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. 2006 May 17;2006(4):60285. doi: 10.1155/MI/2006/60285

Hyperglycemia in Streptozotocin-Induced Diabetes Leads to Persistent Inflammation and Tissue Damage Following Uveitis Due to Reduced Levels of Ciliary Body Heme Oxygenase-1

Settimio Rossi 1, Michele D'Amico 1,*, Annalisa Capuano 1, Mary Romano 1, Pasquale Petronella 1, Clara Di Filippo 1
PMCID: PMC1618950  PMID: 17047293

Abstract

This study investigated the heme oxygenase-1 (HO-1) and the endotoxin-induced uveitis (EIU) in diabetic streptozotocin (STZ)-hyperglycemic rats. STZ-hyperglycemic rats had impaired levels of the enzyme HO-1 within the ciliary bodies if compared with the nondiabetic rats. STZ-hyperglycemic rats also predisposed the eye to produce high levels of both the cytokines IL-1β and CXCL8. Subsequent EIU further and significantly (P < .01) increased the cytokines production, an effect partly prevented by hemin treatment. Most importantly, hemin, an inducer of heme oxygenase expression and activity, recovered the huge number of infiltrated polymorphonuclear leukocytes PMN within the ciliary bodies associated with STZ-hyperglycemic state and EIU damage. Impairment of the stress-sensitive enzyme HO-1 in STZ-hyperglycemic rats increases and prolongs the inflammatory response to EIU.

INTRODUCTION

Endotoxin-induced uveitis (EIU) is an animal model of acute ocular inflammation. Cytokines, chemokines, and nitric oxide (NO) have been reported to play important roles in promoting the inflammation and cell injury of the ciliary bodies in this pathology. Usually, this experimental pathology lasts up to 72 hours and has similarities with the human pathology [1].

Interestingly enough, the cell damage induced by the EIU is strongly reduced by the heme oxygenase (HO)-1 [2]. HO-1 in injured tissues represents an adaptive and defensive response to the inflammatory process [3], and during EIU it has protective effects against the ocular inflammation induced by lipopolysaccharide (LPS) by down-regulating proinflammatory cytokines expression in normoglycemic rats [2].

Several studies have demonstrated that diabetes is a risk factor for developing ocular diseases, increasing their prevalence and severity. Progression to severe eye pathologies with loss of supporting structures is mediated by several factors, including oxidative stress, free radicals, secretion of a broad spectrum of inflammatory, and destructive mediators such as cytokines (TNF-alpha, IL-1b, and IL-6), chemokines (IL-8), and prostaglandin E2. This is caused by indirect effects of hyperglycemia [4].

The present study focuses on the likelihood that hyperglycemia in diabetes worsens the inflammatory response of EIU by interfering with the HO-1 expression and activity. We used LPS for the induction of EIU and streptozotocin to induce diabetes, insulin 1.5 ± 0.5 U/day for 8 days to yield hyperglycemia (blood glucose levels of approximately 22 mmol/L; 396 mg/dl) (poor glycemic controlled rats).

MATERIALS AND METHODS

All experimental procedures and protocols used in this investigation were reviewed and approved by the Animal Care and Use Committee of the Medical College of Naples. Experiments were conducted in male Sprague-Dawley rats (four to six months old and weighing on average 250 g), diabetes was induced according to the described procedures [5]. Particularly, streptozotocin was administered at 70 mg/kg ip and insulin (1.5 ± 0.5 U/day ip) was applied to rats in order to yield blood glucose levels of approximately 22 mmol/L (396 mg/dl) for 8 days (poor glycemic controlled rats).

Induction of EIU

Rats were injected in one footpad with 200 μg of lipopolysaccharide (LPS, Salmonella minnesota, Sigma, St Louis, Mo, USA) in 0.1 mL of sterile pyrogen-free saline [6].

Treatment with hemin

An intraperitoneal injection of 50 mg kg−1 hemin (Fluka, Buchs SG, Switzerland), an inducer of HO-1, was given 1 hour before LPS injection. The dose of hemin (50 mg kg−1) was chosen in accordance with previous studies in rats [2, 7, 8]. In addition zinc protoporphirin-IX (ZnPP-IX) was used as inhibitor of the HO-1 at dose of 50 μg/kg ip.

Experimental groups

Rats were randomly allocated to the groups shown in Table 1. Nondiabetic and diabetic animals were sacrificed at 0, 6 h, 12 h, 18 h, 24 h, 48 h, 72 h (n = 6 for each time point) when treated with vehicle alone and at the same time points when added of LPS in all other groups.

Table 1.

Schematic representation of the experimental groups and measures done for each group.

Experimental groups Measures
Nondiabetic rats Diabetic rats (streptozotocin, 70 mg/kg ip) In each group the levels of the following parameters were measured: HO-1, MPO, IL-1beta, CXCL8
Vehicle (saline, 0.1 mL) Vehicle (saline, 0.1 mL)
Vehicle + LPS (200 μg in 0.1 mL) Vehicle + LPS (200 μg in 0.1 mL)
Hemin (50 mg/Kg ip in 0.1 mL, 1 h prior to LPS) Hemin (50 mg/Kg ip in 0.1 mL, 1 h prior to LPS)
Zn-PP (50 μg/Kg ip, 6 h before hemin)+LPS Zn-PP (50 μg/Kg ip in 0.1 mL, 6 h before hemin)+LPS
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The iris-ciliary body samples

The iris-ciliary body (ICB) samples were dissected from the eyes, collected, homogenized, and centrifuged to remove cellular debris. Subsequently the frozen ciliary body tissues were homogenized in a solution containg 0.5% hexa-decyl-trimethyl-ammonium bromide dissolved in 10 mM potassium posphate buffer (pH 7) and centrifuged for 30 min at 4, 000 xg at 4°C.

HO-1 quantitation

This assay was done by using an ELISA kit supplied by Stressgen Biotech Corp (Victoria, BC, Canada). This kit shows sensitivity of 0.78 ng/mL and ranges up to 25 ng/mL as furnished by Stressgen. An aliquot (100 μl) of tissue supernatant was used.

Myeloperoxidase activity

The reaction was performed as previously described [9]. Data are reported as units of Myeloperoxidase (MPO) activity per gram of tissue protein (U/g). A standard curve was constructed with different numbers of rats neutrophils that were elicited into the peritoneal cavity at 4 h in response to application of 5 mL thioglycollate. Pellets were subjected to three cycles of freeze-thawing. Samples (100 μl) were obtained after a final centrifugation at 13,000 rpm for 30 min on a benchfuge. The MPO reaction was produced with a PMN number ranging from 0 to 220 × 103, obtaining a linear relationship with the absorbance at 620 nm following the equation: A620 = 4.488× no. of PMN +33.74, with a R2 = 0.98083. Data are reported as equivalent numbers of PMN per mg of tissue.

Cytokine quantitation by ELISA

Tissue IL-1β levels in tissue homogenates (50 μl) were determined using a commercially available ELISA specific for the rats cytokine, purchased from R&D Systems (Abingdon, UK). Briefly, tissue supernatant aliquots (50 μl) were assayed for IL-1β and compared to a standard curve constructed with 0-1 ng/mL of the standard cytokine. The ELISA showed negligible (<1%) cross-reactivity with several murine cytokines and chemokines (data as furnished by manufacturer). A similar procedure was followed for determination of the chemokine CXCL8 by ELISA (R&D Systems, UK) and used according to the manufacturer instructions.

Drugs

STZ, ZnPP-IX were purchased from Sigma-Aldrich (Milan, Italy); this latter compound was dissolved in saline (vehicle).

Statistical analysis

All values are expressed as mean ± SEM of number (n) of rats for the in vivo experiments. Statistical analysis was assessed either by Student's t test (when only two groups were compared) or one-way ANOVA followed by Dunnett's test (more than two experimental groups). A probability P value less than 0.05 was considered significant to reject the null hypothesis.

RESULTS

STZ-hyperglycemic rats

Blood glucose averaged 6.2 ± 0.1 mmol/l in basal conditions and rose to 23.0 ± 2 mmol/L 15 hours after STZ administration. In STZ-rats, a repeated intraperitoneal intravenous infusion of regular insulin (1.5 ± 0.5 U/day) was given and adjusted to yield blood glucose levels of approximately 22 mmol/L (396 mg/dl) for 8 days. Serum sodium and potassium concentrations and body weight did not significantly change after STZ-treatment (data not shown).

HO-1 quantitation

In vehicle treated nondiabetic rats ciliary bodies HO-1 level was not appreciable as evidenced by HO-1 ELISA over the time (Figure 1). HO-1 level significantly (P < .05) increased after EIU in nondiabetic rats treated with LPS starting 12 h post-LPS, reaching a value of 788 ± 42% respect to baseline 12 h later (P < .001). Administration of hemin prior to EIU produced a further and significant increase of HO-1 at all the times (Figure 1). ZnPP-IX+hemin prior to LPS strongly restored the values of HO-1 detected following the LPS alone (data not shown).

Figure 1.

Figure 1

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STZ-diabetes and HO-1 levels following EIU. Rats were treated ip with vehicle saline; LPS alone (nondiabetic); LPS+STZ (diabetic), or hemin (50 mg/kg 1 h prior to LPS or LPS+STZ). Significance is expressed as •P < .05 versus vehicle saline nondiabetic rats; * P < .05 and ** P < .01 versus LPS nondiabetic rats; ° P < .05 and °° P < .01 versus LPS+hemin nondiabetic rats.

HO-1 was already present in ICB after 8 days of poor glycemic control (Time 0 saline, +83.3 ± 11% versus time 0 nondiabetic; see Figure 1). This HO-1 level remained almost steady even 24 h later (data not shown). Interestingly, the treatment with LPS increased the levels of HO-1 starting 6 h after the injection with a peak value at 24 h time point. This increase was 68 ± 4% lower than the incremental expression seen in nondiabetic rats at same 24 h time (P < .001). LPS-induced HO-1 expression felt within the following 24 and 48 hours (Figure 1). Although hemin treatment, the inducer of HO-1, increased (P < .01) all the figures seen in STZ-diabetic rats (Figure 1), the maximum increases in these rats were lower than those observed in LPS-induced nondiabetic rats subjected to the same treatment and compared at similar time points. This effect on the HO-1 levels started 18 h after LPS and lasted 72 h (Figure 1). ZnPP+hemin did not modify the levels observed in the LPS-diabetic condition alone (data not shown). Therefore hyperglycaemia impairs the levels of HO-1 within the ciliary body, a situation patially restored by hemin.

PMN associated EIU damage

In nondiabetic rats EIU was paralleled by increase in MPO activity in the ciliary bodies versus control rats (ie, saline, time 24 h, 93 ± 14 equivalent PMN number/mg tissue; LPS time 24 h, 640 ± 30 equivalent PMN number/mg tissue, P < .001). This LPS-induced MPO value decreased within the following 24 and 48 hours (Figure 2). Administration of hemin produced an attenuation in MPO activity as measured 24 h post-LPS and at other time points (Figure 2). This attenuation in MPO activity was absent in the rats treated with the hemin + ZnPP (data not shown).

Figure 2.

Figure 2

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Myeloperoxidase activity (MPO) in ciliary body. Rats treated as described in Figure 1 had ciliary body collected at the end of the 24 h endotoxin-induced uveitis and MPO activity determined. Values are mean ± SEM of n = 6 rats per group. Significance is expressed as •P < .05 versus vehicle saline nondiabetic rats; *P < .05 and **P < .01 versus LPS nondiabetic rats; °P < .05 and °°P < .01 versus LPS+hemin nondiabetic rats.

Control STZ-hyperglycemic rats showed increase in MPO activity with respect to nondiabetic control rats administered with same saline (saline STZ-rats, 152 ± 28 equivalent PMN number/mg tissue; saline nondiabetic, 93 ± 14 equivalent PMN number/mg tissue, P < .05). LPS procedure further increased the values of MPO up to 24 h while decreasing later (Figure 2). The MPO values in STZ-rats were still higher than those in normoglycemic rats (Figure 2) compared at same points. Administration of LPS + hemin produced MPO levels still higher than the nondiabetic values measured at any time considered post-LPS (Figure 2). However the association with ZnPP-IX reduced the MPO values almost at same values of STZ-EIU rats (data not shown). Hyperglycaemic diabetes produces a worsening of the MPO activity within ICB following uveitis. By potentiating the HO-1 pathway with hemin this MPO activity is almost restored to values of the nondiabetic condition.

Cytokine levels in the ciliary bodies

At 24 h time point ciliary bodies IL-1β and CXCL8 levels were slight appreciable in control nondiabetic rats, (saline, 22 ± 3 pg/mg tissue and 100 ± 26 pg/mg tissue, resp). LPS-induced uveitis showed 24 h levels of the IL-1β and CXCL8 up to values of 210 ± 21 pg/mg tissue and 590 ± 34 pg/mg, respectively. The important issue is that the tissue levels of these cytokines after 48 h and 72 h were decreased (Figure 3). Hemin prior to the LPS produced a significant reduction in IL-1β and CXCL8 levels within the tissue (Figure 3). This reduction was absent in the rats treated with the hemin+ZnPP-IX (data not shown).

Figure 3.

Figure 3

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HO-1 induction reduces cytokine levels in the ciliary body. Tissues at each time point of the EIU procedure were collected from n = 6 rats for each group and were analysed for IL-1β or CXCL8 determined by ELISA. Significance is expressed as •P < .05 versus vehicle saline nondiabetic rats; *P < .05 and **P < .01 versus. LPS nondiabetic rats; °P < .05 and °°P < .01 versus LPS+hemin nondiabetic rats.

STZ-hyperglycemia predisposed the eye to produce high levels of both the cytokines IL-1β and CXCL8 as assayed 24 h after saline injection (ie, 83 ± 14 pg/mg tissue and 198 ± 30 pg/mg tissue, resp). Subsequent EIU further and significantly (P < .01) increased the cytokines production (Figure 3). Hemin decreased the cytokines production with levels being still higher than those in nondiabetic rats (Figure 3). The association of ZnPP-IX and hemin report the cytokine levels to almost the values assayed in the rats subjected to STZ treatment (data not shown).

Ciliary IL-1β and CXCL8 increase after EIU in nondiabetic LPS-rats and much more following the concomitance of diabetes. The inducer of the HO-1 activity hemin protects the eye from the release of cytokines both in normoglycaemic and hyperglycaemic states. However the effect of this compound in this latter circumstance is lower, in agreement with results shown on the fact that the endogenous HO-1 is impaired by the diabetes.

DISCUSSION

This study shows that 8 days of hyperglycemia or poor glycemic control in STZ-diabetic rats lead to more persistent inflammation and tissue damage following EIU. The inflammatory response was evidenced here by higher and more prolonged production of cytokines and chemokines as well as PMN infiltration into the ciliary bodies of STZ-hyperglycemic rats compared with nondiabetic rats. In spite of several reports in humans and animals addressing (i) the stimulation of an inflammatory response and release of inflammatory mediators by diabetes [10] and (ii) the importance that this response has on the severity of different pathologies [11] the present study is noteworthy the first report showing that this condition also enhances the inflammatory response during the EIU.

This study also shows the likelihood that STZ-hypergly-cemia causes increased and prolonged inflammation during EIU by impairing the expression of the enzyme HO-1 within the ciliary tissues. HO-1 in injured tissues represents an adaptive and defensive response to the inflammatory process [3], and during EIU it has protective effects against the ocular inflammation induced by lipopolysaccharide by down-regulating proinflammatory cytokines expression in normoglycemic rats [2]. Both LPS-induced ocular response and the expression of the HO-1 enzyme seem to appear earlier in the STZ-hyperglycemic rats than in normoglycemic ones. They are already and significantly present in rat ciliary bodies in basal conditions, 6 hours after LPS, increased 18 hours later by reaching the maximum level, and felt within the following 24 and 48 hours. So, diabetes by inducing per se oxidative stress anticipates the insurgence of LPS-induced events, both inflammatory and HO-1 response. Noteworthy, pathophysiological stimuli that increase oxidative stress upregulate HO-1 [12, 13]. In addition to the facts expressed not so far, the evidence that there is difference between the levels of HO-1 found at the peak of the inflammatory response in nondiabetic rats and those in STZ-rats, both subjected to EIU, argues the interesting hypothesis that inflammatory episodes, that increase HO-1 in nondiabetic rats, when superimposed on preexisting hyperglycemia-mediated stress would result in the impairment of the burst of HO-1 expression. This contention based on the fact that the HO-1 levels in STZ-EIU-rats may have been impaired by the high production of reactive oxygen species and reduced NO availability occurring in diabetes [5, 14]. The high peroxinitrite levels formed into the eye may have reduced the NO, thus impairing the HO-1 expression. Actually, NO derived from iNOS enhances HO-1 expression in the tissues [15].

Ciliary bodies of STZ-rats showed higher levels of MPO activity, a marker used to monitor tissue infiltration by PMN [9], even 48 h and 72 h after LPS, with respect to nondiabetic normoglycemic rats subjeted to EIU, in contrast to the low levels of the protein HO-1 found in the ELISA assay at the same time points. Interestingly, hemin treatment showed less reduction in MPO levels in STZ-rats as compared with nondiabetic rats at any time point considered. This latter observation supported by previous evidence indicating that induction of HO-1 activity results in reduced expression of adhesion molecules, reduced adhesion and migration of leukocytes following an inflammatory stimulus [16, 17].

The causal correlation between HO-1 expression following EIU and white blood cells recruitment into ciliary bodies was confirmed on local generation of leukocyte activators, cytokines, and chemokines which are known to promote leukocyte-endothelium interaction [18]. For this purpose we investigated a cytokine able to increase the adhesive properties of the endothelial wall [19], and that it is implicated in the pathology associated with experimental uveitis [2], the IL-1 beta. As chemokine we chose CXCL8 because it is a chemokine able to recruit neutrophils in rodent species during experimental inflammation [20, 21]. The results of our study showed that the levels of these two cytokines copy the trend observed with the MPO activity. In particular, the reduced HO-1 levels within the ciliary bodies of STZ-hyperglycemic rats subjected to EIU were mirrored by significant increase in both these cytokines with respect to EIU of nondiabetic rats.

In conclusion, our results demonstrated that streptozot-ocin-induced hyperglycemic rats had altered HO-1 levels to counteract LPS-induced ocular inflammation in the ICB. Impairment of this stress-sensitive enzyme increases and prolongs the inflammatory response to EIU. It involves a local increase of the expression of cytokines, increased recruitment of PMN and cell damage. Thus in perspective, pharmacological agents that reduce the oxidative stress in hyperglycemic diabetes may reinforce the HO-1 citoprotection for preventing uveitis as well as in other ocular pathological situations.

ACKNOWLEDGMENT

This work was supported by the Italian MIUR.

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