Pretreatment with Danhong injection protects the brain against ischemia-reperfusion injury

Shaoxia Wang, Hong Guo, Xumei Wang, Lijuan Chai, Limin Hu, Tao Zhao, Buchang Zhao, Xiaoxu Tan, Feifei Jia

1 Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China

2 Tianjin Key Laboratory of Chinese Medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin, China

3 Buchang Pharmaceutical Co., Ltd., Xi’an, Shaanxi Province, China

Pretreatment with Danhong injection protects the brain against ischemia-reperfusion injury

Shaoxia Wang1, Hong Guo2, Xumei Wang1, Lijuan Chai1, Limin Hu1, Tao Zhao3, Buchang Zhao3, Xiaoxu Tan2, Feifei Jia2

1 Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China

2 Tianjin Key Laboratory of Chinese Medicine Pharmacology, Tianjin University of Traditional Chinese Medicine, Tianjin, China

3 Buchang Pharmaceutical Co., Ltd., Xi’an, Shaanxi Province, China

Danhonginjection (DHI), a Chinese Materia Medica standardized product extracted fromRadix Salviae miltiorrhizaeandFlos Carthami tinctorii, is widely used in China for treating acute ischemic stroke. In the present study, we explored the neuroprotective ef fi cacy of DHI in a rat model of temporary middle cerebral artery occlusion, and evaluated the potential mechanisms underlying its effects. Pretreatment with DHI (0.9 and 1.8 mL/kg) resulted in a signi fi cantly smaller infarct volume and better neurological scores than pretreatment with saline. Furthermore, DHI significantly reduced the permeability of the blood-brain barrier, increased occludin protein expression and decreased neutrophil in fi ltration, as well as profoundly suppressing the upregulation of matrix metallopeptidase-9 expression seen in rats that had received vehicle. Matrix metallopeptidase-2 expression was not affected by ischemia or DHI. Moreover, DHI (1.8 mL/kg) administered 3 hours after the onset of ischemia also improved neurological scores and reduced infarct size. Our results indicate that the neuroprotective ef fi cacy of DHI in a rat model of cerebral ischemia-reperfusion injury is mediated by a protective effect on the blood-brain barrier and the reversal of neutrophil in fi ltration.

nerve regeneration; Danhong injection; Radix Salviae Miltiorrhiae; Flos Carthami; cerebral ischemia-reperfusion; neutrophil infiltration; matrix metallopeptidase; blood-brain barrier; NSFC grant; neural regeneration

Funding:This study was supported by the National Natural Science Foundation of China, No. 81173592; National Science and Technology Major Project of the Ministry of Science and Technology of China, No. 2011ZX09201-201, 2012ZX09101201-004, 2012ZX09101202, NCET-13-0935, 2013ZX09201020; Tianjin Municipal Applied Basic Research and Cutting-Edge Technology Research Scheme of China, No. 14JCYBJC28900; and Program for Innovation Team Training in Universities in Tianjin, No. TD12-5035.

Wang SX, Guo H, Wang XM, Chai LJ, Hu LM, Zhao T, Zhao BC, Tan XX, Jia FF. Pretreatment with Danhong injection protects the brain against ischemia-reperfusion injury. Neural Regen Res. 2014;9(15)：1453-1459.

Introduction

Over the past few decades, hundreds of neuroprotective agents have reached clinical trials of ischemic stroke (Ginsberg, 2008; Turner et al., 2013). However, thrombolytic therapy with intravenous tissue plasminogen activator remains the only US Food and Drug Administration-approved treatment for acute ischemic stroke since 1996 (Matsuo et al., 2013). But its narrow therapeutic window and risks of cerebral hemorrhage limit its widespread application (De Keyser et al., 2005). Therefore, the development of a new drug for stroke remains an urgent priority.

In contrast with western developed countries, China has many herbal preparations for the clinical treatment of acute ischemic stroke.Danhonginjection (DHI) is a Chinese Materia Medica standardized product extracted fromRadix Salviae miltiorrhizaeandFlos Carthami tinctorii(Li et al., 2011; Liu et al., 2013). Both of these are traditional Chinese herbs widely used in the treatment of cerebrovascular disorders and coronary artery disease (Zhou et al., 2005; Sun et al., 2009).e main components of this preparation have been identi fi ed in previous studies from our research group (Liu et al., 2013). DHI containsdanshensu(tanshinol); salvianolic acids A, B, and C; rosmarinic acid; protocatechuic acid; and saccharides.e pharmacologic activities of these components have been extensively documented. For example, salvianolic acid B inhibits platelet aggregation (Ma et al., 2011), ameliorates microcirculatory disturbance (Han et al., 2008), and has anti-inflammatory (Wang et al., 2010) and anti-oxidant properties (Zhao et al., 2008; Wang et al., 2010). Salvianolic acid B also exerts neuroprotective e ff ects against Aβ neurotoxicity (Lee et al., 2013) and traumatic brain injury (Chen et al., 2011)in vivo. Salvianolic acid A has similar activities (Ho and Hong, 2011).Danshensuis an anti-oxidant (Zhao et al., 2008), inhibits nuclear factor-κB expression (Jiang et al., 2013), and protects endothelial cells (Yang et al., 2010). It also suppresses cardiomyocyte apoptosis and provides significant cardioprotection against myocardial ischemia and reperfusion injury by activating the PI3K/Akt andERK1/2 signaling pathways (Yin et al., 2013). Rosmarinic acid was also proposed as a potential cardiovascular drug in a recent review (Ferreira et al., 2013). Growing evidence suggests that rosmarinic acid alleviates diabetic cerebral ischemia-reperfusion injury and attenuates blood-brain barrier (BBB) breakdownviahigh mobility group box-1 protein and the nuclear factor-κB signaling pathway (Luan et al., 2013).e combined e ff ects of the individual components are the basis of the neuroprotective e ff ects of DHI.

Figure 1 Effect ofDanhonginjection (DHI) pretreatment on infarct volume and neurological de fi cit in rats after middle cerebral artery occlusion.

In the present study, we con fi rm the neuroprotective e fficacy of DHI in a rat model of cerebral ischemia-reperfusion injury, and evaluate the potential mechanisms underlying this process.

Materials and Methods

Establishment of cerebral ischemia-reperfusion model

Figure 2 Effect ofDanhonginjection (DHI) on blood-brain barrier permeability and expression of occludin protein in rats after middle cerebral artery occlusion.

A total of 92 adult male Wistar rats (weighing 250-280 g; speci fi c pathogen-free grade; license No. SCXK (Jing) 2012-0001; Vital River, Beijing, China) were used. Rats were housed five per cage at a stable temperature (22 ± 0.5°C) under a 12 hour light/dark cycle (lights on at 07：00) and had free access to standard rat chow and water. All procedures were approved by the Animal Care and Use Committee at Tianjin University of Traditional Chinese Medicine in China.

The rats were divided into six groups： sham (n= 14), model (n= 23), 0.9 mL/kg DHI (n= 8), 1.8 mL/kg DHI (n= 24), post-treatment model (n= 11) and post-treatment DHI (n= 12). Anesthesia was induced with chloral hydrate (10%, 3 mL/kg). All groups except sham underwent middle cerebral artery occlusion surgery as previously described (Wang et al., 2012). Brie fl y, the left common carotid artery was exposed and a silicon-coated 4-0 nylon filament was introduced into the left internal carotid artery through the common carotid artery. Sixty minutes after middle cerebralartery occlusion, the intraluminal suture was withdrawn. For the sham group, we cut an incision and closed it without occlusion of the artery. Laser Doppler (Perimed, Jarfalla, Sweden) was used to monitor cerebral blood flow during the procedure to con fi rm occlusion. Body temperature was monitored by a rectal probe and maintained at 37°C using a feedback-regulated heating system (CMA/Microdialysis AB, Knivsta, Sweden) during surgery.

Figure 3 Effect ofDanhonginjection (DHI) on myeloperoxidase (MPO) expression in rat brain after middle cerebral artery occlusion.

Drug treatment

DHI was provided by Buchang Pharmaceutical Co., Ltd. (lot No. 130932, 10 mL/vial, Xi’an, Shaanxi Province, China). Quantitative analysis of its components was conducted using high performance liquid chromatography (Waters Corp., Milford, MA, USA) as described previously (He et al., 2012; Liu et al., 2013).

For DHI pretreatment, rats in the DHI groups received a single intraperitoneal injection of DHI (0.9 mL/kg or 1.8 mL/kg) 30 minutes before surgery, and then once daily for 3 additional days. In the sham and model groups, rats received saline (1 mL/200 g) only.

For DHI post-treatment, the first treatment with DHI (1.8 mL/kg) was given 3 hours after the onset of ischemia, and then once daily for 3 subsequent days.

Neurological de fi cits

The Bederson scale was used to assess general neurological status (Bederson et al., 1986). Tests were performed at 24 and 72 hours after surgery and scored as follows： 0, no observable de fi cit; 1, forelimb fl exion; 2, decreased resistance to lateral push without circling; 3, same behavior as 2 but with circling; 4, ambulation dif fi culty or inability.

Assessment of cerebral infarct size by TTC staining

After 72 hours of reperfusion, the rats were deeply anesthetized and brains rapidly removed. Six sections (2 mm thick) were cut using a robent brain matrix and were stained with 2% (w/v) 2,3,5-triphenyltetrazolium chloride (TTC; Sigma, St. Louis, MO, USA). Infarct volume was analyzed with Image J software (Wayne Rasband, National Institutes of Health, USA).

Measurement of BBB permeability

BBB permeability was assessed by measuring Evans blue extravasation as previously described (Ishrat et al., 2010). Briefly, Evans blue dye (2%, 3 mL/kg; Sigma) was injected through the tail vein. 2 hours later, rats were deeply anesthetized and perfused intracardially with normal saline until colorless fl uid was obtained from the right atrium. Ipsilateral hemispheres were quickly isolated and weighed. For quantitative measurements, the ipsilateral hemispheres were homogenized in N,N-dimethylformamide and incubated for 72 hours at 37°C and then centrifuged at 21,000 ×gfor 30 minutes. Evans blue concentrations in the supernatant were determined by a microplate fl uorescence reader (Nikon, Tokyo, Japan) at excitation and emission wavelengths of 600 and 650 nm, respectively.

Expression of myeloperoxidase (MPO) in the rat brain detected by immuno fl uorescent staining

Rats were anesthetized and perfused transcardially with phosphate buffer containing 4% paraformaldehyde. Brains were post- fi xed for 24 hours, transferred into 30% sucrose solution for 24 hours, and 30 μm thick coronal brain sections were cut. Sections were incubated with rabbit anti-MPO polyclonal antibody (1：200; Sigma) overnight at 4°C. FITC-conjugated goat anti-rabbit IgG (1：400; Santa Cruz Biotechnology, Santa Cruz, CA, USA) was used as a secondary antibody. Sections were viewed under a confocal microscope (Nikon). The number of MPO+cells per mm2in ischemic brain tissue was calculated (one section with four different visual fi elds per rat).

Expression of occludin, MMP-2 and MMP-9 in the rat brain detected by western blot analysis

Brain tissue was homogenized in a commercial lysis buffer (Beyotime, Shanghai, China) containing protease inhibitors. After centrifugation, protein concentrations were determined by the Bradford assay (Bio-Rad, Hercules, CA, USA). Protein samples were separated by 10% SDSPAGE and transferred to polyvinylidene difluoride membranes. The membranes were subsequently blocked with 5% bovine serum albumin in Tris-buffered saline with Tween-20 solution and incubated with rabbit anti-occludin polyclonal antibody (1：2,000; CST, Beverly, MA, USA), rabbit anti-MMP-2 polyclonal antibody (1：1,000; Abcam, Cambridge, MA, USA), rabbit anti-MMP-9 polyclonal antibody (1：1,000; Abcam) and rabbit anti-β-actin polyclonal antibody (1:20,000; Abcam), for 12 hours at 4°C. Peroxidase-linked goat anti-rabbit IgG (1:5,000; Santa Cruz Biotechnology) and ECL reagents (Millipore, Billerica, MA, USA) were used to visualize protein bands.e absorbance of the bands was quantitated using Image J software and protein expression was normalized to the endogenous reference (β-actin) and expressed as fold difference from the sham group.

Statistical analysis

Data are expressed as mean ± SD. Statistical comparison was carried out using an independent-samplest-test with SPSS 11.5 software (SPSS, Chicago, IL, USA). One-way analysis of variance (ANOVA) with least signi fi cant difference (LSD)post hoctest was used for measurement of infarct volume. Nonparametric analysis was used for neurological deficit scores. Differences were considered statistically signi fi cant atP＜ 0.05.

Results

Effect of DHI on neurological de fi cit and infarct volume of rats after middle cerebral artery occlusion

Compared with model rats that received saline, the infarct size of rats pretreated with DHI (1.8 mL/kg) 30 minutes before middle cerebral artery occlusion showed notably smaller infarct volumes (P＜ 0.01;Figure 1A) and significantly better neurological scores (P＜ 0.01;Figure 1B).

Effect of DHI on BBB permeability and occludin expression in rats after middle cerebral artery occlusion

We speculated that DHI could result in a reduction in ischemic BBB injury. As expected, BBB permeability, assessed by Evans blue extravasation, was significantly greater in the ipsilateral hemisphere of brains from rats in the model group than in the sham group (P＜ 0.01). Administration of DHI signi fi cantly reduced Evans blue leakage and BBB permeability compared with the model group (P＜ 0.01;Figure 2A). We next examined the effect of DHI on the expression of the tight junction protein occludin in ischemic brain tissue. Occludin expression was significantly lower in the ipsilateral hemisphere of model group rats than in the sham group (Figure 2B;P＜ 0.01). The downregulation of occludin expression was markedly prevented by DHI treatment (P＜ 0.01).

Effect of DHI on neutrophil in fi ltration in rats after middle cerebral artery occlusion

MPO is a marker of neutrophil in fi ltration (Jin et al., 2011). Immunostaining showed that MPO+cells were not detected either in the contralateral hemisphere of model rats or in sham-operated rats. The number of MPO+cells in the ischemic hemisphere was notably greater in the model group than in the sham group. Neutrophil infiltration in the DHI-treated group was greater than that in the model group (Figure 3).

Effect of DHI on MMP expression in rats after middle cerebral artery occlusion

MMPs are responsible for BBB disruption by degrading the basal components of BBB and facilitating immune cell infiltration (del Zoppo et al., 2007). Western blot analy-sis showed that MMP-9 protein levels were remarkably higher in the ipsilateral hemisphere of model rats than in the sham group (P＜ 0.01). However, DHI pretreatment profoundly suppressed this upregulation (P＜ 0.01). Neither ischemia nor DHI affected the expression of MMP-2 (P＞ 0.05;Figure 4).

Effect of post-treatment with DHI on neurological de fi cit and infarct volume in rats after middle cerebral artery occlusion

Because pretreatment of DHI protected the brain against ischemic injury, we also investigated the effect of post-treatment with DHI on ischemia. We administered DHI (1.8 mL/kg) to rats 3 hours after the onset of ischemia and found that DHI could also improve neurological deficit scores and reduce infarct volume in rats after middle cerebral artery occlusion (Figure 5).

Discussion

In the present study, we explored the neuroprotective efficacy of DHI in a rat model of transient middle cerebral artery occlusion. Our results showed that pretreatment with DHI (0.9 and 1.8 mL/kg) resulted in a signi fi cantly smaller infarct volume and better neurological function than vehicle pretreatment of model rats. Administration of DHI also resulted in signi fi cantly less Evans blue leakage and neutrophil in fi ltration, as well as preventing the downregulation of occludin expression and upregulation of MMP-9 expression seen in model rats. Neither ischemia nor DHI affected the expression of MMP-2. Importantly, treatment with DHI (1.8 mL/kg) 3 hours after the onset of ischemia also prevented neurological de fi cit and reduced infarct size.

It is well documented that BBB breakdown is an important contributing factor to injury in stroke. Under ischemic stroke conditions, BBB disruption leads to increased paracellular permeability across cerebral vessels and cerebral edema (Petty and Wettstein, 2001). Blood-borne leukocytes can migrate into the brain and subsequently produce in fl ammatory factors, increase the BBB permeability and cause secondary insults (Chamorro and Hallenbeck, 2006). There is a positive correlation between myeloperoxidase-quanti fi ed neutrophil accumulation and ischemic brain injury in rats (Matsuo et al., 1994; Jin et al., 2011). Our results suggest that DHI protects the BBB from the hyperpermeability induced by middle cerebral artery occlusion and reverses the induction of neutrophil in fi ltration in ischemic tissue.

MMPs are involved in BBB opening following reperfusion injury (del Zoppo et al., 2007). Our results demonstrate that MMP-9 expression is induced in ischemic brain tissue, while MMP-2 expression is not affected by cerebral ischemia and 24 hour reperfusion. This discrepancy is explained by the difference in timescales between MMP-9 and MMP-2 expression. MMP-9 is detected in ischemic tissue within 24 hours of occlusion and is still observed at the 5 day point, while MMP-2 expression is detected predominantly after 5 days following middle cerebral artery occlusion (Romanic et al., 1998).

DHI shows good free radical scavenging capacity in the 2,2-diphenyl-1-picrylhydrazyl spectrophotometric assayin vitro(Liu et al., 2013). The beneficial effects of DHI in clinical and experimental tests have also been documented. A clinical observation suggests that DHI is conducive to the recovery of patients with traumatic intracranial hematoma (Sun et al., 2009). DHI also inhibits the maturation of dendritic cells induced by oxidatively modi fi ed low-density lipoprotein (partly by activating a PPARγ-mediated signaling pathway) (Liu et al., 2012), protects against myocardial reperfusion injury in minipigs, reduces infiltration of inflammatory cells, maintains mitochondrial integrity, and increases superoxide dismutase activity (Ma et al., 2010). In a recent study, DHI was shown to have a strong ameliorative effect on cerebral ischemia-reperfusion damage in rats because of its anticoagulant, antithrombotic, antifibrinolytic and antioxidant activities, and its regulation of Bcl-2 and Bax protein expression (He et al., 2012). Interestingly, in the present study, we report that DHI protects the BBB and reverses neutrophil infiltration. Some active components in DHI, such as salvianolic acid A and B, have a molecular weight of 700 and therefore cannot cross the blood-brain barrier. Our fi ndings elucidat the mechanism action of DHI and provide biological and molecular evidence for its clinical effects of DHI.

In summary, treatment with DHI provides protection against cerebral ischemia, mediated by a reduction in BBB permeability and reversal of neutrophil in fi ltration. Our results provide new insights into the mechanisms underlying the effects of DHI in the treatment of stroke.

Author contributions:Wang SX, Wang XM, Tan XX and Jia FF established middle cerebral artery occlusion models. Guo H and Chai LJ implemented molecular experiments. Hu LM, Zhao T and Zhao BC designed the study. All authors approved the final version of the manuscript.

Con fl icts of interest:None declared.

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Copyedited by Murphy JS, Norman C, Yu J, Yang Y, Li CH, Song LP, Zhao M

Limin Hu, Ph.D., Tianjin State Key Laboratory of Modern Chinese Medicine, Institute of Traditional Chinese Medicine Research, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China, huliminth@126.com.

10.4103/1673-5374.139462

http://www.nrronline.org/

Accepted: 2014-06-06