activity decreases during the acute phase response in many species. Little is known about PON-1 and its role as a negative acute phase protein during septic inflammation in horses, but promising findings about its utility in diagnosing SIRS and predicting the outcome in diseased horses, were recently highlighted. The objective of the study was to investigate the behaviour of PON-1 in horses after experimentally induced endotoxemia. To this aim, PON-1 activity was measured on 66 plasma samples collected from six clinically healthy mares, previously included in another study, before and at multiple time points between 12 and 240 hours after intravenous infusion of Escherichia coli O55:B5 lipopolysaccharide (LPS).

Results: compared with baseline values, a progressive transient decrease of PON-1 activity was observed starting from 24 hours post-infusion, with lowest values observed between 3 to 7 days post-infusion, followed by a normalisation to pre-infusion levels the tenth day.

Conclusions: the results of this study suggest that measurement and monitoring of PON-1 activity might be useful to evaluate progression and recovery from endotoxemia in horses. Further studies in horses with naturally occurring sepsis are warranted.

Large Animal Medicine

equine

inflammation

oxidative stress

Paraoxonase-1 (PON-1) was the first discovered and the most studied of the three members of the mammalian paraoxonases family (1,2). This enzyme, with esterase and lactonase activities, is mainly synthesized in the liver, circulates in blood bound to high-density lipoproteins (HDL) (3) and protects low-density and high-density lipoproteins from oxidation by hydrolysing oxidized lipids (4–8). PON-1 is therefore considered an antioxidant enzyme, but also a modulator of the inflammatory response (9) and part of the immune system (10). In the last year’s research, there has been growing interest about the role of PON-1 in the pathogenesis of many diseases characterized by oxidative stress, primarily in human medicine (11,12), but more recently also in veterinary medicine. In particular, several studies have highlighted the potential of PON-1 in the pathogenesis, diagnosis and prediction of outcome in naturally occurring and experimentally induced sepsis in many species, including horses (13–25). During the acute phase response, changes in lipoprotein occur (26) and PON-1 in HDL is replaced by acute phase proteins, mainly serum amyloid A. Together with down-regulation of hepatic PON-1 gene expression, these changes cause a decrease in its activity (27), which appears to be more pronounced when inflammation is associated to infection (10) and when inflammation is more severe (16). A recent study validated a paraoxon-based method to measure serum PON-1 activity in horses and provided reference intervals in healthy animals for this species (28). Interestingly, in a further study, low PON-1 activity was reported only in some of the horses with systemic inflammatory response syndrome (SIRS) (15). Therefore, although the latter study indicated that low PON-1 activity at admission may predict the presence of SIRS or a poor outcome, to date very little is known about PON-1 in horses, and additional information is required to confirm that this protein could have a diagnostic or prognostic marker, as reported for other species. The aim of the study was to investigate the behaviour of plasma PON-1 activity from horses with experimentally induced endotoxemia included in a previous study, on which the administration of LPS induced evident haematological and biochemical changes consistent with inflammation. The hypothesis of the study was that oxidative phenomena associated with endotoxemia may induce a decrease of PON-1 activity that parallels the other changes detected after LPS administration.

Table 1 and Figure 1 report PON-1 activity measured at scheduled time points. A progressive decrease in PON-1 activity from baseline was observed from 24 hours after the end of LPS infusion.

Table 1

Blood sampling time (hours)	PON-1 activity (U/mL)
Blood sampling time (hours)	Mean ± S.D.	Median	Min-Max range
0	33.7 ± 6.3	35.6	28.8-38.4
2	34.6 ± 8.2	31.5	30.0-42.7
6	33.0 ± 7.9	31.7	27.3-36.5
12	33.5 ± 5.4	33.3	29.1-36.4
24	31.9 ± 8.8	33.1	22.5-39.7
36	27.6 ± 5.8	28,8	23.4-32.6
48	27.2 ± 5.8	27.5	22,2-32,3
72	23.5 ± 6.4	24.6	16.4-29.2
168	24.8 ± 5.3	24,5	20.9-29.7
240	30.6 ± 5.1	32.4	24.5-34.5

Mean, standard deviation, median and range of plasma PON-1 activity for scheduled time points before (T0) and after (T2-T240) LPS administration in healthy horses (n=6). Asterisks indicate values significantly different (P<0.05) from reported time points.

The Friedmann test evidenced that results collected at the different sampling times were significantly different to each other (P<0.001). Mean PON-1 values measured from 48 hours to 168 hours post-infusion were significantly lower than those recorded in the samples collected in the first 24 hours and especially from the baseline values. After this transient decrease, at 240 hours post-infusion PON-1 activity returned to similar baseline values, significantly higher than lowest ones observed 72- and 168-hours post-infusion. Moreover, PON-1 activity was negatively correlated with fibrinogen (P<0.001, rs= -0.899) and positively correlated with the PCV (P=0.008; rs=0.779). No other significant correlations with laboratory parameters were found. Similarly, the clinical score was not correlated with PON-1 activity.

PON-1 has an established role in modulating oxidative stress, which is a major promoter and mediator of the systemic inflammatory response occurring in sepsis (17). The activity of PON-1 during septic inflammation has been evaluated in other species (18,20,25,29,30), but not in horses yet. We investigated plasma PON-1 activity following intravenous injection of 30 ng/kg of LPS (E. coli O55:B5) in healthy horses included in a previous study (31). The authors of the previous study demonstrated significant clinical changes caused by endotoxemia within the first 12 hours post-infusion, significant changes in WBC counts 6 hours and marked neutrophilia at 24 hours after LPS infusion. Then, all these changes normalized in all horses after 48 hours. Plasma iron concentration significantly decreased to lowest values at 12 hours post-infusion and raised again starting from 24 hours, returning to baseline values at 36 hours. As expected, we observed a decrease in PON-1 activity. Differently from clinical signs and changes in WBC and plasma iron reported in the previous study (31), PON-1 activity recorded in the present study did not show significant changes in the first 12 hours. On the contrary, a significant decrease in PON-1 activity was recorded starting from 48 hours post-infusion, when all the other clinical and analytical parameters had returned to normal reference intervals. The simultaneous decrease in PON-1 activity and recovery from clinical signs is in contrast with those studies that in humans reported PON-1 increase when patients with naturally occurred sepsis clinically improved (18,19,22). The same studies however (19,22), reported a sustained decrease in PON-1 activity for several days, which we also observed. Our study is based on an experimental model of endotoxemia, which does not completely mimic the conditions and pathologic pathways of naturally occurring endotoxemia. In the previous study (31) the evaluation of short-term effects of LPS infusion (i.e. 0-6 hours after LPS administration) was based on clinical changes and not on a complete SIRS score, that also includes the evaluation of WBC count. However, all the horses had at least 2 alterations of clinical parameters consistent with SIRS status evaluation proposed by Roy et al. (32) and therefore it can be assumed that LPS administration induced a systemic inflammatory reaction. Our results agree with other papers assessing PON-1 activity in experimentally induced endotoxemic animals. In dogs, Tvarijonaviciute et al. (20) reported normalisation of clinical signs in 48 hours after LPS administration (although clinical signs occurred earlier compared with horses included in our study), and decreased PON-1 activity at 30 hours, which progressed and became significant at 48 hours compared to 24 hours; a similar trend to what we observed. These authors did not measure PON-1 activity over 48 hours post LPS administration, so a comparison of long-term normalisation of PON-1 activity cannot be made. Feingold et al. (27) found in Syrian hamsters a progressive decrease in PON-1 activity, already significant 8 hours after LPS administration, which even in this case persisted at least up to the last sampling at 48 hours. These and our results seem to state that experimentally induced endotoxemia induces changes in PON-1 activity that does not have a rapid resolution, contrarily to clinical signs, that normalize earlier. This latter discrepancy may explain the lack of significant correlations between PON-1 activity and the clinical score. Our data seem to state that endotoxemia triggers changes in PON-1 activity later and for a longer period, compared with leukocyte count and plasma iron concentration. Again, this delayed response may explain the lack of correlations between PON-1 activity and many laboratory changes, except for fibrinogen that, being a positive acute phase protein, negatively correlated, as expected, with PON-1 activity and for the PCV that increased soon after LPS infusion likely due to dehydration and then decreased to normal values, thus paralleling the late decrease of PON-1. This late PON-1 response could be interpreted as a delayed occurrence of inflammatory oxidations and oxidative stress, possibly due to a different PON-1 metabolism during inflammation in horses compared to other species, as suggested by Ruggerone et al. (15). Otherwise, it may also be possible that anti-inflammatory oxidations occurred in the first 12 hours post-LPS infusion, determining PON-1 activity fluctuations not wide enough to produce significant changes, possibly because of a less severe oxidative stress in horses compared to other species (Ruggerone et al., 2020). A reduced hepatic synthesis, due to cytokine down regulation or to liver function impairment after LPS administration, could have determined the subsequent noticeable decrease of PON-1 activity from the third day up to the seventh. Feingold et al. (27) simultaneously evaluated also liver PON-1 mRNA expression and observed an earlier and greater decrease in mRNA level, starting from 4 hours post-LPS administration and reaching lowest values at 16 hours, followed by a progressive increase which did not reach baseline values at 48 hours. This led to the hypothesis that acute changes in PON-1 production mildly affect serum levels, possibly because of a relatively long half-life of the enzyme (27). Liver expression of PON-1 mRNA was not evaluated in our study, but a similar mechanism would explain the delayed and sustained decrease in PON-1 activity that followed clinical recovery and normalisation of other laboratory parameters. Investigation of PON1 liver expression in the future may clarify the causes of delayed and prolonged decrease of PON-1. Furthermore, PON-1 activity is dependent on the lipid and protein composition of HDL (33), and correlation with lipid profile and other markers of inflammation such as serum amyloid A, may help acquiring knowledge about PON-1 metabolism in this species.

Biomarkers of sepsis so far evaluated in horses include interleukin-1β (IL-1β), interleukin-10 (IL-10), interleukin-6 (IL-6), serum amyloid A (SAA), soluble CD14 (sCD14) and procalcitonin (34,35). Measurement of sCD14 provided contrasting results: no significant differences in concentration were recorded among time in experimental settings (34), while sCD14 was higher in in spontaneous clinically endotoxemic than nonendotoxemic horses, showing however no correlation with LPS concentration (36). In many studies involving different types of experimentally induced endotoxemia in horses, cytokine expression was rapidly upregulated. Following LPS infusion, IL-1β and IL-6 gene expression peaked at 60 and 90 minutes respectively and decreased to still significantly higher levels than baseline 3 hours post infusion (37). In a similar way, serum TNF-α increases within 30 minutes, peaks at 60 minutes, and decreases 2-3 hours from endotoxin administration (37,38). Even if studies about SAA in experimentally induced endotoxemic horses are not available, blood SAA concentration is reported to increase up to 1000 times 6 hours after inflammatory stimuli and decrease within 12 hours after stimulus removal (39–41). It is not known if infection causes an earlier or persistent increase in SAA concentration compared with non-infectious inflammation, but there is evidence that infections are particularly effective in producing strong SAA responses (42), especially in neonatal sepsis (43). Since SAA is produced by the liver in response to cytokines stimulation, it is reasonable to think its increase in circulation be delayed. A decrease in PON-1 activity would be expected together with the early increase in SAA levels, since during the acute phase response the latter displaces PON-1 in HDL (44) and these two acute phase proteins were reported to be inversely correlated (45). However, cytokine-dependent hepatic regulation could have major impact on PON-1 activity rather than displacement by SAA (46), and this would explain the delayed decrease of PON-1 activity, as reported above. Comparing changes in PON-1 activity detected in this study and changes in other markers investigated in experimentally-induced endotoxemic horses, it seems that other markers normalise before PON-1 decreases. In fact, CCL-2 and IL-10 concentrations increased, peaked and decreased within 24 hours post-infusion. Procalcitonin as well showed a similar trend, but its concentration, even if decreased, was still statistically higher than baseline 24 hours post-infusion (34). However, endotoxin is a single factor implicated in the development of sepsis, and it is well known that differences exist between experimentally-induced and clinical endotoxemia and sepsis (47). In humans, PON-1 activity and CCL-2 concentration have an inverse correlation during natural infection (48) and CCL-2 decreases together with the increase of PON-1 and the resolution of naturally occurring septic processes after several days of hospitalisation (19). Investigation and comparison of changes in these markers during natural infection in horses would clarify their behaviour, relationship and usefulness in this species. This study has some limitations. Firstly, the long storage of samples that may have in part affected the magnitude of PON-1 activity. A previous study demonstrated that 6 months storage at -20°C can artifactually slightly increase PON-1 activity in dogs (49). However, no information on storage stability at -80°C, or storage studies on equine PON-1 are available. However, as a support of the hypothesis of a storage effect, PON-1 activity was lower than the reference intervals (28) in most of the horses at T0 despite the lack of any clinical or laboratory abnormality associated with inflammation. Nevertheless, this effect, if any, was present for all the samples included in this study and despite possible storage artifacts, fluctuations of PON-1 activity consistent with endotoxin-induced inflammation were present. A second limitation is the low caseload, coupled with the lack of a control group inoculated with a sham solution: this approach, that however, is in line with other studies based on a complex study design and is supported also by ethical reasons. However, also in this case, such a low but well standardized caseload, on which post-inoculation results were compared with baseline values recorded before LPS administration, allowed to have a better overview of the possible effect of LPS infusion on PON-1 activity compared with in field studies, on which several variables cannot allow to evaluate the direct effect of sepsis on clinical and laboratory parameters. Undoubtedly, following an inflammatory stimulus of septic type, such as the administration of endotoxins, PON-1 activity decreases, as reported for other species. According to our results, plasma iron concentration appears to be an earlier marker of sepsis onset and positive resolution compared to PON-1 activity. However, all horses showed a normalisation of PON-1 activity to baseline values 10 days after LPS administration. As claimed by Oliveira-Filho et al. (31), the inflammatory model adopted by the authors is safe and efficient and caused an acute systemic inflammation without prolonged inflammatory effects. As noted above, in naturally occurring sepsis, clinical and pathological conditions are not as well standardised. Therefore, in natural situations, where the extent and severity of inflammation (17) are very variable, PON-1 might prove to be useful as a diagnostic or prognostic marker of sepsis. In this case, measurement of PON-1 activity could be useful where limitations of iron measurement in detecting systemic inflammation exist, for example during corticosteroid administration, iron supplementation, haemolysis and age-relate variability (50).

This is the first study reporting PON-1 activity in horses with ongoing endotoxemia caused by experimental LPS administration. As expected, LPS infusion induced a progressive transient decrease of PON-1 activity, which became maximum from 3 days to 7 days post-infusion, followed by a normalisation to pre-infusion levels the tenth day. The inflammation model employed in the study does not mimic the variety and severity of septic diseases occurring in the clinical practice. Therefore, further studies are warranted to investigate changes in PON-1 activity during natural onset of endotoxemia in horses. However, our data suggest that measurement and monitoring of PON-1 activity might be useful to evaluate progression of the septic process and recovery in endotoxemic horses and possibly to diagnose it.

The study was performed on 66 plasma samples from six non-pregnant 6-9 years old clinically healthy Quarter Horse mares, with mean body weight 425 (± 20) kg, previously sampled during another study (31). The horses belonged to the São Paulo State University (Unesp), School of Veterinary Medicine and Animal Science, herd. All experiments were carried out according to the São Paulo State University (Unesp), Institutional Animal Care and Use Committee (108-A/2007).

In these animals, endotoxemia was induced by intravenous infusion of 30 ng/kg of LPS (E. coli O55:B5, Sigma-Aldrich, St. Louis, MO, USA) in 300 ml of 0.9% sterile NaCl over 30 min, with blood samples collected at time 0 hours (immediately before LPS infusion) and at several time intervals from 2 to 240 hours after infusion. Blood samples were collected through a 14G catheter aseptically inserted in the right jugular vein. Heparinized samples were used to perform a cell blood count (only at some time point) and then centrifuged. Aliquots of plasma were used to measure total protein, serum iron and fibrinogen, and then stored at -80°C until the analysis. Part of the aliquots were transferred on dry ice to the University of Milan for the measurement of PON-1. Details of the haematological and biochemical parameters that were investigated in the previous study (31), as well as the clinical score and laboratory results recorded at the different time points selected for the current study are reported as supplementary material. To summarize, all horses subjected to LPS infusion showed clinical signs related to endotoxemia, such as depression, muscle fasciculations, intestinal hypomotility and mild-to-moderate abdominal pain and they had a significant increase in the clinical score proposed by Moore et al. (51) based on heart and respiratory rate and of body temperature from 1 to 6 hours (P<0.01). Starting from 12 hours and up to 240 hours post-infusion, clinical score was reported as normal. Conversely, neutrophilic leucocytosis, lymphopenia and decreased plasma iron were detectable between 6 and 24 hours, then gradually normalized over time, with the return to normal levels at 72 hours (31). All animals showed no sequelae at the end of the study and returned to the activities they performed before the study.

On the basis of clinical score and laboratory data, the current study was done on samples collected at time 0, 2, 6, 12, 24, 36, 48, 72, 168, and 240 hours after infusion, to concentrate the analysis in samples that had the most prominent clinical or laboratory changes and to include two additional samples (168 and 240 hours) to assess possible long term effects on PON-1 activity.

Plasma PON-1 activity was measured spectrophotometrically using an automated analyser (Cobas Mira, Roche diagnostic, Basel, Switzerland), and the enzymatic method already validated in horses (28). Briefly, 6 µL of samples were incubated at 37°C with 89 µL of distilled water and 100 µl of reaction buffer (glycine buffer 0.05 mM, pH 10.5 containing 1 mM of paraoxon-ethyl, purity > 90% [Sigma-Aldrich, Saint Louis, MO, USA], and 1 mM of CaCl₂). The rate of hydrolysis of paraoxon to p-nitrophenol was measured by monitoring the increase in absorbance at 504 nm using a molar extinction coefficient of 18.050 L· mol^-1 · cm^-1 as previously suggested (27). The unit of PON-1 activity expressed as U/mL is defined as 1 nmol of p-nitrophenol formed per minute under the assay conditions.

Statistics were run with Analyse-it v 5.01 (Analyse-it Software Ltd, Leeds, United Kingdom) statistical analysis add-in software for Excel (Redmond, WA, USA). Since the Shapiro-Wilk test demonstrated that data were not normally distributed, data recorded in the different sampling times were compared to each other using a non-parametric ANOVA test for repeated measurements (Friedmann test) followed by the Wilcoxon signed rank test to compare paired results recorded at each sampling time. The Spearman test was used to investigate the possible correlation between mean PON-1 activity and mean values of the clinical or laboratory changes recorded in the previous study (31). Statistical differences were set for P<0.05.

HDL: high-density lipoproteins

LPS: Lipopolysaccharide

PON-1: Paraoxonase-1

SIRS: systemic inflammatory response syndrome

Ethics approval and consent to participate: All experiments were carried out according to the São Paulo State University, Institutional Animal Care and Use Committee (108-A/2007).

Consent for publication: Not applicable.

Availability of data and materials: Raw data are available upon request.

Competing interests: The authors declare that they have no competing interests

Funding: The authors did not receive financial support for the research, authorship, and/or publication of this article.

Authors' contributions: ASB and JPOF designed the animal phase of the study. SP, DS, VV and MS designed the laboratory part of the study and analysed the results. SP and DS measured PON-1 activity and drafted the manuscript. All authors reviewed and approved the final manuscript.

Acknowledgements: Not applicable.

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BVETD2000738R1additionalfile.pdf
Additional file 1: mean ± standard deviation regarding the clinical score and the main clinoco-pathological changes recorded in the previous study (31) in the time points selected for inclusion in this study

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Serial measurements of Paraoxonase-1 (PON-1) activity in horses with experimentally induced endotoxemia

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