TIAN Dengke,HU Songyou,LING Shuang,CHEN Gangling,LI Yajuan,TANG Ning,LIU Jun,BIAN Ka,2

1.Murad Research Institute for Modernized Chinese Medicine,Shanghai University of Traditional Chinese Medicine;Shanghai 201203,China;

2.Department of Integrative Biology and Pharmacology,Institute of Molecular Medicine,University of Texas Medical School,6431 Fannin,Houston,TX 77030,USA

Hypertensive Nephropathy Treatment by Atorvastatin
——A Study of Anti-Inflammation Therapy for Target Organ Damage of Hypertension

TIAN Dengke1,HU Songyou1,LING Shuang1,CHEN Gangling1,LI Yajuan1,TANG Ning1,LIU Jun1,BIAN Ka1,2

1.Murad Research Institute for Modernized Chinese Medicine,Shanghai University of Traditional Chinese Medicine;Shanghai 201203,China;

2.Department of Integrative Biology and Pharmacology,Institute of Molecular Medicine,University of Texas Medical School,6431 Fannin,Houston,TX 77030,USA

This work was supported by grants from Key Projectof Ministry of Science and Technology(2006BAI11B08-03),E-Institutes of NitricOxide and Inflammatory Medicine of Shanghai Municipal Education Commission (E-04010)，Key Project of Shanghai Committee of Science&Technology(08430711300,08DZ1972104)

This study was designed to investigate the effect of atorvastatin(ATO)on inflammatory damage of kidney from spontaneously hypertensive rats (SHR)，and to explore preventive and therapeutic usage of ATO on hypertensive nephropathy. Male SHR of 4weeksold were divided into SHR model groupandSHR+ATO group(8 mg/kg).Age-matched Wistar-Kyoto ratswere used asnormal control.All ratswere killed at 12 wk of age.Enzyme linked immunosorbent assay(ELISA)was used to determine plasma and renal angiotensin II(AngII)contents.Renal inflammatory statuswasevaluated by the following parameters：inducible nitric oxide synthase (iNOS); intercellular adhesion molecule-1(ICAM-1);plasma and renal tissue nitrite(NO2－)concentration;histological changes of glomeruli and tubuleinterstitum of the kidney.Renal function was evaluated by urinary excretion of total protein.The results showed that ATO treatment decreasedrenal AngⅡconcentrationsignificantly.ATOinhibitedrenal inflammationasreflectedthrough reduced protein expression of iNOS and ICAM-1,decreased NO2－concentration in plasma and renal tissue.The ATO significantly improved renal function of hypertensive rats.This study indicates that ATO is a potent suppressor of renal inflammatory damage in SHR,which may serve the base for therapeutic utility of ATO in hypertensive nephropathy.

Atorvastatin;Spontaneously hypertensive rats;Inflammation;Hypertensive nephropathy

0 Introduction

Spontaneously hypertensiverats(SHR) have been widely used asa primary hypertension animal model,and multiple renal structural and functionalalterations mark the feature of hypertensive nephropathy[1～17]. Previous studies of our research center and other labs indicated that inflammatory related pathological changes have been involved in hypertensive nephropathy[2,7,11,17～19].Thus,we hypothesize that anti-inflammatory therapeutic strategy may manage hypertensive renal damage.

Atorvastatin(ATO，lipitor)is a member of the drug class known as statins,which has been effectively used for lowering blood cholesterol. Recently，ithas been reported that ATO hasprotective effect on renal injury related to hypertension.Cheng[8]indicated that without interfering with blood pressure,ATO reduced Th1 cytokine production.Little is known,however,about the mechanisms underlying the renal protective effects of ATO.

The presentstudy was designed to explore the effect of ATO on renal inflammatory damage and functional change in SHR.With thisstudy,we expect to clarify the protective mechanisms and potential clinical benefits of ATO on hypertensive renal disease.

1 Materials and Methods

1.1 Animals

Theanimal experimental procedureswerein accor dance with the Animal Use and Care guidelines of th e Experimental Animal Centerof Shanghai University of Traditional Chinese Medicine.Male SHR (4 wk of age)and WKY rats(4 wk of age)were purchased from Shang hai Experimental Animal Center of Chinese Academy of Sciences.

1.2 Materials

ATO were purchased from PfizerPharmaceuticals Limited(USA).Instrument for noninvasive blood pressure determination was purchased from Shanghai Alcott Biotech (China). Commercially available angiotensin II(Ang II)enzymelinked immunosorbent assay(ELISA)kits were obtained from BioDev Tech(China).Antibodies for rat inducible nitric oxide synthase(iNOS)and intercellular adhesion molecule-1(ICAM-1) were obtained from Santa Cruz Biotechnology Inc(USA).Computerized gel imaging analysis system was obtained from Shanghai Tannon(China).Coomassie Brilliant Blue was purchased from Sigma-Aldrich(St.Lous,MO).Multifunctional microplate reader SpectraMax 190 wasobtainedfrom Molecular Devices(USA).All chemicals were of analytical grade.

1.3 Experimental Groups and Treatment

SHR were divided into two groups：SHR model group(n=9),and SHR+ATO(n=9).ATO powder was dissolved in purified water(0.8 mg/mL),and daily administrated through intragastric gavage(8 mg/kg).Drinking water(10 ml/kg)was used for SHR model group.The treatments were carried out through the week 4 to week 12 of the age of SHR.In the whole experimental process WKY rats(n=9)were used as the age-matched control of SHR and drinking water(10 ml/kg)was used for sham treatment.

1.4 Sample Preparation

24 h urine samples were collected on the day before ratswere killed by cervical dislocation. Urine samples were lowerspeed centrifuged and supernatants were separated and stored at－20℃ until assayed for urinary concentration of total protein.

Blood samples were obtained at12 wk ofage through cardiac puncture and collected in centrifuge tubes that contained 50 μl EDTA (0.30 mol/L)，25 μl dimercaprol(0.32 mol/L),50 μl 8-hydroxyquinoline sulfate(0.34 mol/L).Plasma was separated and stored at－20℃for further assays.

Kidneys were immediately removed after scarification of the rats.One kidney was fixed with 4%paraformaldehyde for histological analysis,and another was frozen in liquid nitrogen for further protein assays.For total protein extraction,about 200 mg kidney tissueswerehomogenized in cell lysis buffer containing protein inhibitors cocktail(pH 7.4),then centrifuged for 15 min at 4℃.Concentration of total protein was determined by Lowry assay.

1.5 Plasma and Kidney AngII Determination

Ang II concentration was detected using ELISA kit according to the manufacturer's instructions.

1.6 Examination of Renal Inflammation

iNOS and ICAM-1 protein expression was analyzed by Western-blot.50 μg total protein wasseparated in sodium dodecyl sulfate polyacrylamide gel electrophoresis(SDS-PAGE)，protein was transferred to nitrocellulose membrane,and then incubated with primary antibodies of iNOS and ICAM-1(1∶200)overnight and second antibodiesconjugated with horseradish peroxidasefor 1 h.The determination was performed with enhanced chemiluminescene by exposure to Kodak X-Omat BT Films.

Griess reaction was used for the detection of renal tissue and serum NO2－concentration.100 μl of test solutions was added to 96-well flat-bottomed plates containing 100 μl/well of Griess reagent(1%sulfanilamide,0.1%naphtylethylenediamine dihydrochloride,and 5%phosphoric acid).After 10 min at room temperature the absorbance of each well was measured at 540 nm and the NO2－concentration was determined from a sodium nitrite standard curve.

1.7 Analysis of Renal Pathological Parameters

HE andPeriodicacidsilver metheramine(PASM)stained kidney sections were evaluated by using a semiquantitative histological score (score 0-3; normalto severe)for glomerulosclerosis,interstitial fibrosis,tubular atrophy,and arteriolar hyalinosis(maximal score=12)as previously described by Nakamura[13].

1.8 Evaluation of Renal Function

Urinary concentration of total protein was measured by Coomassie Brilliant Blue method.

1.9 Statistical Analysis

Data were expressed as mean±standard deviation(SD).Findings were analyzed by the SPSS11.0 software package for the one-way analysis of variance(ANOVA).The P value of less than 0.05 was considered statistically significant.

2 Results

2.1 Plasma and Kidney Ang II

In the whole experimental procedure ATO treatment failed to prevent the development of hypertension in SHR(data not shown). Plasma Ang II concentrationswere similar between WKY and SHR at 12 wk of age(P＞0.05).ATO treatment showed a tendency to increase plasma Ang II levels in the SHR group.However,these changeswere not statistically significant(P＞0.05). In contrast,kidney tissue levels of Ang II were significantly increased in SHR at12 wk ofage compared with age-matched WKY rats(P＜0.05). After8 weeksof treatment,kidney Ang II levels were markedly decreased by ATO(P＜0.05)(Table 1).

Table 1 Effect of ATO on plasma and kidney Ang II of SHR(±S)表1 ATO對SHR血漿和腎組織AngII含量的影響(±S)

Table 1 Effect of ATO on plasma and kidney Ang II of SHR(±S)表1 ATO對SHR血漿和腎組織AngII含量的影響(±S)

▲P＜0.05 vs WKY control group(SHR model group only);●P＜0.05 vs SHR model group;SHR of SHR+ATO group were daily administrated ATO (8 mg/kg) intragastrically during weeks4 through 12,SHR of SHR model group and WKY rats were daily administrated isovolumic drinking water.After plasma and renal tissue homogenateswere harvested，ELISA kit was used for the examination of AngII concentration;n=8與WKY正常對照組比較，▲P＜0.05(僅高血壓模型組)；與高血壓模型組比較，●P＜0.05；ATO治療組(8 mg/kg)每日灌胃給藥ATO 1次，高血壓模型組的SHR和WKY大鼠每日給予等量飲用水；給藥8周后收集血漿樣品和腎組織勻漿液，采用ELISA試劑盒測定AngII含量；n=8

Group Ang II Plasma(pg/mL) Kidey(pg/mg tissue)WKY control group 435.2±154.8 18.09±7.92 SHR model group 474.9±96.9 30.70±10.94▲SHR+ATO group 520.2±106.8 23.87±7.18●

2.2 Renal Protein Expression of iNOS and ICAM-1

Renal protein expression of iNOS and ICAM-1 were significantly increased in SHR at 12 wk of age compared with age-matched WKY rats(P＜0.05). Treatmentof ATO inhibited the expression ofthese inflammatory related biomarkers(P＜0.05)(Figure 1).

2.3 Plasma and Renal Tissue NO2－Concentration

Compared with WKY rats,plasma and renal tissue levels of NO2－in SHR changed in parallel with protein expression of iNOS.ATO decreased NO2－concentration in SHR after 8 weeks of treatment(P＜0.05)(Table 2).

2.4 PathologicalScores of Glomeruli and Tubuleinterstitium

Pathological scoresof glomeruli and tubule-interstitum were significantly increased in SHR at 12 wk of age compared with age-matched WKY rats(P＜0.05).After 8 weeks of treatment,ATO markedly decreased the pathological scores of glomeruli and tubule-interstitum in SHR(P＜0.05)(Figure 2).

2.5 Urinary Excretion of Total Protein

Urinary excretion oftotal protein was significantly increased in SHR at12 wk ofage compared with age-matched WKY rats (P＜0.05). ATO and HMP decreased urinary excretion of total protein after 8 weeks of treatment(P＜0.05)(Table 2).

Fig.1 Effect of ATO on iNOS and ICAM-1 protein expression in SHR kidney Total protein was extracted from kidney forWestern-blotanalysis to determine iNOS and ICAM-1 protein expressions.(A)Bands from left side corresponding to the samples from WKY,SHR,and SHR+ATO respectively.The statistics analysis of the Western blot for iNOS(B)and ICAM-1(C)were presented in bar graph.#P＜0.05 vs WKY control group(SHR model group only);*P＜0.05 vs SHR model group;n≥3圖1 ATO對SHR腎臟iNOS和ICAM-1蛋白表達的影響 提取腎臟組織總蛋白，以Western-blot法測定iNOS和ICAM-1的蛋白表達。(A)大鼠腎組織總蛋白樣品的相應(yīng)Westen-blot條帶；(B)和(C)分別為iNOS和ICAM-1的統(tǒng)計分析圖。與WKY正常對照組比較，#P＜0.05(僅高血壓模型組)；與高血壓模型組比較，*P＜0.05；n≥3

Table 2 Effect of ATO on plasma and renal tissue NO2－and urinary total protein concentration of SHR(±S)表2 ATO對SHR血漿、腎組織NO2－和尿蛋白含量的影響(±S)

Table 2 Effect of ATO on plasma and renal tissue NO2－and urinary total protein concentration of SHR(±S)表2 ATO對SHR血漿、腎組織NO2－和尿蛋白含量的影響(±S)

▲P＜0.05，▲▲P＜0.01 vs WKY control group(SHR model group only);●P＜0.05，●●P＜0.01 vs SHR model group;SHR of SHR+ATO group was daily administrated ATO(8 mg/kg)intragastrically,SHR model group and WKY ratswere daily administrated isovolumic drinking water.Griessreaction and Coomassie Brilliant Blue method were used for NO2－and urinary total protein evaluation respectively;n=9與WKY正常對照組比較，▲P＜0.05,▲▲P＜0.01(僅高血壓模型組)；與高血壓模型組比較，●P＜0.05,●●P＜0.01；ATO治療組 (8 mg/kg)每日灌胃給藥ATO 1次，高血壓模型組的SHR和WKY大鼠每日給予等量飲用水；給藥8周后處理動物，分別以Griess反應(yīng)和考馬斯亮藍法測定NO2－和尿蛋白含量；n=9

Urinary total protein(mg/day)WKY control group 15.23±4.02 0.44±0.08 7.88±1.69 SHR model group 37.59±7.82▲0.63±0.85▲▲14.91±3.18▲▲SHR+ATO group 24.10±6.27●0.43±0.11●●10.33±2.90●Group NO2－concentration Plasma(μmol/mL) Renal tissue(μmol/g)

Fig.2 Effect of ATO on pathological scores of glomeruli and tubule-interstitum in SHR Kidney samples were harvested at 12 wk of age and fixed in 4% paraformaldehyde.The pathological scores were obtained by an pathological image analysis system with HE(A～C)and PASM(D～F)stained kidney tissue sections.(A)and(D)：refer to WKY control group;(B)and(E)：refer to SHR model group;C and F：refer to SHR+ATO group;The statistics analysis of pathological scores for glomerular(G)and tuble-interstitial(H)were presented respectively.#P＜0.05,##P＜0.01 vs WKY control group(SHR model group only);*P＜0.05,**P＜0.01 vs SHR model group;n=6圖2 ATO對SHR腎小球和小管-間質(zhì)病理積分的影響 ATO給藥8周后收集腎臟組織以4%多聚甲醛固定，進行 HE(A-C)和PASM(D-F)染色后，以病理圖像分析系統(tǒng)測定病變積分。A和D：WKY正常對照組；B和E：高血壓模型組；C和F：ATO治療組；G和H分別為腎小球和小管-間質(zhì)病變積分的統(tǒng)計分析圖。與WKY正常對照組比較，##P＜0.01(僅高血壓模型組)；與高血壓模型組比較，*P＜0.05，**P＜0.01；n=6

3 Discussion

The pathological changes due to chronic inflammation are evidential in hypertensive renal disease.Interstitial fibrosis,proteinuria and decreased creatinine clearance rate manifest severe renal disorders of SHR.Our previous study indicated an increased oxidative stress and up-regulated inflammatory cytokines are presented inSHR kidney[2,17].A role of inflammatory reactionin hypertensive nephropathy is further suggested by the study of nuclear transcription factor-κB (NF-κB) inhibitor which prevented the developmentofhypertension and renal injury[10].To add more evidence,chronic treatment with p38 MAPK inhibitor delayed the onset of renal dysfunction characterized by increased total protein and albumin excretion of SHR[14].In the present study,we have evaluated the effectofATO on inflammatory related kidney damage in SHR to furtherappeal our proposed conceptthatinflammation holds the key of target organ damage of hypertension which should serve as primary target for therapeutic strategy.Our choosing of atorvastatin is due to the following considerations：1)ATO is not an anti-hypertensive drug;2)ATO exerts cardiovasculareffectthrough anti-inflammatory mechanisms;3)ATO isthe top-selling prescription medicine in the world and available immediately for therapeutic use.Our data here defines the optimal treatment of hypertension through an anti-inflammation pathway of end-organ protection.

Previous studies indicated a complex causative network involving Ang II and inflammatory cytokines in triggering renal damage in hypertension such as increasing mesangial cell proliferation,contracting afferent and efferent glomerular arteriole,and deceasing glomerular filtration rate[16]. Also，ithas been reported thatAng II stimulated the synthesis of Type I，IV collagen and fibronectin[15]，thus increasing the extracellular matrix(ECM)deposition.On theother side,olmesartan,an Ang II type-1(AT1)receptor blocker,decreased proteinuria,renal immune cells infiltration and morphology alterations in SHR by inhibition of kidney but not serum levels of Ang II[12].In thisstudy(Table 1) we observed similar result that ATO significantly inhibited kidney Ang II which imply a key role of inflammation in regulation of kidney level Ang II.

Inflammatory cytokineshavebeen crucially involved in the pathogenesis of hypertensive renal damage.Our current study(Figure 1)focused on iNOS and ICAM and showed that ATO decreased expression of the inflammatory molecules.The production of unphysiological higher concentration of nitricoxide (NO) by iNOS hasbeen considered as a pro-inflammatory mediator and implicated in several inflammatory diseases[3～6]. Inflammatory cytokines,including interleukin-1β (IL-1β),tumor necrosis factor-α (TNF-α)，interferon-γ (IFN-γ) and bacterial lipopolysaccharide (LPS) can induce the expression of iNOS in monocyte/macrophages,neutrophil granulocytes and many other cell types.The over-produced NO will react with superoxide anion(O2·－)to form peroxynitrite(ONOO－),which can react with tyrosine residue to form nitrotyrosin and cause tissue injury including renal damage[3～6]. In current study plasma and renal tissue NO2－concentration was evaluated as the consequence of over expressed iNOS which could be inhibited by ATO treatment(Table 2).Up-regulation of ICAM-1 in tubular epithelial cells was observed in kidney diseases with inflammatory reaction[17,18]which actively participate progress of fibrosis in glomeruli and tubule-interstitum[1,9].Our study(Figure 1)indicated that the ICAM-1 expression was significantly inhibited by ATO treatmentand suggests an action mechanism of ATO in preserving renal function and reducing interstitial fibrosis.

Hypertensive nephropathy marks with increased urinary excretion of total protein,which ismostly attributed to increased permeability of glomerularfiltration membrane，damage ofelectrostatic barrierand renal tubular reabsorption. Our current and previous studies have detected that renal pathological changes in SHR at 12 wk of age including：1)accumulation of mesangial matrix,thickening and focal sclerosis of capillary basement membrane;2)cloudy swelling and irregular basement membrane thickening of renal tubules;3)interstitial inflammatory cell infiltration,accumulation of ECM and fibrosis;4)increased concentration of urinary β2-microglobulin concentration (β2-MG). In the presentstudy,ATO effectively reversed pathological scores of glomeruli and tubule-interstitum in SHR and strongly demonstrated the efficacy of anti-inflammation therapy on hypertensive renal injury(Figure 2).The restoration of normal renal function(measured by urinary protein excretion)by ATO further prove our concept of anti-inflammation therapy for hypertensive target organ damage.

4 Conclusions

In conclusion，this study demonstrates thatATO inhibited inflammatory statusof the hypertensive kidney which was associated with a marked restoration of kidney function in SHR.It isworth to noting that the protective effect of ATO on hypertensive renal diseases is not related to the change of plasma AngII but renal tissue AngII concentration.We propose that anti-inflammation mechanism may servethebasefor therapeutic usage of ATO in hypertensive nephropathy.

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阿托伐他汀對高血壓腎臟并發(fā)癥炎性損傷的治療作用

田登科1，胡送友1，凌 霜1，陳剛領(lǐng)1，李亞娟1,唐 寧1，劉 俊1，卞 卡1,2
1.上海中醫(yī)藥大學(xué)穆拉德中藥現(xiàn)代化研究中心，上海 201203；
2.美國德克薩斯大學(xué)休斯頓醫(yī)學(xué)院綜合生物及藥理學(xué)系，德克薩斯大學(xué)分子醫(yī)學(xué)研究所，休斯頓 TX 77030

2010-03-10；接受日期：2010-03-31

國家科技部“十一·五”支撐計劃 (2006BAI11B08-03)；上海市教委高校一氧化氮與炎癥醫(yī)學(xué)E-研究院計劃(E-04010)；上海市科委基礎(chǔ)研究重點項目(08430711300，08DZ1972104)

卞卡，電話：(021)51322535，傳真：(021)51322446，E-mail：Ka.Bian@uth.tmc.edu

通過考察阿托伐他汀（atorvastatin，ATO）對自發(fā)性高血壓大鼠（spontaneously hypertensive rats，SHR）腎臟炎性損害的影響，探討了ATO對高血壓腎臟并發(fā)癥的防治作用。將4周齡SHR分為高血壓模型組和ATO治療組（8 mg/kg），以同周齡的Wistar-Kyoto大鼠為正常對照。灌胃給藥8周后，采用酶聯(lián)免疫法（enzyme linked immunosorbent assay）測定血漿和腎組織血管緊張素Ⅱ（angiotensin，AngⅡ）含量；測定誘導(dǎo)性一氧化氮合酶（inducible nitric oxide synthase，iNOS）及細胞間粘附分子 -1（intercellular adhesion molecule-1，ICAM-1）的蛋白表達和亞硝酸陰離子（nitrite，NO2－）含量，以評價腎臟炎癥狀態(tài)；以蘇木素伊紅（hematoxylin and eosin）和過碘酸六胺銀染色（periodic acid-silver metheramine）染色示SHR腎小球和腎間質(zhì)形態(tài)學(xué)病變，并以尿蛋白含量為指標衡量腎臟功能。結(jié)果顯示，ATO給藥后顯著降低了SHR腎組織AngⅡ含量；腎組織iNOS和ICAM-1的蛋白表達及NO2－含量明顯降低，同時伴隨著SHR腎臟病理形態(tài)的改善和腎功能的提高。該研究表明，ATO可顯著改善SHR腎臟炎性損害，ATO可能在高血壓腎臟并發(fā)癥的防治方面有一定的療效。

阿托伐他?。蛔园l(fā)性高血壓大鼠；炎癥；高血壓腎病

R544.1；R285.5

Mar 10,2010 Accepted：Mar 31,2010

BIAN Ka,Tel：+86(21)51322535,Fax：+86(21)51322446,

E-mail：Ka.Bian@uth.tmc.edu