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Development of telmisartan in the therapy of spinal cord injury: pre-clinical study in rats

Authors Lin C, Tsai J, Chang CK, Cheng J, Lin J

Received 14 April 2015

Accepted for publication 13 May 2015

Published 14 August 2015 Volume 2015:9 Pages 4709—4717

DOI https://doi.org/10.2147/DDDT.S86616

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Professor Shu-Feng Zhou

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Chien-Min Lin,1,* Jo-Ting Tsai,2,* Chen Kuei Chang,1 Juei-Tang Cheng,3 Jia-Wei Lin1

1
Department of Neurosurgery, 2Department of Radiation Oncology, Shuang Ho Hospital-Taipei Medical University, 3Institute of Medical Science, College of Health Science, Chang Jung Christian University, Tainan City, Taiwan

*These authors contributed equally to this work

Background: Decrease of peroxisome proliferator-activated receptors-δ (PPARδ) expression has been observed after spinal cord injury (SCI). Increase of PPARδ may improve the damage in SCI. Telmisartan, the antihypertensive agent, has been mentioned to increase the expression of PPARδ. Thus, we are going to screen the effectiveness of telmisartan in SCI for the development of it in clinical application.
Methods: In the present study, we used compressive SCI in rats. Telmisartan was then used to evaluate the influence in rats after SCI. Change in PPARδ expression was identified by Western blots. Also, behavioral tests were performed to check the recovery of damage.
Results: Recovery of damage from SCI was observed in telmisartan-treated rats. Additionally, this action of telmisartan was inhibited by GSK0660 at the dose sufficient to block PPARδ. However, metformin at the dose enough to activate adenosine monophosphate-activated protein kinase failed to produce similar action as telmisartan. Thus, mediation of adenosine monophosphate-activated protein kinase in this action of telmisartan can be rule out. Moreover, telmisartan reversed the expressions of PPARδ in rats with SCI.
Conclusion: The obtained data suggest that telmisartan can improve the damage of SCI in rats through an increase in PPARδ expression. Thus, telmisartan is useful to be developed as an agent in the therapy of SCI.

Keywords: PPARδ, AMPK, spinal cord injury, angiotensin receptor blocker, metformin

Introduction

Spinal cord injury (SCI) is defined as a damage to the spinal structure and/or function that can be caused by a host of etiological factors, including labor injuries and traffic accidents; the condition also creates enormous physical and emotional cost to individuals.1 SCI easily leads to motor paralysis and sensory dysfunction while both afferent sensory and efferent motor innervations are passing through the spinal cord.2 The sensory dysfunction is associated with urinary impairment, which is a major factor in morbidity and even mortality in those with SCI.3

Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily, which includes the classical steroid, thyroid, and retinoid hormone receptors.4 At present, three PPAR subtypes have been identified to be designed as PPARα, PPARδ, and PPARγ.5 PPARs are involved in the pathogenesis of several diseases, including diabetes mellitus, obesity, atherosclerosis, neurological diseases, and SCI.68 It has been documented that GW0742 (a selective agonist of PPARδ) can reduce the development of inflammation and tissue injury associated with SCI.9 However, application of useful medication in patients with SCI is still not enough.

Angiotensin II (Ang II) receptor blockers (ARBs) are commonly used to lower the blood pressure.10 In addition to antihypertensive effect, several clinical trials show that ARBs have some effects on energy metabolism.11 The pleiotropic effects of ARBs include the upregulation of uncoupling protein 1 or Ang II receptor type 1 expression and the activation of PPAR.12 Recently, telmisartan, one of the ARBs, has been found to increase the expressions of PPARδ and adenosine monophosphate-activated protein kinase (AMPK) in skeletal muscle of rats.13 Additionally, the activation of PPARδ is helpful to improve the injury from SCI in diabetic rats.14 The present study is thus designed to investigate the therapeutic potential of telmisartan in SCI using animal model as pre-clinical evidence.

Materials and methods

Experimental animals

The male Wistar rats obtained from the animal center of National Cheng Kung University Medical College (Tainan, Taiwan) were maintained in a temperature-controlled room (25°C±1°C) under a 12-hour light–dark cycle (lights on at 06 am). All rats received water and standard chow (Purina Mills, LLC, St Louis, MO, USA) ad libitum. All animal-handling procedures were performed according to the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health and followed the guidelines of the Animal Welfare Act.

Spinal cord injury

We performed the SCI mainly according to our previous method15 with some modifications.16 In brief, the laminectomy for removal of the vertebral peduncle was performed between T8 and T9 on rats under anesthesia with sodium pentobarbital (30 mg/kg, intraperitoneally; Sigma Chemical Co, St Louis, MO, USA). We used a calibrated aneurysm clip with a closing pressure of 55 g to place between the dorsal and ventral surfaces of spinal cord for 1 minute. Animals that received the same laminectomy without compression with clip were grouped as the sham-operated control. Then, we injected 0.1 mL of cefazolin (10 mg/kg body weight; China Chemical Pharmaceutical Co, Ltd, Taipei, Taiwan) into all animals for 3 days after the surgery. Animals that received SCI were individually housed on a special bedding to prevent the formation of pressure sores. Additionally, rats had their bowel and bladder manually compressed twice daily. Food and water were supplied at a lowered height in their cages for free accessibility.15 Similar to the previous report,15 the rats typically did not survive beyond 4–5 weeks after the SCI. In the present study, telmisartan, metformin and GSK0660 (a selective antagonist of PPARδ) purchased from Tocris Bioscience (Ellisville, MO, USA) were dissolved in dimethyl sulfoxide and diluted with saline. The oral solution of metformin (320 mg/kg),17 telmisartan (5 mg/kg),13,18 and/or GSK0660 (0.1 mg/kg)14 was intravenously injected into the rats via tail vein for 20 days after 1 week of SCI every morning (10 am). Additionally, we employed the vehicle at the same volume to treat the control group in the same manner. The behavioral test took place every Monday evening (6 pm) after 1 week of drug administration. The rats that cannot survive until the end of this study (28 days) were excluded. The results were obtained from each group of six rats for further analysis.

Locomotor scale

According to the earlier report,19 the Basso, Beattie and Bresnahan (BBB) locomotor rating scale (locomotor scale) from 0 to 21, where 0 reflects no locomotor function and 21 reflects normal performance, is used to evaluate the effects of metformin (320 mg/kg),17 telmisartan (5 mg/kg),13 and/or GSK0660 (0.1 mg/kg)14 on functional recovery after SCI. We arranged the rats to walk around freely in a 90 cm2 field (width and length) for 4 minutes, and movements of the hind limb were observed continuously. Rats were trained to gently adapt to the field at first. Two investigators conducted 4-minute testing sessions on each leg of the rats that walked continuously in the field. This study started one day postinjury and continued for 20 days or over. The functional deficits were double-blind checked by the trained investigators. The results of behavior outcomes and examples of locomotor scores were also recorded in the digital video.

Inclined plane test

We applied the inclined plane test (IPT) to evaluate the ability of rats to maintain their position for 5 seconds on an inclined plane that was covered with a rubber mat containing horizontal ridges (1 mm deep, spaced 3 mm apart, and self-made), as described previously.20 The rats were determined as the angle of the surface was increased from 5° to 90° at 5° intervals. The angle at which the rat could not maintain its position was the outcome measured.

Limb hanging test

This test is used for evaluating both forelimb and hind limb function. However, it is mainly employed for testing muscle function in the forelimbs of animals with SCI, as mentioned in previous reports.21 The test is conducted using a 12 cm long and 1.8 mm wide rounded metal rod that is applied to the volar surface of the forepaw, and the presence or absence of grasping and the release time in seconds are recorded. When the rod is lifted above the surface and suspended, the testing of animal’s forelimb muscle strength is possible. In addition, contact of the body, hind limb, or tail with the ground or parts of the equipment on the sides should be prevented. The time that the rat hangs suspended on the rod is measured and recorded. This testing should typically be repeated five times. The mean values of each administration were calculated, as described previously.21

Pain test

All rats were adapted to testing chambers for at least 2 days. The occurrence of foot withdrawal in response to the mechanical notching of the plantar surface of each hind paw was measured using a flat-tipped cylindrical probe that measured 200 μm in diameter, following previous methods.22 Von Frey filaments capable of exerting forces with a uniform tip diameter were applied to a designated loci on the plantar surface of the foot. During each experiment, the rat was placed in an obvious plastic cage with a floor of wire with approximately 1 cm2 openings. The cage was elevated so that stimulation was practical for each hind foot from underneath the rodent. The duration of each stimulus was approximately 1 second, and the interstimulus interval was approximately 10–15 seconds. The force unit was expressed in Newtons (N).

Western blotting analysis

Spinal cord tissues were isolated from all the six rats in each group treated with telmisartan and/or GSK0660, and metformin after SCI. Tissues were homogenized in the ice-cold buffer solution containing 10 mM Tris-HCl (pH 7.4), 20 mM ethylenediaminetetraacetic acid, 10 mM ethylene glycol tetraacetic acid, 20 mM β-glycerophosphate, 50 mM NaF, 50 mM sodium pyrophosphate, 1 mM phenylmethylsulfonyl fluoride, and the protease inhibitors 25 μg/mL leupeptin and 25 μg/mL aprotinin. The mixture was then centrifuged at 1,000× g for 10 minutes. The obtained supernatant was further centrifuged at 48,000× g for 30 minutes. After resuspension of the pellet in ice-cold Triton X-100 lysis buffer, samples were centrifuged at 14,010× g for 20 minutes. All the above centrifugations were performed at 4°C. The supernatant was collected in an Eppendorf tube to store at -80°C. The membrane extracts (20–80 μg) in the supernatant were applied for separation using 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The obtained proteins were transferred onto a BioTrace™ polyvinylidene fluoride membrane (Pall Corporation, Pensacola, FL, USA) for 2 hours. The blots were developed through the reaction with primary antibodies (1:1,000) of receptor for advanced glycation endproducts (RAGE), high-mobility group box 1 protein (HMGB1), phosphorylated AMPK (p-AMPK), PPARδ, and actin (Abcam, Cambridge, UK) for 16 hours. Then, they were hybridized with horseradish peroxidase-conjugated rabbit anti-rabbit IgG (Jackson ImmunoResearch Laboratories, Inc, PA, USA) for 2 hours and developed with the Western Lightning Chemiluminescence Reagent PLUS (PerkinElmer Life Sciences Inc., Boston, MA, USA). We employed Gel-Pro analyzer software 4.0 (Media Cybernetics, Silver Spring, MD, USA) to quantify the densities of the obtained immunoblots at 35 KDa for RAGE, 29 KDa for HMGB1, 62 KDa for p-AMPK, 40 KDa for PPARδ, and 43 KDa for actin, respectively.

Statistical analysis

All results were expressed as the mean ± standard error of each group. Statistical analysis was performed using analysis of variance with the Newman–Keuls post-hoc. A P-value of ≤0.05 was considered statistically significant.

Results

Effects of telmisartan on motor function and pain response in rats with SCI

Overground locomotion using the BBB scoring system showed consistent weight support and consistent forelimb–hindlimb coordination.23 As shown in Figure 1A, telmisartan improved the BBB locomotor scale in rats with SCI.

Figure 1 Changes in behavioral and pain tests in rats with SCI after receiving telmisartan and/or GSK0660.
Notes: The rats with SCI were treated with telmisartan (5 mg/kg) and/or GSK0660 (0.1 mg/kg) intravenously once daily for 28 days. Tests showed (A) BBB locomotor scale, (B) inclined plane test, (C) limb hanging test, and (D) pain test. Values (mean ± SE) were obtained from each group of six rats. *P<0.05, **P<0.01 and ***P<0.001 compared with the vehicle-treated SCI rats.
Abbreviations: BBB, Basso, Beattie and Bresnahan; GSK, glycogen synthase kinase; SCI, spinal cord injury; SE, standard error.

The inclined plane evaluates the ability of the animal to maintain its body position on a surface that is gradually raised to increasing angles. In the rat models of SCI, this test has been shown reliable, consistent, and sensitive and that has been used to assess the therapeutic modalities.24 As shown in Figure 1B, telmisartan improved the behaviors including the result of IPT in rats with SCI.

Limb hanging wire test evidenced a reduction of muscle strength in rats.25 As shown in Figure 1C, telmisartan improved the results of limb hanging test in rats with SCI.

Pain test evaluates the nociceptive mechanical threshold. As shown in Figure 1D, telmisartan decreased the mechanical threshold in rats with SCI.

As shown in Figure 1, telmisartan combined injection of GSK0660 (0.1 mg/kg, once daily) to these rats that attenuated the improvements of motor function and pain responses induced by telmisartan.

Effects of telmisartan on PPARδ and p-AMPK expressions in rats with SCI

After evaluating the behavioral tests, we used the spinal cord from each rat in the same group to perform the Western blotting analysis. As shown in Figure 2, the PPARδ and p-AMPK expressions in spinal cord of SCI rats were markedly lower than that in normal rats. The expressions of PPARδ and p-AMPK were both reversed by telmisartan in rats with SCI. This action of telmisartan was attenuated by GSK0660 at an effective dose to block PPARδ as described previously.13 However, metformin failed to modify the expression of PPARδ in rats with SCI.

Figure 2 The expressions of PPARδ and p-AMPK in spinal cord of rats with SCI after treatment with metformin, telmisartan and/or GSK0660.
Notes: The rats with SCI were treated with metformin (320 mg/kg), telmisartan (5 mg/kg) and/or GSK0660 (0.1 mg/kg) intravenously once daily for 28 days. Expressions of PPARδ (A) and p-AMPK (B) were identified using Western blotting analysis. Protein expression was normalized against that of β-actin used as a loading control. Data represent the mean ± SEM of six animals. ***P<0.001 compared with the vehicle-treated SCI rats.
Abbreviations: AMPK, adenosine monophosphate-activated protein kinase; GSK, glycogen synthase kinase; p-AMPK, phosphorylated AMPK; PPAR, Peroxisome proliferator-activated receptors; SCI, spinal cord injury; SEM, standard error of mean.

Metformin failed to improve the motor function and pain response in rats with SCI

As shown in Figure 3, metformin failed to improve the behaviors in rats with SCI including the BBB locomotor scale, IPT, limb hanging test and pain test. The treated dose of metformin is enough to increase p-AMPK in these rats as shown in Figure 2B.

Figure 3 Changes of behavioral and pain tests in rats with SCI by metformin.
Notes: The rats receiving SCI was further treated with metformin (320 mg/kg) intravenously once daily for 28 days. Responses show (A) BBB locomotor scale, (B) inclined plane test, (C) limb hanging test, and (D) pain test. Values (mean ± SE) were obtained from each group of six rats. Each group compared with the vehicle-treated SCI rats without statistical difference.
Abbreviations: BBB, Basso, Beattie and Bresnahan; SCI, spinal cord injury; SE, standard error.

Effects of telmisartan on HMGB1 and RAGE expressions in rats with SCI

PPARδ has been indicated to show anti-inflammatory effects in neurological and inflammatory-related diseases.26 As shown in Figure 4, the inflammatory indicators, HMGB1 and RAGE expressions, in the spinal cords of rats with SCI were markedly higher than that in normal rats. The expression of HMGB1 (Figure 4A) or RAGE (Figure 4B) was reversed by telmisartan in rats with SCI. This action of telmisartan was also attenuated by GSK0660. Additionally, as shown in Figure 4, metformin failed to modify the expressions of HMGB1 and RAGE in rats with SCI.

Figure 4 The expressions of HMGB1 and RAGE in spinal cord from rats with SCI after treatment with metformin, telmisartan and/or GSK0660.
Notes: The rats with SCI were treated with metformin (320 mg/kg), telmisartan (5 mg/kg) and/or GSK0660 (0.1 mg/kg) intravenously once daily for 28 days. Expressions of (A) HMGB1 and (B) RAGE were identified using Western blotting analysis. Protein expression was normalized against that of β-actin used as a loading control. Data represent the mean ± SEM of six animals. **P<0.01 and ***P<0.001 compared with the vehicle-treated SCI rats.
Abbreviations: GSK, glycogen synthase kinase; HMGB1, high-mobility group box 1 protein; RAGE, receptor for advanced glycation endproducts; SCI, spinal cord injury; SEM, standard error of mean.

Discussion

In the present study, we found that the motor dysfunction and pain responses were improved by telmisartan in rats with SCI. This action of telmisartan was inhibited by a blockade of PPARδ. PPARδ expression was not reduced after SCI in rats treated with telmisartan. Moreover, the expression of p-AMPK was also raised by telmisartan. Metformin at the dose enough to activate AMPK failed to modify the motor dysfunction and pain responses in rats with SCI. The therapeutic potential of telmisartan in rats with SCI is mainly through the restoration of PPARδ expression.

Recently, the pharmacological activation of PPARδ has been considered as the potential target due to its anti-inflammatory/antioxidant/anti-excitotoxic/pro-energetic profile in some neurological and inflammatory-related diseases.26 PPARδ has also drawn much attention as a drug discovery target for regulating glucose and lipid metabolism27 because PPARs are widely distributed throughout the body and are mainly known for their effects on metabolism. Three isoforms of PPARs have been identified as PPARα, PPARδ (also called PPARβ), and PPARγ.28 PPARα and PPARγ are involved in the metabolism of lipid and glucose. Basically, PPARδ is the most abundant PPAR isoform in the body and many studies have demonstrated its role in antioxidative stress29 and neuroprotection.30 Moreover, decrease of PPARδ delayed the recovery of motor behaviors in animals with SCI, which was related to a reduced ability to repair the injured tissue and to recover the neurological functions.31 As shown in Figures 1 and 2, rats with SCI showed poor motor behaviors than normal rats while the expression of PPARδ in spinal cord was also decreased. Our results are consistent with the previous report9 showing the usefulness of this animal model.

Selective β1-adrenoceptor antagonists have demonstrated a reduction in neurological injury in a rat model of spinal cord ischemia-reperfusion under its’ effective dosage for treating hypertension.32 Additionally, calcium channel blocker has been identified to ameliorate the disease in a mouse model of multiple sclerosis.33

ARBs are also widely used for the treatment of hypertension in clinics. By blocking type-1 Ang II receptors, ARBs not only ameliorate hypertension but also inhibit the Ang II-stimulated induction of profibrotic cytokines and oxidative stress, thereby retarding the progression of chronic renal parenchymal injury.34 Some ARBs have also been shown to act as activators of PPAR and consequently induce anti-inflammatory effects by interfering with inflammatory signaling.35 Telmisartan, one of ARBs, has recently been attracting attention due to its putative PPARδ action13 and ensuing anti-inflammatory effects.36,37 Previous report also indicated that telmisartan can activate the PPARδ and increase the p-AMPK.13 However, the effect of ARBs in SCI is still unclear. Thus, we employed the same dose of telmisartan13 in our investigation in the present study.

In the central nervous system, PPARδ is expressed mainly in oligodendrocytes and neurons.38 Activation of PPARδ reduced the cellular and molecular changes occurring in SCI by targeting different downstream pathways, thereby modulating PPARδ receptors.39 Also, this protective effect is significantly blocked by GSK0660.9 Comparable results were observed in the present study using rats with SCI, in which the PPARδ expression and behavioral responses were both improved by telmisartan (Figures 1 and 2).

To evaluate the effects of motor function and pain responses in rats after SCI, several behavioral tests were applied, including the BBB locomotor scale, IPT, and limb hanging test.24,40,41 The motor functions in diabetic rats can be influenced after SCI by the pharmacological manipulation of PPARδ activity, as described earlier.9 As shown in Figure 1, an activation of PPARδ by telmisartan improved the motor dysfunction and increased pain sensitivity. Additionally, the blockade of PPARδ using GSK0660 reversed these actions of telmisartan. Thus, PPARδ is mediated in the telmisartan-induced recovery of damage in rats with SCI. It is also observed that PPARδ is highly expressed in the central nervous system,42 with a great influence on neuronal cell functioning.43 Thus, we identified the changes of PPARδ expression by telmisartan in rats with SCI. As shown in Figure 2, PPARδ expression in spinal cords of these rats was markedly increased by telmisartan; this result is consistent with a previous reporton skeletal muscle.13 Our data shows that an activation of PPARδ by telmisartan is helpfulin improving the injury from SCI in rats. However, more investigations are required in the future for understanding the molecular action mechanism(s) of PPARδ in SCI.

Metformin has widely been used to treat type-2 diabetes patients.4448 The key molecular mechanism of metformin is introduced to produce an activation of AMPK.36 A previous report has indicated that telmisartan can enhance the phosphorylation of AMPK through increased PPARδ expression.13 It is similar to the present study using rats with SCI. However, the benefit of AMPK activation in the recovery of SCI is still obscure. In the present study, we used metformin as positive reference to test the role of p-AMPK in rats with SCI. The data showed that metformin failed to improve the motor behaviors (Figure 3) in SCI rats although it increased the expression of p-AMPK (Figure 2) similar to telmisartan. Metformin (the AMPK activator) treatment may not activate all the necessary factors and cofactors that mediate recovery in this compressive SCI model. Thus, mediation of AMPK seems not to be the major factor in the action of telmisartan for improvement of SCI in rats.

It has been indicated that ARBs inhibit the HMGB1/RAGE axis49 to benefit patients with stroke.50 The extracellular release of HMGB1 appears to be common to the etiology and progression of multiple diseases leading to stroke, and may act in a multistage process in stroke.51 Inhibition of the HMGB1/RAGE axis may prove to be a novel therapeutic strategy for treating stroke.52 This action was not related to the change of blood pressure by ARBs.52 Thus, it seems there is no correlation of SCI improvement and hypotensive effects in rats. Additionally, it has been demonstrated that activation of PPARγ inhibits the HMGB1–RAGE pathway.53,54 In the present study, we are the first to demonstrate that blockade of PPARδ using GSK0660 can inhibit the telmisartan-induced changes of HMGB1 and RAGE expressions. However, the underlying mechanisms need more investigations in the future.

Conclusion

We found that telmisartan is effective in improving the motor behaviors in rats with compressive SCI through an increased expression of PPARδ and a marked reduction in the expressions of HMGB1 and RAGE in spinal cords. In the current study, the therapeutic potential of telmisartan in SCI is addressed for the first time. However, more studies on the different models of SCI should be conducted in the future.

Acknowledgments

We thank Pei-Lin Chou and Yi-Zhi Chen for their assistance in our experiments.

Disclosure

The authors report no conflicts of interest in this work.


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