Home | Register | Login | Inquiries | Alerts | Sitemap |  


Advanced Search
JKM > Volume 37(2); 2016 > Article
Jung and Shin: The Effects of Lycii Radicis Cortex on Inflammatory Response through an Oxidative Stress and AGEs-mediated Pathway in STZ-induced Diabetic Rats

Abstract

Objectives

This study examined whether Lycii Radicis Cortex has an inhibitory effect on inflammatory response through an oxidative stress and advanced glycation endproducts (AGEs)-mediated pathway in streptozotocin (STZ)-induced type 1 diabetic rats.

Methods

Lycii Radicis Cortex was orally administered to STZ-induced diabetic rats in doses of 80 or 160 mg/kg body weight/day for 2 weeks, and its effects were compared with those of diabetic control and normal rats.

Results

The administration of Lycii Radicis Cortex decreased the elevated serum urea nitrogen and renal reactive oxygen species (ROS), and reduced the increased AGEs in the serum and kidney. The elevated protein expressions of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase subunits in the kidney of diabetic control rats were significantly decreased after Lycii Radicis Cortex treatments. Moreover, the kidney of diabetic rats exhibited the up-regulation of receptor for AGEs (RAGE) and AGEs-related proteins; however, Lycii Radicis Cortex treatment also significantly reduced those expressions (excepted RAGE). In addition, the diabetic rats exhibited an up-regulation of the expression of proteins related to inflammation in the kidney, but Lycii Radicis Cortex administration reduced significantly the expression of the inflammatory proteins through the nuclear factor-kappa B (NF-κB) and activator protein-1 (AP-1) pathways.

Conclusions

This study provides scientific evidence that Lycii Radicis Cortex exerts the antidiabetic effect by inhibiting the expressions of AGEs and NF-κB in the STZ-induced diabetic rats.

Introduction

Diabetes mellitus is a metabolic disease characterized by prolonged hyperglycemia that can lead to micro and macrovascular diseases. Especially the microvascular injury in diabetes mainly targets three major organs, the eye, peripheral nerve, and kidney1,2). Diabetic nephropathy is the most common cause of end-stage renal disease, and could account for disability and high mortality rate in patients with diabetes. The pathogenesis of diabetic nephropathy is multifactorial in which long-term hyperglycemia plays a crucial role2). During diabetic milieu, supraphysiological glucose is involved in the formations of advanced glycation endproducts (AGEs) and the mitochondrial productions of free radicals, and leading consequently to cell death and renal dysfunction. Therefore, oxidative stress plays a pivotal role for the development of diabetic nephropathy, which is characterized by the thickening of glomerular basement membranes, expansion of mesangial cells, glomerular hypertrophy, loss of podocytes, expansion of tubular basement membranes, tubular atrophy, interstitial fibrosis, and arteriosclerosis3).
AGEs and nonenzymatic glycation of proteins contribute to diabetic tissue injury. The accumulation of AGEs in kidney and other tissues of patients with diabetes mellitus has been implicated in the development of diabetic nephropathy and vasculopathy4,5). AGEs may contribute to diabetic tissue injury by at least two major mechanisms. The first is receptor -independent alteration of the extracellular matrix architecture by nonenzymatic glycation and the formation of protein crosslinks. The second mechanism is receptor-dependent and consists of modulation of cellular functions through ligation of specific cell surface receptors, the best characterized of which is the receptor for AGEs (RAGE)6,7). AGEs-RAGE binding, which activates nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase, is a central player in the production of superoxide radicals8). AGEs have been shown to induce oxidative stress and to activate two major pro-inflammatory transcription factors such as nuclear factor-kappa B (NF-κB) and activator protein-1 (AP-1)9).
The root bark of Lycium chinense Miller, Lycii Radicis Cortex, extract has been widely used as a traditional Korean medicinal herb for centuries. Lycii Radicis Cortex is sweet in taste and cold in nature and effectively works for the kidney, lung and liver channels. The medicinal plant has been extensively applied for diabetes mellitus with the traditional functions of cooling the blood, bringing down hectic fever, clearing away heat, and removing fire in the lung10). Pharmacological studies in animal models or cell lines revealed that extracts from Lycii Radicis Cortex are able to lower blood pressure11), serum glucose12), lipid levels13), and to improve insulin resistance14). Our previous study has shown that the Lycii Radicis Cortex extract reduces oxidative stress and its related renal damage in cisplatin-induced nephrotoxicity rats15). In addition, it has been proved that the major compound of Lycii Radicis Cortex is plenty of phenols, which have favorable effects of protection against inflammation, atherosclerosis, cancer, and diabetes in association with oxidative stress 1619). Therefore, in this study, we examined the effect of Lycii Radicis Cortex on the oxidative stress- and reactive oxygen species (ROS)-related factors involved in the development of diabetic damage using streptozotocin (STZ)-induced type 1 diabetic rats.

Materials and Methods

1. Materials

The protease inhibitor mixture, ethylenediaminetetraacetic acid (EDTA) were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan). 2′,7′-Dichlorofluorescein diacetate (DCFH-DA) was obtained from Molecular Probes (Eugene, OR, USA). The Bio-Rad protein assay kit and pure nitrocellulose membrane were supplied by Bio-Rad Laboratories (Seoul, Korea). Phenylmethylsulfonyl fluoride (PMSF) was acquired from Sigma Chemical Co. (St. Louis, MO, USA). Rabbit polyclonal antibodies against RAGE, NAD(P)H oxidase-4 (Nox-4), p22 phagocytic oxidase (p22phox), p47phox, NF-κBp65, and mouse monoclonal antibodies against cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS), β-actin, histone and goat polyclonal antibodies against tumor necrosis factor-a (TNF-a) and inteleukin-1β (IL-1β) were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). Rabbit polyclonal anti-AP-1 gene c-FOS were obtained from Cell Signaling Technology, Inc. (Cell Signaling, MA, USA). Monochlonalanti-Ne-(carboxyethyl) lysine (CEL) antibody, and polyclonal anti-Ne-(carboxymethyl) lysine (CML) antibody were kindly provided by Dr. R. Nagai (Kumamoto University, Japan). Goat anti-rabbit and goat anti-mouse immunoglobulin G (IgG) horseradish peroxidase (HRP)-conjugated secondary antibodies were acquired from Santa Cruz Biotechnology, Inc. ECL Western Blotting Detection Reagents were supplied by GE Healthcare (Piscataway, NJ, USA).

2. Preparation of Lycii Radicis Cortex Extracts

Lycii Radicis Cortex, collected in China, was purchased from Human-herb (Gyeongsan, Korea). To prepare the Lycii Radicis Cortex extract, the roots (150 g) of Lycii Radicis Cortex were boiled gently in 2 L of water for 3 h. After filtration, the solution was evaporated under reduced pressure and then freeze dried to provide an extract with a yield of 10% by weight of the starting materials. A voucher specimen of Lycii Radicis Cortex has been deposited at the herbarium located at the College of Korean Medicine, Daegu Haany University.

3. Experimental Animals and Treatment

Animal experiments were performed according to the “Guidelines for Animal Experimentation” approved by Daegu Haany University. Six-week-old male Sprague-Dawley rats were purchased from Daehan-Bio (Chungcheong, Korea). The rats were maintained under a 12-h light/dark cycle, and housed in a controlled temperature (22 ± 2°C) and humidity (40 ± 5%) environment. After several days of adaptation, the rats were randomly separated into normal control (n=6) and diabetic groups. The diabetic groups were injected intraperitoneally with STZ (Sigma-Aldrich, St. Louis, MO, USA) (50 mg/kg body weight) in 10 mM citrate buffer (pH 4.5). After 3 days of STZ injection, the glucose levels of blood taken from the tail veins were measured, and then the STZ-induced diabetic rats were divided into three groups. Treatment with Lycii Radicis Cortex was initiated after confirming the induction of hyperglycemia in the diabetic rats by weight (197.3 ± 0.2 g) and serum glucose (399.0 ± 0.5 mg/dl). The diabetic control group (n=6) was given water orally, while the other two groups (n=6 per group) were orally administered with Lycii Radicis Cortex extracts daily for 14 days at a dose of 80 or 160 mg/kg body weight, respectively. The non-diabetic rats (n=6) as the normal group were compared with the diabetic groups. Body weight, food intake and water intake were determined every day during the experimental period. After administration for 14 days, blood samples were collected from the abdominal aorta of anaesthetized rats. Serum was separated immediately by centrifugation. Subsequently, each rat was perfused with ice-cold physiological saline, and then the kidney was harvested, snap-frozen in liquid nitrogen and stored at −80°C until analysis were performed.

4. Analysis of the Serum Parameters

The serum glucose was measured using a commercial kit (Glucose CII-Test from Wako Pure Chemical Industries, Ltd., Osaka, Japan). The renal functional parameter (serum urea nitrogen) was measured using a commercial kit (BUN Kainos from Kainos Laboratory Inc., Tokyo, Japan). The serum ROS level was determined using the method reported by Ali et al20). Serum glycosylated protein was colorimetrically measured by determining 5-hydroxymethyl furfural formation from glucose according to the thiobarbituric acid assay21).

5. Measurement of Renal Glucose and AGEs Levels

The renal glucose level was determined by the method of Momose et al.22), with some modifications. Renal tissues were homogenized with ice-cold 0.9% NaCl buffer, and then the homogenate was deproteinized by centrifugation at 1,670 × g for 15 min at 4°C, and then the glucose level was determined using the Wako kit after incubation for 30 min at 37°C. The renal AGEs level was determined by the method of Nakayama et al.23). Minced kidney tissue was delipidated with chloroform and methanol (2:1, v/v) overnight. After washing with methanol and distilled water, the tissue was homogenized in 0.1 N NaOH, followed by centrifugation at 8,000 × g for 15 min at 4°C. The amounts of AGEs in these alkali-soluble samples were determined by measuring the fluorescence at an emission wavelength of 440 nm and an excitation wavelength of 370 nm. A native bovine serum albumin (BSA) preparation (1 mg/ml of 0.1 N NaOH) was used as a standard and the fluorescence intensity values of the samples were measured at a protein concentration of 1 mg/ml and expressed in arbitrary units (AU) compared with the native BSA preparation.

6. Measurement of Renal ROS Generation Level

ROS generation was measured using the method reported by Ali et al.20) Renal tissues were homogenized on ice with 1 mM EDTA-50 mM sodium phosphate buffer (pH 7.4), and 25 mM DCFH-DA was then added to the homogenates. After incubation for 30 min, the changes in fluorescence were determined at an excitation and emission wavelength of 486 nm and 530 nm, respectively.

7. Preparation of Nuclear and Post-Nuclear Fractions

Nuclear protein extraction was performed using the method reported by Komatsu24). Briefly, renal tissues were homogenized with ice-cold lysis buffer containing 5 mM Tris-HCl (pH 7.5), 2 mM MgCl2, 15 mM CaCl2 and 1.5 M sucrose, followed by the addition of a 0.1 M dithiothreitol (DTT) and a protease inhibitor mixture. After centrifugation (10,500 × g for 20 min at 4°C), the pellet was suspended with an extraction buffer containing 20 mM 2-[4-(2-hydroxyethyl)-1-piperazyl] ethanesulfonic acid (pH 7.9), 1.5 mM MgCl2, 0.42 M NaCl, 0.2 mM EDTA and 25% (v/v) glycerol, followed by the addition of a 0.1 M DTT and protease inhibitor mixture. The mixture was placed on ice for 30 min. The nuclear fraction was prepared by centrifugation at 20,500 × g for 5 min at 4°C.
The post-nuclear fraction was extracted from the kidneys of each rat. Briefly, the renal tissue was homogenized with ice-cold lysis buffer (pH 7.4) containing 137 mM NaCl, 20 mM Tris–HCl, 1% Tween 20, 10% glycerol, 1 mM PMSF, and a protease inhibitor mixture. The homogenate was then centrifuged at 2,000 × g for 10 min at 4°C. The protein concentration in each fraction was determined using a Bio-Rad protein kit (Bio-Rad Laboratories, Hercules, CA, USA).

8. Western blot Analyses

To determine NF-κBp65, AP-1, and histone, 10 mg of protein from each nuclear fraction underwent 8% sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE). The separated proteins were transferred to a nitrocellulose membrane, blocked with a 5% (w/v) skim milk solution for 1 h, and incubated separately with the primary antibodies to NF-κBp65, AP-1, and histone overnight at 4°C. After washing the blots, they were incubated with the anti-rabbit or anti-mouse IgG HRP-conjugated secondary antibody for 1 h at room temperature. In addition, 10 mg of protein of each post-nuclear fraction of RAGE, CML, CEL, Nox-4, p22phox, p47phox, COX-2, iNOS, IL-1β, TNF-a, and β-actin was electrophoresed through 8–15% SDS-PAGE. Each antigen-antibody complex was visualized using ECL Western Blotting Detection Reagents and detected by chemiluminescence with SENSI-Q2000 Chemodic (Lugen Sci. co., Ltd, Seoul, Korea). The band densities were determined using ATTO Densitograph Software (ATTO Corporation, Tokyo, Japan), and quantified as a ratio to β-actin or histone. The protein levels of the groups are expressed relative to those of the normal rats (represented as 1).

9. Statistical Analysis

Data were expressed as the mean ± SD. Statistical comparisons were performed using one-way analysis of the variance (ANOVA) followed by a Dunnett’s test (SPSS 11.5.1 for Windows, 2002; SPSS Inc., Chicago, IL, USA). The p values < 0.05 were considered significant.

Results

1. Body weight, kidney weight, food intake, and water intake

Table 1 shows the changes in body weight, kidney weight, food intake, and water intake during the experimental period. The diabetic control rats showed a significant decrease in body weight gain. On the other hand, the kidney weight and the food and water intakes in diabetic control rats were markedly higher than those of in normal rats. Compared to the diabetic control rats, the administration of Lycii Radicis Cortex significantly decreased the water intake at both the 80 and 160 mg/kg body weight/day, but the body and kidney weight and food intake were not changed throughout the experimental period.

2. Biochemical analysis

As shown in Table 2, the serum and kidney glucose levels were significantly increased in diabetic control rats. Lycii Radicis Cortex administration significantly reduced the glucose levels at both the 80 and 160 mg/kg body weight/day in kidney, but it led to a tendency towards a slight decrease without significance in serum. The oxidative stress-related biomarker, the ROS, in the serum and kidney of diabetic control rats was higher than those in the normal rats. The administration of Lycii Radicis Cortex decreased the serum ROS level, but there was no statistical significance. However, in contrast in kidney, the Lycii Radicis Cortex treatment significantly decreased the ROS level in diabetic rats. In addition, the serum and kidney levels of AGEs in diabetic control rats were significantly higher than normal rats. However, Lycii Radicis Cortex treatment showed significant reduction in a dose-dependent manner in both serum and kidney. Urea nitrogen, a renal functional parameter, was markedly increased in diabetic control rats compared to normal rats, but it was significantly attenuated by the administration of Lycii Radicis Cortex at a dose of 160 mg/kg body weight/day.

3. Renal NADPH-oxidase protein expressions

The expression level of the p47phox protein is significantly elevated in the kidney of the diabetic control rats compared to the normal rats (Fig. 1C). However, the levels of NOX-4 and p22phox expressions were not changed significantly in the diabetic control rats (Fig. 1A and 1B). On the other hand, the administration of Lycii Radicis Cortex significantly reduced NOX-4, p22phox, and p47phox protein expressions at a dose of 160 mg/kg body weight/day.

4. AGEs-related protein expressions in the kidney

Since the administration of Lycii Radicis Cortex reduced glucose levels in the kidney, we further investigated the expression of AGEs-related proteins such as RAGE, CEL, and CML by employing Western blot analysis. As shown in Fig. 2, renal RAGE, CEL, and CML were significantly elevated in diabetic control rats. Lycii Radicis Cortex-treated rats showed a significant down-regulation of CEL and CML in a dose-dependent manner (Fig. 2B and 2C). The expression levels of RAGE were reduced slightly by Lycii Radicis Cortex without significance (Fig. 2A).

Discussion

Recently, traditional oriental herbal medicines have been the subject of focus due to their beneficial effects observed during clinical experience accumulated over a long time and their absence of toxic or side-effects. There have thus been many studies to identify effective therapeutic agents from traditional medicines for diabetes and complications. Therefore, in this study, we investigated the effect of Lycii Radicis Cortex on the oxidative stress and ROS related factors involved in the development of diabetic renal damage using STZ-induced type 1 diabetic rats.
Insulin resistance or insulin secretion deficiency in diabetes mellitus leads to physic-metabolic abnormalities such as a decline in body weight gain and increases in food intake, water intake, urine volume, and kidney weight25). In this study, our diabetic models showed same conditions. The administration of Lycii Radicis Cortex for 14 days led to no significant difference in body and kidney weight and food intake; however, water intake was significantly reduced by both the 80 and 160 mg/kg administrations (Table 1). These results suggest that the oral administration of Lycii Radicis Cortex may improve the typical diabetic symptom, an excessive intake of water.
We observed a significant elevation of serum and renal glucose levels in diabetic rats compared with non-diabetic rats. The serum glucose levels of Lycii Radicis Cortex-treated rats was slightly lower than those of diabetic control rats; however, the concentration of renal glucose was significantly reduced by both the 80 and 160 mg/kg administrations (Table 2). It seems these results are related to that Lycii Radicis Cortex has been used as a traditional Korean herbal remedy for kidney for centuries26). Furthermore, renal functional parameters, such as urea nitrogen levels, were increased in the serum of the diabetic control group; however, urea nitrogen was significantly lowered by Lycii Radicis Cortex treatment (Table 2). These results show that Lycii Radicis Cortex treatment may ameliorate diabetic pathological conditions induced by hyperglycaemia, and may lead to improvement in the impaired renal function of diabetic rats.
Hyperglycemia is a major cause for the enhanced generation of ROS, leading to increased oxidative stress in an impaired antioxidant defense state27). ROS are considered to play a direct, central role in the pathophysiological mechanisms underlying development of various diabetic complications, because they directly oxidize and damage various tissue biomolecules, such as DNA, protein, and lipids, consequently resulting in cell dysfunction and apoptosis28,29). In the present study, diabetic rats exhibited a significant increase in levels of serum and renal ROS. On the other hand, Lycii Radicis Cortex treatment significantly reduced renal ROS in a dose-dependent manner, and showed a tendency for decrease without significance in serum (Table 2). NADPH oxidase, a major source of ROS, has been reported to be increased in experimental models of diabetic nephropathy, and importantly, the inhibition of NADPH oxidase leads to a reduction in the renal ROS production and amelioration in the morphological changes and functional abnormalities that are seen under hyperglycemia30). In addition, NADPH oxidase has been suggested to mediate generation of ROS during AGEs and RAGE interactions31). In our experiment, the diabetic control rats showed a significant up-regulated expression level of p47phox, a subunit of NADPH oxidase, compared to that in the normal rats. However, Lycii Radicis Cortex significantly reduced the p47phox level in the 160 mg/kg-treated rats (Fig. 1C). NOX-4 and p22phox were slightly increased in diabetic control rats without significance, but Lycii Radicis Cortex-treated rats showed a significant reduction of those expression levels in the 160 mg/kg-administered rats (Fig. 1A and 1B). Consequently, these results demonstrated that Lycii Radicis Cortex effectively attenuated oxidative stress, at least in part, through the direct inhibition of ROS and NADPH oxidase.
The elevated levels of glucose starts forming covalent adducts with plasma proteins through a non-enzymatic process known as glycation, and in the last stage, stable glycation products, AGEs, are formed32). AGEs are removed and metabolized by the kidney, but the kidney is also a site for the accumulation of AGEs and AGEs-associated damage33). AGEs provoke the synthesis of fibronectin, laminin, and typeIV collagen in the kidney, promoting glomerular sclerosis, interstitial fibrosis, and hypertrophy34). Additionally, the interaction of AGEs with the RAGE triggers ROS generation, NADPH oxidase and adhesion molecules expressions, and upregulates inflammation through NF-κB and other signaling pathways35,36). Therefore, the accumulation of AGEs in the kidney has been regarded as an indicator of progressive renal damage in diabetic complications. Actually, in the present study, the vehicle-treated diabetic rats showed significantly elevated levels of AGEs in serum and kidney and also, over-expressions of renal RAGE. However, the administration of Lycii Radicis Cortex significantly reduced the increased formation of AGEs in both serum and kidney (Table 2). There was only a tendency towards a decrease in the RAGE expression level from the treatment with Lycii Radicis Cortex (Fig. 2A).
One of the major AGEs, CML is generated through several pathways, such as oxidative cleavage of Amadori product by the hydroxyl radical, peroxynitrite, and also glyoxal which is generated via autoxidation of glucose3739). Since CML formation requires oxidation in all pathways, CML is considered to be the important biomarker of oxidative stress40). In addition, CEL is reported to be generated during the reaction of methylglyoxal with lysine residues and is detected in human lens proteins at a concentration similar to that of CML. Accumulation of those AGEs increases with age and diabetes mellitus1,41). In the present study, the diabetic control rats showed enhanced protein expressions of renal CML and CEL. However, the administration of Lycii Radicis Cortex significantly down-regulated renal CEL and CML protein expression levels in a dose-dependent manner (Fig. 2B and 2C). These results suggest that Lycii Radicis Cortex can prevent diabetic renal damage through inhibiting AGEs formation, rather than AGEs-RAGE binding.
The pathobiological processes modulated by hyperglycemia and oxidative stress include inflammatory responses42). NF-κB plays a central role in oxidative stress-induced inflammatory responses by the regulation of transcription and the expression of a large number of genes, including growth factors, pro-inflammatory cytokines and others43). In particular, the activation of NF-κ B induces the inflammatory enzymes, such as COX-2 and iNOS, and subsequent production of prostaglandin E2 and nitric oxide, respectively44). AP-1, a heterodimer complex, which is typically composed of c-FOS and c-Jun, is another major redox-sensitive transcriptional factor that may be relevant to the biology of diabetic nephropathy45,46). In this study, elevated activations of NF-κB and AP-1 in the kidneys of the diabetic control rats were significantly down-regulated by Lycii Radicis Cortex administration in a dose-dependent manner (Fig. 3A and 3B). In addition, the administration of Lycii Radicis Cortex significantly decreased the protein expression level of renal COX-2 in the 160 mg/kg-treated rats, compared to that in diabetic control rats (Fig. 4A). Concerning iNOS, there was no significant difference between normal and diabetic control rats, although, Lycii Radicis Cortex treatment showed a significant decrease at a dose of 160 mg/kg body weight/day (Fig. 4B). Renal TNF-a and IL-1β expression levels were significantly increased in diabetic control rats, compared to those in the normal rats. However, the administration of Lycii Radicis Cortex significantly attenuated the level of renal IL-1β expressions in the 160 mg/kg-treated rats (Fig. 4D). Regarding the protein expressions level of TNF-a, Lycii Radicis Cortex treatment showed a reduced tendency, but it was not significant (Fig. 4C). On the basis of these results, we suggested that Lycii Radicis Cortex can adjust inflammation by inhibiting the NF-κB or AP-1 pathway in the diabetic kidney.

Discussion

In conclusion, STZ-induced diabetic rats showed increased renal damage associated with the hyperglycemia-mediated oxidative stress and AGEs formation-derived pro-inflammatory transcription factors (NF-κB and AP-1), and pro-inflammatory genes (COX-2, iNOS, TNF-a, IL-1β). On the other hand, these unfavorable outcomes were reversed by Lycii Radicis Cortex administration in the kidney of diabetic rats. Lycii Radicis Cortex treatment of diabetic rats improved the overall renal function, that is confirmed through serum urea nitrogen level. Therefore, the present study suggests that Lycii Radicis Cortex is expected to provide a novel therapeutic strategy for the development of diabetic complications and further biological investigation is needed.

Fig. 1
Renal NADPH oxidase subunits protein expressions
Representative immunoblots for (A) NOX-4, (B) p22phox, and (C) p47phox. Immunoblotting analysis was performed as described in Materials and methods. N: normal rats, Veh: vehicle-treated diabetic rats, L80: Lycii Radicis Cortex 80 mg/kg body weight-treated diabetic rats, L160: Lycii Radicis Cortex 160 mg/kg body weight -treated diabetic rats. Data are the mean±SD. Significance: *p<0.05, **p<0.01, ***p<0.001 versus vehicle-treated diabetic rats.
jkm-37-2-62f1.gif
Fig. 2
Renal receptor for advanced glycation endproducts, CEL, and CML protein expressions.
Representative immunoblots for (A) RAGE, (B) CEL, and (C) CML. Immunoblotting analysis was performed as described in Materials and methods. N: normal rats, Veh: vehicle-treated diabetic rats, L80: Lycii Radicis Cortex 80 mg/kg body weight-treated diabetic rats, L160: Lycii Radicis Cortex 160 mg/kg body weight-treated diabetic rats. Data are the mean±SD. Significance: *p<0.05, **p< 0.01, ***p<0.001 versus vehicle-treated diabetic rats.
jkm-37-2-62f2.gif
Fig. 3
Levels of renal NF-κBp65 and c-FOS activity.
Representative immunoblots for (A) NF-κBp65 and (B) AP-1. Immunoblotting analysis was performed as described in Materials and methods. N: normal rats, Veh: vehicle-treated diabetic rats, L80: Lycii Radicis Cortex 80 mg/kg body weight-treated diabetic rats, L160: Lycii Radicis Cortex 160 mg/kg body weight-treated diabetic rats. Data are the mean±SD. Significance: *p<0.05, **p<0.01 versus vehicle-treated diabetic rats.
jkm-37-2-62f3.gif
Fig. 4
Renal inflammation-related protein expressions.
Representative immunoblots for (A) COX-2, (B) iNOS, (C) TNF-a, and (D) IL-1β. Immunoblotting analysis was performed as described in Materials and methods. N: normal rats, Veh: vehicle-treated diabetic rats, L80: Lycii Radicis Cortex 80 mg/kg body weight-treated diabetic rats, L160: Lycii Radicis Cortex 160 mg/kg body weight-treated diabetic rats. Data are the mean±SD. Significance: *p<0.05, **p<0.01 versus vehicle-treated diabetic rats.
jkm-37-2-62f4.gif
Scheme 1
Possible mechanism of Lycii Radicis Cortex in the kidney of diabetic rats.
jkm-37-2-62scheme1.gif
Table 1
Body Weight, Kidney Weight, Food Intake, and Water Intake
Group Body weight gain (g/16 days) Kidney weight (g/body weight) Food intake (g/day) Water intake (ml/day)
N 77.5 ± 7.0b 0.77 ± 0.02c 19.73 ± 0.1c 66.8 ± 3.3c
Veh 49.3 ± 3.1 1.19 ± 0.06 29.43 ± 0.1 122.6 ± 5.0
L80 48.3 ± 7.4 1.14 ± 0.04 29.43 ± 0.2 106.4 ± 4.9a
L160 51.0 ± 7.0 1.13 ± 0.02 29.6 ± 0.1 103.8 ± 6.3a

N: normal rats, Veh: vehicle-treated diabetic rats, L80: Lycii Radicis Cortex 80 mg/kg body weight-treated diabetic rats, L160: Lycii Radicis Cortex 160 mg/kg body weight-treated diabetic rats. Data are the means ± SD.

Significance:

a p<0.05,

b p<0.01,

c p<0.001 versus vehicle-treated diabetic rats.

Table 2
Biochemical Analysis
Item Normal rats Diabetic rats
Veh L80 L160
Serum
Glucose (mg/dl) 133 ± 5c 466 ± 56 416 ± 25 404 ± 15
ROS (fluorescence/min/ml) 61.5 ± 9.6b 81.6 ± 1.5 80.7 ± 12.0 66.8 ± 7.0
Glycosylated protein (nmol/mg protein) 1.03 ± 0.05c 1.76 ± 0.14 1.25 ± 0.09a 1.24 ± 0.08b
Urea-N (mg/dl) 30.0 ± 1.3a 51.7 ± 8.1 42.3 ± 3.3 34.9 ± 1.2a
Kidney
Glucose (mg/mg protein) 0.22 ± 0.03b 0.48 ± 0.07 0.32 ± 0.01a 0.33 ± 0.02a
ROS (fluorescence/min/mg protein) 15.0 ± 0.6b 21.5 ± 1.2 16.8 ± 0.9a 15.1 ± 0.7b
AGE (AU) 1.00 ± 0.10c 1.76 ± 0.09 0.96 ± 0.08a 0.86 ± 0.11a

ItemNormal rats

Veh: vehicle-treated diabetic rats, L80: Lycii Radicis Cortex 80 mg/kg body weight-treated diabetic rats, L160: Lycii Radicis Cortex 160 mg/kg body weight-treated diabetic rats. Data are the means±SD.

Significance:

a p<0.05,

b p<0.01,

c p<0.001 versus vehicle-treated diabetic rats.

References

1. Peppa M, Vlassara H. Advanced glycation endproducts and diabetic complications: A general overview. Hormones. 2005; 4:28–37.
crossref

2. Kikkawa R, Koya D, Haneda M. Progression of diabetic nephropathy. Am J Kidney Dis. 2013; 41:S19–21.
crossref

3. Forbes JM, Coughlan MT, Cooper ME. Oxidative stress as a major culprit in kidney disease in diabetes. Diabetes. 2008; 57:1446–54.
crossref

4. Ruderman N, Wiliamson J, Brownlee M. Glucose and diabetic vascular disease. FASEB J. 1992; 6:2905–14.


5. Schmidt AM, Yan SD, Stern DM. The dark side of glucose. Nature. 1995; Med1:1002–4.
crossref

6. Neeper M, Schmidt AM, Brett J, Yan SD, Wang F, Pan YC, et al. Cloning and expression of a cell surface receptor for advanced glycosylation endproducts of proteins. J Biol Chem. 1992; 267:14998–15004.


7. Schmidt AM, Vianna M, Gerlach M, Brett J, Ryan J, Kao J, et al. Isolation and characterization of two binding proteins for advanced glycosylation endproducts from bovine lung which are present on the endothelial cell surface. J Biol Chem. 1992; 267:14987–97.


8. Wautier MP, Chappey O, Corda S, Stern DM, Schmidt AM, Wautier JL. Activation of NADPH oxidase by AGE links oxidant stress to altered gene expression via RAGE. Am J Physiol Endocrinol Metab. 2001; 280:E685–94.


9. Simm A, Münch G, Seif F, Schenk O, Heidland A, Richter H, et al. Advanced glycation endproducts stimulate the MAP-kinase pathway in tubulus cell line LLC-PK1. FEBS Lett. 1997; 410:481–4.
crossref

10. Wang FY, Luo JY. Dictionary of Traditional Chinese Materia Medica. Hunan: Hunan Science and Technology Press;2006. p. 167


11. Funayama S, Yoshida K, Konno C, Hikino H. Structure of kukoamine A, a hypotensive principle of Lycium chinense root barks 1. Tetrahedron Lett. 1980; 21:1355–6.
crossref

12. Chan JY, Leung PC, Che CT, Fung KP. Protective effects of an herbal formulation of Radix Astragali, Radix Condonopsis and Cortex Lycii on streptoaotocin-induced apaptosis in pancreatic beta-cells: an implication for its treatment of diabetes mellitus. Phytother Rec. 2008; 22:190–6.
crossref

13. Cho SH, Park EJ, Kim EO, Choi SW. Study on the hypochlesterolemic and actioxidative effects of tyramine derivatives from the root bark of Lycii Radicis Cortex. Nut Rec Pract. 2011; 5:412–20.
crossref

14. Ye Z, Haung Q, Ni HX, Wang D. Cortex Lycii Radicis extracts improve insulin resistance and lipid metabolism in obese-diabetic rats. Phytother Res. 2008; 22:1665–70.
crossref

15. Jung YS, Park CH, Shin HC. Antioxidative effects of Lycium chinense Miller on cisplatin -induced nephrotoxicity in rats. Korean J Orent Int Med. 2014; 35:92–105.


16. Hou DX, Yanagita T, Uto T, Masuzaki S, Fujii M. Anthocyanidins inhibt cyclooxygenase-2 expression in LPS-evoked macrophages: structure-activity relationship and molecular mechanisms involved. Biochem Pharmacol. 2005; 70:417–25.
crossref

17. Jayaprakasam B, Vareed SK, Olson LK, Nair MG. Insulin secretion by bioactive anthocyanins and anthocyanidins present in fruits. J Agric Food Chem. 2005; 53:28–31.
crossref

18. Yamakoshi J, Kataoka S, Koga T, Ariga T. Proanthocyanidin-rich extract of grape seeds attenuated the development of aortic atherosclerosis in cholesterol-fed rabbits. Atherosclerosis. 1999; 142:139–49.
crossref

19. Ye X, Krohn RL, Liu W, Joshi SS, Kuszynski CA, McGinn TR, et al. The cytotoxic effects of n novel IH636 grape seed proanthocyanidin extract on cultured human cancer cells. Mol Cell Biochem. 1999; 196:99–108.
crossref

20. Ali SF, LeBel CP, Bondy SC. Reactive oxygen species formation as a biomarker of methylmercury and trimethyltin neurotoxicity. Neurotoxicology. 1992; 13:637–48.


21. McFarland KF, Catalano EW, Day JF, Thorpe SR, Baynes JW. Nonenzymatic glucosylation of serum proteins in diabetes mellitus. Diabetes. 1979; 28:1011–4.
crossref

22. Momose T, Yano Y, Ohashi K. Organic analysis. XLIV. A new deproteinizing agent for determination of blood sugar. Chem Pham Bull. 1963; 11:968–72.
crossref

23. Nakayama H, Mitsuhashi T, Kuwajima S, Aoki S, Kuroda Y, Itoh T, et al. Chemical detection of advanced glycation endproducts in lens crystallins from streptozocin-induced diabetic rat. Diabetes. 1993; 42:345–50.
crossref

24. Komatsu S. Extraction of nuclear proteins. Methods Mol Biol. 2007; 355:73–7.
crossref

25. Yokozawa T, Yamabe N, Kim HY, Kang KS, Hur JM, Park CH, et al. Protective effects of morroniside isolated from Corni Fructus against renal damage in streptozotocin-induced diabetic rats. Biol Pharm Bull. 2008; 31:1422–8.
crossref

26. Kim CM, Shin MG, Lee KS, Ahn DG. The encyclopedia of oriental herbal medicine. Seoul: Jungdam publishing group;2004. p. 3929–34.


27. Al-Malki AL, Sayed AA, El Rabey HA. Proanthocyanidin attenuateion of oxidative stress and NF-κB protects apolipoprotein E-deficient mice against diabetic nephropathy. Evidenc-Based Complementary and Alternative Medicine. 2013; 2013:1–8.


28. Rösen P, Nawroth PP, King G, Möller W, Tritschler HJ, Packer L. The role of oxidative stress in the onset and progression of diabetes and its complications: a summary of Congress Series sponsored by UNESCO-MCBN, the American Diabetes Association and the German Diabetes Society. Diabetes Metab Res Rev. 2001; 17:189–212.
crossref

29. Newsolme P, Haber EP, Hirabara SM, Rebelato EL, Procopio J, Morgan D, et al. Diabetes associated cell stress and dysfunction: role of mitochondrial and non-mitochondrial ROS production and activity. J Physiol. 2007; 583:9–24.
crossref

30. Kashihara N, Haruna Y, Kondeti VK, Kanwar YS. Oxidative stress in diabetic nephropathy. Curr Med Chem. 2010; 17:4256–69.
crossref

31. Tooke JE. Possible pathophysiological mechanisms for diabetic angiopathy in type 2 diabetes. J Diabetes Complications. 2000; 14:197–200.
crossref

32. Singh VP, Bali A, Singh N, Jaqqi AS. Advanced glycation endproducts and diabetic complications. Korean J Physiol Pharmacol. 2014; 18:1–14.
crossref

33. Schinzel R, Münch G, Heidland A, Sebecova K. Advanced glycation endproducts in end-stage renal disease and their removal. Nephron. 2001; 87:295–303.
crossref

34. Horie K, Miyata T, Maeda K, Miyata S, Suqiyama S, Sakai H, et al. Immunohistochemical colocalization of glycoxidation products and lipid peroxidation products in diabetic renal glomerular lesions. Implications for glycoxidative stress in the pathogenesis of diabetic nephropathy. J Clin Invest. 1997; 100:2995–3004.
crossref

35. Ceriello A, Bortolotti N, Pirisi M, Crescentini A, Tonutti L, Motz E, et al. Total plasma antioxidant capacity predicts thrombosis-prone status in NDDM patients. Diabetes Care. 1997; 20:1589–93.
crossref

36. Bierhaus A, Schiekofer S, Schwaninger M, Andrassy M, Humpert PM, Chen J, et al. Diabetes-associated sustained activation of the transcription factor nuclear factor-kappa B. Diabetes. 2001; 50:2792–808.
crossref

37. Nagi R, Ikeda K, Higashi T, Sano H, Jinnouchi Y, Araki T, et al. Hydroxyl radical mediates N epsilon-(carboxymethyl)lysine formation from Amadori product. Biochem Biophys Res Commun. 1997; 234:167–72.
crossref

38. Nagi R, Unno Y, Hayashi MC, Masuda S, Hayase F, Kinae N, et al. Peroxynitrite induces formation of N(epsilon)-(carboxymethyl) lysine by the caleavage of Amadori product and generation of glucosone and glyoxal from glucose: novel pathways for protein modification by peroxynitrite. Diabetes. 2002; 51:2833–89.
crossref

39. Wells-Knecht KJ, Zyzak DV, Litchfield JE, Thorpe SR, Baynes JW. Mechanism of autoxidative glycosylation: identification of glyoxal and arabinose as intermediates in the autoxidative modification of proteins by glucose. Biochemistry. 1995; 34:3702–9.
crossref

40. Koito W, Araki T, Horiuchi S, Nagai R. Conventional antibody against epsilon-(carboxymethyl) lysine (CML) shows cross-reaction to Nepsilon -(carboxyethyl)lysine (CEL): immnochemical quantification of CML with a specific antibody. J Biochem. 2004; 136:831–837.
crossref

41. Ahmed MU, Frye EB, Degenhardt TP, Thorpe SR, Baynes JW. Ne-(carboxyethyl)lysine, a product of the chemical modification of proteins by methylglyoxal, increase with age in human lens proteins. Biochem J. 1997; 324:565–70.
crossref

42. Lim AK, Tesch GH. Inflammation in diabetic nephropathy. Mediators Inflamm. 2012; 2012:1–12.
crossref

43. Lee JI, Burckart GJ. Nuclear factor kappa B: important transcription factor and therapeutic target. J Clin Pharmacol. 1998; 38:981–93.
crossref

44. Baldwin AS. NF-kappa B and I kappa B proteins: new discoveries and insights. Annu Rev Immunol. 1996; 14:649–83.
crossref

45. Sanchez AP, Sharma K. Transcription factors in the pathogenesis of diabetic nephropathy. Expert Rev Mol Med. 2009; 11:e13
crossref

46. Hess J, Anqel P, Schorpp-Kistner M. AP-1 subunits: quarrel and harmony among siblings. J Cell Sci. 2004; 117:5965–73.
crossref

Editorial office contact information
3F, #26-27 Gayang-dong, Gangseo-gu Seoul, 157-200 Seoul, Korea
The Society of Korean Medicine
Tel : +82-2-2658-3627   Fax : +82-2-2658-3631   E-mail : skom1953.journal@gmail.com
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Developed in M2PI