PPAR Research

Volume 2012 (2012), Article ID 596394, 10 pages

doi:10.1155/2012/596394

Research Article

Expression Pattern of Peroxisome Proliferator-Activated Receptors in Rat Hippocampus following Cerebral Ischemia and Reperfusion Injury

Hong Wang,¹ Rong Jiang,² Qin He,³ Yunmei Zhang,⁴ Yanli Zhang,¹ Yong Li,¹ Ruichun Zhuang,¹ Ying Luo,¹ Yu Li,² Jinyuan Wan,¹ Yong Tang,² Huarong Yu,² Qingsong Jiang,¹ and Junqing Yang1,5

¹The College of Pharmacy, Chongqing Medical University, Chongqing 400010, China

²The College of Basic Medicine, Chongqing Medical University, Chongqing 400010, China

³The First Affiliated Hospital, Chongqing Medical University, Chongqing 400010, China

⁴ School of Nursing, Chongqing Medical University, Chongqing 400010, China

⁵Department of Pharmacology, Chongqing Medical University, Chongqing 400010, China

Received 22 September 2012; Revised 30 October 2012; Accepted 14 November 2012

Academic Editor: Sheng Zhong Duan

Copyright © 2012 Hong Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The present study was designed to investigate the pattern of time-dependent expression of peroxisome proliferator-activated receptors (PPARα, β, and γ) after global cerebral ischemia and reperfusion (I/R) damage in the rat hippocampus. Male Sprague Dawley (SD) rats were subjected to global cerebral I/R. The rat hippocampi were isolated to detect the expression of PPARs mRNA and protein levels at 30 min–30 d after I/R by RT-PCR and Western blot analysis, respectively. The expression levels of PPARs mRNA and protein in the rat hippocampus significantly increased and peaked at 24 h for PPARα and γ (at 48 h for PPARβ) after I/R, then gradually decreased, and finally approached control levels on d 30. The present results suggest that global cerebral I/R can cause obvious increases of hippocampal PPARs mRNA and protein expression within 15 d after I/R. These findings may help to guide the experimental and clinical therapeutic use of PPARs agonists against brain injury.

1. Introduction

Cerebral ischemic injury is the second leading cause of death and a common cause of disability worldwide. Cerebral ischemia can be divided into two groups: global cerebral ischemia and focal cerebral ischemia. The major manifestation of cerebral ischemia is a temporal or permanent reduction in cerebral blood flow, which is insufficient to meet the metabolic or functional demand of the central nervous system (CNS). There was no reperfusion after permanent occlusion of artery. Following transient ischemia or treatment of thrombolysis, reperfusion inevitably occurs. Although the reperfusion is helpful for restoring the supply of blood and oxygen to the CNS, a growing body of evidence supports the viewpoint that reperfusion may exacerbate the injury initially resulting from ischemia and is referred to as cerebral ischemia and reperfusion (I/R) injury. Cerebral I/R can cause serious neuronal injury and death, which can further lead to learning and memory impairment and neurodegeneration.

The pyramidal neurons of the hippocampal CA1 region are essential for spatial learning and memory functions. When suffering from cerebral ischemia insult, the hippocampal pyramidal neurons are the most vulnerable to the reduction of blood supply to the brain, and cell death occurs days after the initial ischemic insult, a phenomenon termed “delayed neuronal death” [1]. Currently, the mechanisms of neuronal injury and death induced by cerebral I/R are not completely known, and therefore an effective therapy for ischemic cerebral damage has remained elusive. Recently, much evidence has emerged indicating that the peroxisome proliferator-activated receptors (PPARs) are promising candidates as pharmacological targets for cerebral ischemic damage [2, 3].

PPARs, which are ligand-activated transcription factors belonging to the nuclear receptor superfamily, have three isoforms, α, β/δ, and γ. Depending on differences in their tissue distribution and transcription of target genes, the three PPAR subtypes show distinct physiological and pharmacological functions. PPARs are expressed in neurons of numerous brain regions, especially in the hippocampus [4–6]. It is well known that CNS inflammation and oxidative stress are involved in pathophysiological mechanisms of cerebral damage. In addition to regulating metabolism, activation of PPARs results in anti-inflammatory and antioxidative effects by transrepression of transcription factors (e.g., NFκB) [7]. Recent studies have shown that activation of PPARs is helpful in regulating neuronal death in ischemic brain injury and neurodegenerative diseases.

Prophylactic administration of gemfibrozil, a PPARα selective agonist, was shown to significantly reduce the infarct area and improve cortical blood flow in mice with permanent middle cerebral artery occlusion [8]. Collino et al. also reported that the PPARα agonist WY14643 can significantly depress cerebral oxidative stress and inflammatory responses induced by transient cerebral ischemia reperfusion and that the effect of WY14643 can be abolished by the administration of MK886 (an antagonist of PPARα) [9].

PPARβ-null mice exhibit a significant increase in the infarct size in a model of focal cerebral ischemia by middle cerebral artery occlusion (MCAO) [10, 11]. Intracerebroventricular administration of PPARβ agonist L-165041 or GW501516 can significantly attenuate the ischemic brain infarct size 24 h after a transient middle cerebral artery occlusion/reperfusion [12]. Another PPARβ agonist, GW0742, has also demonstrated an obvious protective effect against cerebral damage induced by global cerebral I/R in rats [13]. Pereira, et al. found that L-796449, a synthetic nonthiazolidinedione PPARγ agonist, significantly decreases the infarct size induced by permanent MCAO and improves neurological scores and that this protection is related to inhibition of MCAO-induced expression of an inflammatory mediator [14].

Intracerebroventricular administration of pioglitazone, an agonist of the PPARγ, over a 5-day period before and 2 days after MCAO (occlusion of the MCA for 90 min with subsequent reperfusion) was found to reduce the infarct size and the expression of tumor necrosis factor α (TNF-α) and COX-2 [15]. In another study, 129/SV mice were subjected to 30 min filamentous MCAO followed by reperfusion. Pioglitazone given acutely after transient brain ischemia/reperfusion reduced the lesion size. However, analysis at 6 weeks after MCAO/reperfusion indicated that pioglitazone no longer yielded an effect on lesion size [16]. Pioglitazone can also reduce delayed neuronal damage induced by common carotid artery occlusion I/R [17]. Additionally, rosiglitazone (RGZ) (5 mg/kg) intraperitoneally injected at 24 and 48 h after MCA embolization induced by placing a preformed clot into the middle cerebral artery can reduce ischemic injury and improve neurological outcome [18].

These previous studies indicated that activation of the PPAR signaling pathway may have significant protective effects on cerebral damage by I/R, and PPAR agonists may be candidates for ischemic brain injury. This protective effect also depends on the levels of PPAR cofactors [19]. However, the expression of hippocampal PPARs (PPARα, β, and γ) after global and focal cerebral I/R injury has not been characterized.

There are two types of rodent models for clinical cerebral I/R: experimental global ischemia and focal ischemia models. An experimental rat model of global ischemia is established by bilateral common carotid artery occlusions combined with systemic hypotension. This model produces markedly reduced forebrain blood flow and results in a reversible high-grade forebrain ischemia change within selectively vulnerable structures, including the CA1 pyramidal neurons of the hippocampus, caudoputamen, and neocortex. The model is suitable for studying phospholipids and energy metabolism in ischemia and recently has been used for the evaluation of neurotransmitter metabolism, histopathology, spatial learning and memory, and the protective effects of mild cerebral hypothermia and drugs [20]. In order to explore the therapeutic benefits of PPARs agonists for the treatment of ischemic cerebral injury, this study was designed to observe the characteristics of time-dependent expression of PPARs (PPARα, β, and γ) in a rat model of global cerebral I/R.

2. Materials and Methods

2.1. Reagents

The following reagents were obtained commercially: RNAlater RNA stabilization reagent (Qiagen, Germany); BIOZOL total RNA extraction kit (BioFlux, Japan); ReverTra Ace-α reverse transcription kit (TOYOBO, Japan); mouse anti-rat PPARα, β, and γ monoclonal antibodies (1 : 1000) (Abcam, England); mouse anti-rat superoxide dismutase 2 (SOD2) and mitochondrial uncoupling protein 2 (UCP2) monoclonal antibodies (1 : 1000) (Beijing Biosynthesis Biotechnology, LTD, China); BCA (bicinchoninic acid) protein detection kit (Shanghai Biocolors, China); ECL chemiluminescence detection kit (Pierce Biotech., USA); Taq DNA Polymerase (Promega, USA).

2.2. Animals and Experimental Protocol

Male Sprague Dawley rats (, 200–250 g and 8 weeks old) were purchased from the Laboratory Animal Center of Chongqing Medical University, Chongqing, China. They were housed in standard conditions of , % humidity, with 12 h light/dark cycles (light from 8:00–20:00). All experimental procedures were approved by the Chongqing Medical University Institutional Animal Ethics Committee. Rats were divided into one control group receiving a sham operation () or eight experimental groups all receiving global cerebral ischemia followed by reperfusion for 30 min (), 2 h (), 6 h (), 24 h (), 48 h (), 7 d (), 15 d (), or 30 d ().

2.3. Preparation of Rat Global Cerebral I/R Model

Rats were anesthetized with 4% chloral hydrate (1 mL/100 g, ip) and fixed in a supine position. One side of the common vena jugularis and the bilateral common carotid arteries were exposed. Blood (2.4 mL/kg) was taken from the common vena jugularis, and the bilateral carotid arteries were occluded using artery clamps for 20 min. After ischemia for 20 min, the artery clamps were removed followed by blood retransfusion and different periods of reperfusion. Rats in the sham operation group were subjected to the same operation as above, except for the bilateral carotid artery occlusion and hemospasia from the common vena jugularis.

2.4. Morris Water Maze Test

Considering the trauma induced by the operation, only rats in the reperfusion for 7 d after global cerebral ischemia group () were selected to observe changes of learning and memory in a behavior test along with rats in the sham-operated group (). Rat spatial learning and memory were tested using a DMS-2 Morris water maze (Institute of Materia Medica, Chinese Academy of Medical Sciences, Beijing, China) with a diameter of 1.5 meter, height of 0.5 meter, water depth of 0.4 meter, and temperature of 24-25°C. Rats were allowed to learn how to navigate the maze for four days before spatial memory was tested as previously reported [13].

2.5. Pathomorphological Observation

Three rats were selected for histopathological observation at each time point of 30 min, 2 h, 6 h, 24 h, 48 h, 7 d, 15 d, and 30 d after global cerebral ischemia (total of 24 rats). Rats in each group were anesthetized with 4% chloral hydrate (1 mL/100 g, ip) and transcardially perfused with 100 mL of 0.9% saline containing heparin (250 U) followed by 200 mL of fixing solution containing 3.5% formaldehyde and 0.1 M phosphate buffer (pH 7.2). The brain tissue was isolated and cut into coronal sections of 5 μm in thickness. The sections were stained with hematoxylin and eosin (H&E). The histomorphology of neurons in each rat hippocampus was observed by light microscopy. For assessment of cell counts from H&E-stained sections, 10 consecutive high-power fields were sampled from the dorsal hippocampal CA1 subfield. Counts of intact neurons were performed from the ischemic and sham brains using a microscope at 400x magnification, and the extent of cell death was estimated.

2.6. RT-PCR Analysis of PPARs, SOD2, and UCP2 mRNA

Eight sham operation rats and eight rats at each time point of 30 min, 2 h, 6 h, 24 h, 48 h, 7 d, 15 d, and 30 d after global cerebral ischemia were sacrificed (total of 72 rats.) Brains were removed, and the hippocampi were separated for analysis of mRNA and protein expression. Thirty-six of the rat hippocampi were used for expression analysis of PPARs ( per time point) and the other thirty-six for SOD2 and UCP2 ( per time point) by RT-PCR. Total RNA was extracted from the cerebral hippocampus of rats using BIOZOL reagents according to the manufacturer’s directions of the Total RNA Extraction Kit. Sequences of the primers used for RT-PCR amplification and lengths of the products (in brackets) were as follows: PPARα (407 bp) forward 5′-ACGATGCTGTCCTCCTTGATG-3′ and reverse 5′-GCGTCTGACTCGGTCTTCTTG-3′; PPARβ (212 bp) forward 5′-GCCGCCCTACAACGAGATCA-3′ and reverse 5′-CCACCAGCAGTCCGTCTTTGT-3′; PPARγ (143 bp) forward 5′-CCCTTTACCACGGTTGATTTCTC-3′ and reverse 5′-GCAGGCTCTACTTTGATCGCACT-3′; SOD2 (500 bp) forward 5′-GGCACCTTTCTCAGTAGCGG-3′ and reverse 5′-CTAAGGGACCCAGACCCAAC-3′; UCP2 (391 bp) forward 5′-CTACAAGACCATTGCACGA-3′ and reverse 5′-CTCATAGGTGACAAACATTA-3′; β-actin (540 bp) forward 5′-GTGGGGCGCCCCAGGCACCA-3′ and reverse 5′-CTTCCTTAATGTCACGCACGATTTC-3′.

Two-step RT-PCR was carried out according to the system manual. The total reaction volume for RT was 20 μL, including 4 μL 5× RT buffer, 2 μL of 10 mM dNTP, 1 μL of 10 U/μL RNase inhibitor, 1 μL of 10 pmol/μL oligo (dT), 1 μg of RNA template, 1 μL of ReverTra Ace-α, and 10 μL of RNase-free H₂O. The RT conditions were 30°C for 10 min, 42°C for 20 min, 99°C for 5 min, and 4°C for 5 min. The total reaction volume for PCR was 25 μL, including 5.0 μL of cDNA, 0.5 μL of 10 mM dNTP mixture, 2.0 μL of 25 mM MgCl₂, 2.5 μL of 10× PCR buffer, 0.5 μL of forward/reverse primers, 0.125 μL of 2.5 U/μL Taq DNA Polymerase, and 13.875 μL of sterile double-distilled water. The PCR conditions were 94.0°C for 4 min, 35 cycles of 94.0°C for 15 s, 55.2°C for PPARα (57.0°C for PPARβ, 53.1°C for PPARγ, and 55°C for SOD2 and UCP2) for 15 s, and 72.0°C for 40 s, followed by extension at 72.0°C for 5 min.

The PCR products were visualized after electrophoresis on a 1% low melt point agarose gel and stained with 0.5 μg/mL ethidium bromide for 10 min. The integrated gray values of the product bands were measured using a gel imaging and analysis system (Bio-Rad, Hercules, CA, USA). The PPAR, SOD2, and UCP2 mRNA levels were calculated as ratios of the corresponding β-actin mRNA level (PPARs, SOD2, and UCP2/β-actin).

2.7. Western Blot Analysis of PPARs Protein Expression

Proteins from the hippocampal tissues were extracted by adding 0.5 mL of tissue lysate solution and then by centrifuging at 12,000 ×g for 5 min at 4°C. The supernatant was collected for Western blotting analysis. The protein concentration was detected by the BCA method according to the manufacturer’s directions of the protein detection kit. The proteins (50 μg per sample) were separated by 10% (weight/volume) sodium dodecyl sulfate polyacrylamide gel electropheresis (SDS-PAGE) and then transferred to a polyvinylidene difluoride (PVDF) membrane. The membrane was blocked for 1.0 h in PBS containing 5% fat-free milk (weight/volume) and 0.2% Tween 20 (vol/vol). The blot was incubated overnight at 4°C with antibodies either to PPARs, SOD2, UCP2, or β-actin at 1 : 1000 dilution, followed by incubation for 1 h at 37°C with a secondary antibody (1 : 1000). Immunoreactive bands of PPARs, SOD2, UCP2, and β-actin were visualized with an ECL chemiluminescence detection kit, and the optical density bands were detected using a gel imaging and analysis system (Bio-Rad). The protein levels of PPARs, SOD2, and UCP2 were calculated as ratios of the corresponding β-actin protein level.

2.8. Statistical Analysis

All data were calculated as mean ± SD. The differences between groups were evaluated using one-way analysis of variance (ANOVA), followed by Dunnett’s t-test analysis to compare between the I/R-treated group and sham operation group with the SPSS12.0 software package. Results were considered statistical significantly with values <0.05.

3. Results

3.1. Morphological Changes of Rat Hippocampus

Rat hippocampal neurons in the sham operation group were closely arranged and well structured, with clear and intact cellular form and structure. Meanwhile, neuronal karyopyknosis and reduction in the number of neurons were observed in the hippocampal CA1 subfield in I/R rats (Figures 1(a) and 1(b)).

(a)

(b)

Figure 1: Morphological change of rat hippocampal neurons induced by I/R. (a) Representative pictures of H&E stained CA1 section, 400x. Scale bars = 50 μm. (b) Group data showing the cell death rate. compared with vehicle sham group ().

3.2. Changes in Spatial Learning and Memory in Rats

Compared with that in the sham operation group, the time for rats to learn to navigate the maze from d 2 to d 4 significantly increased in the 7 d reperfusion group. For spatial memory function in rats, the time taken to find the platform was significantly longer in the 7 d reperfusion group compared with the sham operation group (Table 1).

Table 1: Effect of global cerebral I/R on spatial learning and memory in rats ().

Exploring time (s)

Day 1
Day 2
Day 3
Day 4
Day 5

Sham

I/R

Rats in I/R group were treated with global cerebral ischemia for 20 min, followed by reperfusion for 7 d. Dates are expressed as mean  SD of four individual experiments. ∗ ∗ compared with sham group.

3.3. Expression of PPARs, SOD2, and UCP2 mRNA and Protein

Global cerebral I/R significantly increased the expression of SOD2 mRNA in the rat hippocampus between 2 h and 15 d after I/R, with the peak expression at 48 h. The change of SOD2 protein levels in the rat hippocampus was similar to that of SOD2 mRNA expression, except that the peak time of expression was at 15 d (Figures 2(a) and 2(b)).

(a)

(b)

Figure 2: Time-dependent expression of SOD2 in global cerebral I/R rat hippocampus (). (a) The relative mRNA level of SOD2 was normalized to endogenous β-actin mRNA for each sample. (b) The relative protein level of SOD2 was normalized to endogenous β-actin protein for each sample. Dates are expressed as mean ± SD of four individual experiments. compared with sham group; compared with sham group.

Global cerebral I/R resulted in a significant increase of UCP2 mRNA expression in the rat hippocampus between 2 h and 15 d after I/R, with the peak expression at 48 h. Meanwhile, the UCP2 protein level in the rat hippocampus significantly increased from 6 h to 15 d, with the peak time of expression at 48 h (Figures 3(a) and 3(b)).

(a)

(b)

Figure 3: Time-dependent expression of UCP2 in global cerebral I/R rat hippocampus (). (a) The relative mRNA level of UCP2 was normalized to endogenous β-actin mRNA for each sample. (b) The relative protein level of UCP2 was normalized to endogenous β-actin protein for each sample. Dates are expressed as mean ± SD of four individual experiments. compared with sham group, compared with sham group.

Expression of PPARα mRNA in the rat hippocampus increased in the group with reperfusion for 30 min after global cerebral ischemia. However, there was no significant difference between the 30 min reperfusion group and sham operation group. After 2 h of reperfusion after global cerebral ischemia, PPARα mRNA expression in the rat hippocampus significantly increased compared with that of the sham operation group. At 24 h after I/R, PPARα mRNA expression reached the peak level, which was about 51% higher than that in the sham operation group ( versus ). Thereafter, PPARα mRNA expression began to decrease. The PPARα mRNA level at d 30 after I/R was only slightly higher than that in the sham operation group, with no significant difference between the two groups (Figure 4(a)).

(a)

(b)

Figure 4: Time-dependent expression of PPARα in global cerebral I/R rat hippocampus (). (a) The relative mRNA level of PPARα was normalized to endogenous β-actin mRNA for each sample. (b) The relative protein level of PPARα was normalized to endogenous β-actin protein for each sample. Dates are expressed as mean ± SD of four individual experiments. compared with sham group; compared with sham group.

The time-dependent course of PPARα protein expression in the rat hippocampus was similar to that of PPARγ mRNA expression. The peak time of PPARα protein expression was 24 h after I/R, and the peak concentration was about 63% higher than that in the sham operation group ( versus ) (Figure 4(b)).

I/R treatment significantly increased the expression of PPARβ mRNA in the rat hippocampus at 15 days after global cerebral ischemia and reperfusion, with the peak time of expression at 48 h. The level of PPARβ mRNA expression in the 48 h I/R-treated group was about 76% higher than that in the sham operation group ( versus ) (Figure 5(a)).

(a)

(b)

Figure 5: Time-dependent expression of PPARβ in global cerebral I/R rat hippocampus (). (a) The relative mRNA level of PPARβ was normalized to endogenous β-actin mRNA for each sample. (b) The relative protein level of PPARβ was normalized to endogenous β-actin protein for each sample. Dates are expressed as mean ± SD of four individual experiments. compared with sham group; compared with sham group.

The pattern of PPARβ protein expression was similar to that of PPARβ mRNA expression. The level of PPARβ protein expression in the 48 h I/R-treated group was about 65% higher than that in the sham operation group ( versus ) (Figure 5(b)). Compared with that of the sham operation group, PPARγ mRNA expression in the rat hippocampus of the I/R-treated group significantly increased, peaking at 24 h after I/R and then gradually decreased until finally approaching the control level at d 30. The peak concentration of PPARγ mRNA expression in the I/R-treated group was about 63% higher than that in the sham operation group ( versus ) (Figure 6(a)).

(a)

(b)

Figure 6: Time-dependent expression of PPARγ in global cerebral I/R rat hippocampus(). (a) The relative mRNA level of PPARγ was normalized to endogenous β-actin mRNA for each sample. (b) The relative protein level of PPARγ was normalized to endogenous β-actin protein for each sample. Dates are expressed as mean ± SD of four individual experiments. compared with sham group; compared with sham group.

The effect of global cerebral I/R on PPARγ protein expression in the rat hippocampus was similar to that of PPARγ mRNA expression, with the peak time of expression at 24 h after I/R. However, the peak concentration was about 101% higher than that in sham operation group ( versus ) (Figure 6(b)).

4. Discussion

By using immunohistochemistry and in situ hybridization, Braissant and Wahli found that PPARs (PPARα, β, and γ) show specific time- and tissue-dependent patterns of expression during fetal development in rodents and that the expression of PPARs regulates the development of CNS [21]. Moreno et al. [5] further studied the distribution of PPARs in the adult rat CNS and found that they are expressed in neurons of key brain regions such as the hippocampus and corpus striatum and that the expressed PPARs participate in motor and cognitive functions of the normal CNS and in corresponding dysfunctions in neurodegenerative pathologies. Recent studies showed that agonists of PPARs (PPARα, β, and γ) are protective against brain injury (i.e., ischemic cerebral damage and traumatic brain injury) and neurodegeneration (i.e., Alzheimer’s disease and Parkinson’s disease) [2, 22–24]. However, previous studies showed that the protective effects of PPAR agonists depend on the expression levels of the PPARs and their cofactors [19]. Therefore, it is necessary to clarify the time course of expression of PPARs in the cerebral hippocampus subjected to cerebral I/R injury.

In this study, our experimental results showed that the expression levels of PPARα, β, and γ mRNA and protein in hippocampi were significantly increased during 15 days after global cerebral I/R and peaked at 24 h for PPARα and γ and at 48 h for PPARβ. Although the time course of PPARα, β, and γ mRNA and protein expression in the hippocampus has not been reported in either the global or focal cerebral ischemia and reperfusion model, Zhao et al. previously found that in the peri-infarct cortical area of rats, the number of PPARγ immunoreactive cells dramatically increased 12 h after MCAO, then returned to basal values and remained unchanged until the end of the observation period of 7 days [15]. Victor et al. reported that PPARγ expression significantly increased between 4 h and 14 d and peaked at 24 h following MCAO [25]. Another previous study showed a persistent upregulation of PPARα-binding activity and protein expression in the injured human cerebral cortex 6–98 h after trauma brain injury, peaking between 24 and 72 h after injury [26].

Much evidence exists suggesting that effective neuroprotective compounds against ischemic cerebral injury require a wide therapeutic time window. In fact, in most cases, it is not clinically possible for drugs to be administered immediately after damage [27]. Considering that the protective effects of PPARs agonists depend on the expression levels of PPARs, our results showed that the peak time for PPARα, β, and γ expression was 24 h, 48 h, and 24 h, respectively, suggesting that administration of agonists against those molecules before those peak times after ischemia and reperfusion may be effective against ischemic brain injury. Zhao et al. found that treatment with RGZ improves behavioral functions even when first administered 24 h after embolic stroke and suggested that RGZ may potentially widen the therapeutic window of ischemic stroke [15]. Those results also partially support our hypothesis.

Mitochondrial uncoupling protein 2 (UCP2) is widely distributed in the rat brain including the hippocampus and is regarded as an important player in normal neuronal function as well as a key cell death suppression factor [28, 29]. Kainic acid has been shown to significantly upregulate UCP2 mRNA expression with the peak level at 24 h and returning to basal levels within 72 h after injection [30]. Lebedev and Arkhipov reported an increase in the level of UCP2 mRNA in the hippocampus one week after microinjection of kainic acid [31]. SOD2 is one of the most important antioxidative stress proteins. Previous studies have shown that transient global ischemia (TGI) can significantly increase expression of UCP2 and SOD2 in the hippocampal CA1 neurons 4–48 h after TGI [32]. In our study, global cerebral I/R could also significantly increase SOD2 and UCP2 mRNA and protein levels in the rat hippocampal CA1 tissue. Regarding the PPAR signaling pathways, it has been shown that local cerebral ischemic damage does not induce UCP2 mRNA in PPARβ knockout mice [10]. In other studies, TGI increased UCP2 expression in the mitochondria of hippocampal CA1 subfield 2–24 h after I/R, reaching peak levels at 6–18 h, while preadministration of RGZ to the hippocampus further enhanced mitochondrial UCP2 expression 2–6 h after I/R [33]. These results indicated that there is a PPARs-UCP2/SOD2 neuroprotection cascade in ischemic brain injury. Interestingly, our studies showed that the peak time of SOD2 mRNA is 48 h and the peak time of SOD2 protein is 15 d. The reason of the great time delay was unclear and was necessary to explore.

Moreover, our studies showed that although the expression levels of PPARs, SOD2, and UCP2 in the hippocampus were significantly induced, the rats still displayed obvious impairment of spatial learning and memory and obvious damage to the hippocampal neurons. These observations may be due to the increase of PPARs, SOD2, and UCP2 levels being insufficient to antagonize the damage caused by I/R. Therefore, exogenous PPARs agonists should be supplied. However, considering the fact that the transcriptional activity of PPARs and expression of co-factor LIM-only protein 4 (LMO4) are essential for ligand binding and receptor activation; in future studies, we will observe those levels at different times after cerebral I/R.

In conclusion, our experimental results indicate that global cerebral I/R can induce obvious increases of PPARα, β, and γ mRNA and protein expression 15 d after I/R, with peak expression times for PPARα, β, and γ at 24 h, 48 h, and 24 h, respectively. If confirmed, these results may help to guide the experimental and clinical use of PPARs agonists in the future.

Conflict of Interests

The authors declare no conflict of interests in this study.

Acknowledgments

This work was supported by Grants from the Natural Science Foundation of China (nos. 30672211, 81070972, and 81100905) and Chongqing Science Technology Commission of China (no. CSTC2011AC5203). The authors would like to thank Dr. T.-C. He of the University of Chicago Medical Center for his critical comments on the paper.

References

H. W. Liang, S. F. Qiu, J. Shen et al., “Genistein attenuates oxidative stress and neuronal damage following transient global cerebral ischemia in rat hippocampus,” Neuroscience Letters, vol. 438, no. 1, pp. 116–120, 2008.

R. Bordet, P. Gelé, P. Duriez, and J. C. Fruchart, “PPARs: a new target for neuroprotection,” Journal of Neurology, Neurosurgery and Psychiatry, vol. 77, no. 3, pp. 285–286, 2006.

F. Büttnera, C. Cordesb, F. Gerlachc et al., “Genomic response of the rat brain to global ischemia and reperfusion,” Brain Research, vol. 1252, pp. 1–14, 2009.

T. E. Cullingford, K. Bhakoo, S. Peuchen, C. T. Dolphin, R. Patel, and J. B. Clark, “Distribution of mRNAs encoding the peroxisome proliferator-activated receptor α, β, and γ and the retinoid X receptor α, β, and γ in rat central nervous system,” Journal of Neurochemistry, vol. 70, no. 4, pp. 1366–1375, 1998.

S. Moreno, S. Farioli-vecchioli, and M. P. Cerù, “Immunolocalization of peroxisome proliferator-activated receptors and retinoid X receptors in the adult rat CNS,” Neuroscience, vol. 123, no. 1, pp. 131–145, 2004.

L. Michalik, B. Desvergne, C. Dreyer, M. Gavillet, R. N. Laurini, and W. Wahli, “PPAR expression and function during vertebrate development,” International Journal of Developmental Biology, vol. 46, no. 1, pp. 105–114, 2002.

C. Blanquart, O. Barbier, J. C. Fruchart, B. Staels, and C. Glineur, “Peroxisome proliferator-activated receptors: regulation of transcriptional activities and roles in inflammation,” Journal of Steroid Biochemistry and Molecular Biology, vol. 85, no. 2–5, pp. 267–273, 2003.

Q. Guo, G. Wang, X. Liu, and S. Namura, “Effects of gemfibrozil on outcome after permanent middle cerebral artery occlusion in mice,” Brain Research C, vol. 1279, pp. 121–130, 2009.

M. Collino, M. Aragno, R. Mastrocola et al., “Oxidative stress and inflammatory response evoked by transient cerebral ischemia/reperfusion: effects of the PPAR-alpha agonist WY14643,” Free Radical Biology and Medicine, vol. 41, no. 4, pp. 579–589, 2006.

D. Arsenijevic, F. De Bilbao, J. Plamondon et al., “Increased infarct size and lack of hyperphagic response after focal cerebral ischemia in peroxisome proliferator-activated receptor β-deficient mice,” Journal of Cerebral Blood Flow and Metabolism, vol. 26, no. 3, pp. 433–445, 2006.

J. B. Pialat, T. H. Cho, O. Beuf et al., “MRI monitoring of focal cerebral ischemia in peroxisome proliferator-activated receptor (PPAR)-deficient mice,” NMR in Biomedicine, vol. 20, no. 3, pp. 335–342, 2007.

A. Iwashita, Y. Muramatsu, T. Yamazaki et al., “Neuroprotective efficacy of the peroxisome proliferator-activated receptor δ-selective agonists in vitro and in vivo,” Journal of Pharmacology and Experimental Therapeutics, vol. 320, no. 3, pp. 1087–1096, 2007.

Y. Q. Pan, J. Q. Yang, and R. C. Zhuang, “Effect of GW0742 on cerebral damage induced by global cerebral ischemia/reperfusion in rats,” Sichuan Journal of Zoology, vol. 28, no. 2, pp. 17–21, 2009.

M. P. Pereira, O. Hurtado, A. Cárdenas et al., “The nonthiazolidinedione PPARγ agonist L-796,449 is neuroprotective in experimental stroke,” Journal of Neuropathology and Experimental Neurology, vol. 64, no. 9, pp. 797–805, 2005.

Y. Zhao, A. Patzer, T. Herdegen, P. Gohlke, and J. Culman, “Activation of cerebral peroxisome proliferator-activated receptors gamma promotes neuroprotection by attenuation of neuronal cyclooxygenase-2 overexpression after focal cerebral ischemia in rats,” FASEB Journal, vol. 20, no. 8, pp. 1162–1175, 2006.

S. Ji, G. Kronenberg, M. Balkaya et al., “Acute neuroprotection by pioglitazone after mild brain ischemia without effect on long-term outcome,” Experimental Neurology, vol. 216, no. 2, pp. 321–328, 2009.

K. J. Lee, Y. H. Jang, H. Lee, H. S. Yoo, and S. R. Lee, “PPARγ agonist pioglitazone rescues neuronal cell damage after transient global cerebral ischemia through matrix metalloproteinase inhibition,” European Journal of Neuroscience, vol. 27, no. 2, pp. 334–342, 2008.

M. Allahtavakoli, R. Moloudi, M. K. Arababadi, A. Shamsizadeh, and K. Javanmardi, “Delayed post ischemic treatment with Rosiglitazone attenuates infarct volume, neurological deficits and neutrophilia after embolic stroke in rat,” Brain Research C, vol. 1271, pp. 121–127, 2009.

S. C. Schock, J. Xu, P. M. Duquette et al., “Rescue of neurons from ischemic injury by peroxisome proliferator-activated receptor-γ requires a novel essential cofactor LMO4,” Journal of Neuroscience, vol. 28, no. 47, pp. 12433–12444, 2008.

R. J. Traystman, “Animal models of focal and global cerebral ischemia,” ILAR Journal, vol. 44, no. 2, pp. 85–95, 2003.

O. Braissant and W. Wahli, “Differential expression of peroxisome proliferator-activated receptor- α, -β, and -γ during rat embryonic development,” Endocrinology, vol. 139, no. 6, pp. 2748–2754, 1998.

V. C. Besson, X. R. Chen, M. Plotkine, and C. Marchand-Verrecchia, “Fenofibrate, a peroxisome proliferator-activated receptor α agonist, exerts neuroprotective effects in traumatic brain injury,” Neuroscience Letters, vol. 388, no. 1, pp. 7–12, 2005.

M. T. Heneka and G. E. Landreth, “PPARs in the brain,” Biochimica et Biophysica Acta, vol. 1771, no. 8, pp. 1031–1045, 2007.

M. Collino, N. S. A. Patel, and C. Thiemermann, “Review: PPARs as new therapeutic targets for the treatment of cerebral ischemia/reperfusion injury,” Therapeutic Advances in Cardiovascular Disease, vol. 2, no. 3, pp. 179–197, 2008.

N. A. Victor, E. W. Wanderi, J. Gamboa et al., “Altered PPARγ expression and activation after transient focal ischemia in rats,” European Journal of Neuroscience, vol. 24, no. 6, pp. 1653–1663, 2006.

D. Feng, Y. Zhang, and G. Chen, “Cortical expression of peroxisome proliferator-activated receptor-α after human brain contusion,” Journal of International Medical Research, vol. 36, no. 4, pp. 783–791, 2008.

A. R. Green and A. Shuaib, “Therapeutic strategies for the treatment of stroke,” Drug Discovery Today, vol. 11, no. 15-16, pp. 681–693, 2006.

I. Bechmann, S. Diano, C. H. Warden, T. Bartfai, R. Nitsch, and T. L. Horvath, “Brain mitochondrial uncoupling protein 2 (UCP2): a protective stress signal in neuronal injury,” Biochemical Pharmacology, vol. 64, no. 3, pp. 363–367, 2002.

T. L. Horvath, S. Diano, and C. Barnstable, “Mitochondrial uncoupling protein 2 in the central nervous system: neuromodulator and neuroprotector,” Biochemical Pharmacology, vol. 65, no. 12, pp. 1917–1921, 2003.

S. Clavel, E. Paradis, D. Ricquier, and D. Richard, “Kainic acid upregulates uncoupling protein-2 mRNA expression in the mouse brain,” Neuroreport, vol. 14, no. 16, pp. 2015–2017, 2003.

D. S. Lebedev and V. I. Arkhipov, “Expression of mitochondrial uncoupling protein UCP2 in the brain of rats after hippocampal injury inflicted by kainic acid,” Bulletin of Experimental Biology and Medicine, vol. 150, no. 2, pp. 185–187, 2010.

S. D. Chen, T. K. Lin, D. I. Yang et al., “Protective effects of peroxisome proliferator-activated receptors γ coactivator-1α against neuronal cell death in the hippocampal CA1 subfield after transient global ischemia,” Journal of Neuroscience Research, vol. 88, no. 3, pp. 605–613, 2010.

S. D. Chen, H. Y. Wu, D. I. Yang et al., “Effects of rosiglitazone on global ischemia-induced hippocampal injury and expression of mitochondrial uncoupling protein 2,” Biochemical and Biophysical Research Communications, vol. 351, no. 1, pp. 198–203, 2006.