Open Access

Ginsenoside Rg3 induces ginsenoside Rb1-comparable cardioprotective effects independent of reducing blood pressure in spontaneously hypertensive rats

  • Authors:
    • Yichuan Jiang
    • Min Li
    • Zeyuan Lu
    • Yuchen Wang
    • Xiaofeng Yu
    • Dayun Sui
    • Li Fu
  • View Affiliations

  • Published online on: September 22, 2017     https://doi.org/10.3892/etm.2017.5198
  • Pages: 4977-4985
  • Copyright: © Jiang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Ginsenoside Rg3 (Rg3) is a rare type of ginsenoside used as an anti-tumor medicine in China. Ginsenoside Rb1 (Rb1), which exhibits protective effects on the cardiovascular system, is similar to Rg3 in chemical structure. In the present study, Rb1 and Rg3 were administered for 6 weeks to spontaneously hypertensive rats (SHR) and their cardioprotective effects were assessed. According to echocardiography and histopathological examinations, the decrease in cardiac function and ventricular remodeling that occurred in SHR rats were attenuated by Rb1 and Rg3. However, tail-cuff blood pressure measurements indicated that Rb1 and Rg3 did not reduce blood pressure in SHR rats. The cardioprotective effects of Rb1 and Rg3 occurred independently of blood pressure reduction. Furthermore, immunohistochemistry (IHC) revealed that renin angiotensin system (RAS) activity in the myocardium of SHR was significantly attenuated by Rb1 and Rg3, whereas ELISA identified no significant changes of RAS activity in the serum. The results of IHC and reverse transcription-quantitative polymerase chain reaction demonstrated that levels of transforming growth factor β1, tumor necrosis factor-α, interleukin-6, interleukin-1 and endothelian-1 in the myocardium of SHR rats were reduced following Rb1 and Rg3 treatment. This may be due to the attenuation of RAS activity in the myocardium and the mechanisms of the cardioprotective effects of Rb1 and Rg3.

Introduction

Ginsenosides, which are extracted from ginseng (Panax ginseng), American ginseng (Panax quinquefolium) and notoginseng (Panax notoginseng), exhibit a variety of pharmacological activities, including cardiovascular protective (17), neuroprotective (810) and anti-tumor effects (1116). Ginsenoside Rb1 (Rb1) is one of the monomers contained in total ginsenosides (extracted from sun-cured ginseng) whereas ginsenoside Rg3 (Rg3), a particularly rare ginsenoside, is obtained from other ginsenosides by heat treatment during ginseng processing (17). Chemical (17) or biological (18,19) methods have also been used to transform other ginsenosides, including Rb1, into Rg3.

Previous studies have demonstrated that Rb1 exhibits beneficial effects on the cardiovascular system. It is able to attenuate myocardial ischemia, reperfusion injury (2) and ventricular remodeling (1,5). The chemical structure of Rg3 is similar to that of Rb1 (Fig. 1); however Rg3 exhibits strong anti-tumor activity (12,13,15,16), which Rb1 does not, meaning that it may be used to treat patients with tumors. The Shenyi Capsule, which is produced by Jilin Yatai Pharmaceutical Co., Ltd., is a widely used anti-tumor medication in China and its principal component is Rg3. Although the anti-tumor activity of Rg3 has been well documented, to the best of our knowledge, it remains unknown whether Rg3 induces the same beneficial effects on the cardiovascular system that Rb1 does. Our group is currently undertaking a long-term study in which the effects of various ginsenosides, including Rb1 and Rg3, are assessed in various animal models of chronic disease, such as hypertension, hyperlipemia and diabetes.

The spontaneously hypertensive rat (SHR) is a widely used animal model of hypertension. Angiotensin II (Ang II) levels in the blood and myocardial tissue are abnormally higher in SHR than in healthy Wistar-Kyoto (WKY) rats. Increased Ang II levels cause progressive hypertension, myocardial fibrosis and may even induce ventricular remodeling, resulting in heart failure (20,21). The aim of the present study was to assess and compare the effects of Rb1 and Rg3 and determine whether Rg3 exhibits protective effects on the cardiovascular system in SHR rats.

Materials and methods

Reagents

Rb1 (95% purity) was obtained from Dr. Yanping Chen at the Department of Natural Medicinal Chemistry, School of Chemistry, Jilin University (Jilin, China) and dissolved in double-distilled water (ddH2O) prior to use. Rg3 (95% purity) was obtained from Jilin Yatai Pharmaceutical Co., Ltd. (Changchun, China) and suspended in 0.5% sodium carboxymethyl cellulose solution for use. All other chemicals were analytical reagents.

Animals and treatments

A total of 24 SHR and 8 WKY rats (male, 16-17-week-old, 250-300 g) were purchased from Vital River Laboratories Co., Ltd. (Beijing, China). All rats were kept in a specific pathogen-free experimental animal workshop (25°C, 10/14-h light/dark cycle), and had free access to food and water. Experiments were performed in accordance with the Guide for the Care and Use of Laboratory Animals of Jilin University and approved by the Ethics Committee of Jilin University.

The rats were randomly divided into 4 groups (each, n=8): i) A WKY group, consisting of WKY rats orally administered ddH2O; ii) a SHR group, consisting of SHR rats orally administered ddH2O; iii) a Rb1 group consisting of SHR rats orally administered 20 mg/kg Rb1; and iv) a Rg3 group Rg3 consisting of SHR rats orally administered 20 mg/kg Rg3. All treatments were administered once a day over 42 consecutive days.

After treatment for 6 weeks with ddH2O or ginsenosides, all rats were anesthetized with chloral hydrate (300 mg/kg, intraperitoneally), and blood samples were obtained from the abdominal aorta before the rats were sacrificed. Hearts were obtained and weighed after the rats were sacrificed, and myocardium tissue samples were then fixed in 4% buffered paraformaldehyde solution (25°C, 24 h) for histopathological examination or frozen in liquid nitrogen and stored at −80°C prior to reverse transcription-quantitative polymerase chain reaction (RT-qPCR).

Blood pressure measurement

The systolic blood pressure (SBP), diastolic blood pressure (DBP) and pulse pressure (PP) of rats were measured using the tail-cuff method and a small animal sphygmomanometer (BP-2010A; Softron Biotechnology Ltd., Beijing, China) following a previously described protocol (22) on the first and the last days of the 6-week treatment.

Echocardiography

On the first and last days of the 6-week treatment, transthoracic echocardiography was performed as previously described (23), using a standard setting with a 10S transducer (Vivid-i; GE Healthcare, Chicago, IL, USA). Animals were anesthetized with chloral hydrate (300 mg/kg, intraperitoneally) and two-dimensional and M-mode echocardiographic measurements were conducted. A short-axis two-dimensional image of the left ventricle was obtained at the position of the papillary muscles. Subsequently, M-mode images were acquired at a sweep speed of 100 mm/s and digitally stored. The left ventricular internal dimension at diastole (LVIDd) and left ventricular internal dimension at systole (LVIDs) were acquired from M-mode images; subsequently, left ventricular fractional shortening (FS) and left ventricular ejection fraction (EF) were calculated automatically by the equipment. The parameters were measured by an experienced echocardiographer blinded to the treatment groups.

Assay of the angiotensin converting enzyme (ACE) and Ang II levels in the serum

Blood samples were collected and left at room temperature for 2 h to allow complete clotting and then centrifuged at 1,500 × g, 4°C for 15 min. The serum was removed and stored at −80°C prior to ELISA. ACE (CSB-E04490r) and Ang II (CSB-E04494r) ELISA kits were purchased from Cusabio Biotech Co., Ltd. (Wuhan, China) and the assays were completed by this company.

Histopathological examination

Myocardial tissue samples were fixed in 4% buffered paraformaldehyde solution and then embedded in paraffin. Paraffin-embedded sections 4-μm thick were stained with hematoxylin and eosin (H&E) and Masson trichrome stain. Sections were examined using a Nikon E100 light microscope (Nikon Corporation, Tokyo, Japan) and photomicrograph images were captured.

Immunohistochemistry (IHC)

Primary antibodies against ACE (bs-0439R), Ang II (bs-0587R), Ang II receptor type 1 (AT1, bs-0438R) and transforming growth factor β1 (TGF-β1, bs-0103R) were purchased from Bioss Antibodies (Beijing, China). Peroxidase-conjugated goat anti-rabbit IgG (ZB-2301), DAB kit (ZLI-9018) and two step rabbit IHC kit (PV-6001) were purchased from ZSGB-BIO (Beijing, China). IHC was performed following the manufacturer's protocols of the IHC kit and DAB kit. Photomicrograph images were then captured, and Image Pro Plus 6.0 (Media Cybernetics, Inc., Rockville, MD, USA) was used for image analysis.

RNA preparation and RT-qPCR

Total RNA was isolated from frozen myocardium tissue samples using TRIzol reagent (Thermo Fisher Scientific, Inc., Waltham, MA, USA) following the manufacturer's protocol. Total RNA was reverse-transcribed and qPCR was conducted using the TransScript Green Two-Step qRT-PCR SuperMix (TransGen Biotech Co., Ltd., Beijing, China) on the Stratagene Mx3000P (Agilent Technologies, Inc., Santa Clara, CA, USA) and following the manufacturer's protocol (94°C for 5 sec, 60°C for 15 sec and 72°C for 10 sec, 40 cycles). The relative fold changes in the mRNA levels of the target genes were determined using the 2−ΔΔCq method (24) and β-actin was used as a housekeeping gene. Primer sequences are provided in Table I.

Table I.

Primer sequences of TNF-α, IL-6, IL-1β, ET-1 and β-actin.

Table I.

Primer sequences of TNF-α, IL-6, IL-1β, ET-1 and β-actin.

Primer nameSequences
β-actinForward: 5′-GATCAAGATCATTGCTCCTCCTG-3′
Reverse: 5′-AGGGTGTAAAACGCAGCTCA-3′
TNF-αForward: 5′-GTCGTAGCAAACCACCAAGC-3′
Reverse: 5′-TGTGGGTGAGGAGCACGTAG-3′
IL-6Forward: 5′-TGTATGAACAGCGATGATG-3′
Reverse: 5′-AGAAGACCAGAGCAGATT-3′
IL-1βForward: 5′-GCAATGGTCGGGACATAGTT-3′
Reverse: 5′-AGACCTGACTTGGCAGAGG-3′
ET-1Forward: 5′-GCTCCTCCTTGATGGACAA-3′
Reverse: 5′-TTTGGTGAGCACACTGGC-3′

[i] TNF-α, tumor necrosis factor-α; IL, interleukin-6; IL-1β, interleukin-1β; ET-1, endothelin-1.

Statistical analysis

SPSS 15.0 statistical software (SPSS, Inc., Chicago, IL, USA) was used for statistical analysis. All data are expressed as the mean ± standard deviation. One-way analysis of variance with Tukey's post hoc test was used to analyze differences among groups and P<0.05 was considered to indicate a statistically significant difference.

Results

Effects of Rb1 and Rg3 on cardiac structure and function

The effects of Rb1 and Rg3 on cardiac structure and function were evaluated using echocardiography. As depicted in Fig. 2, compared with the WKY group prior to the 6-week treatment, the three groups of SHR rats exhibited slight cardiac function injury; they had a significantly lower FS and EF compared with the WKY group (P<0.05; Fig. 2D and E). However, LVIDd and LVIDs were similar among all groups, indicating that the cardiac structure of SHR rats was unaffected prior to the 6-week treatment.

Following the 6-week treatment, the FS and EF of the three SHR groups were all significantly reduced compared with the WKY group (P<0.05). However, the FS and EF of the Rb1 and Rg3 groups were significantly higher than those of the SHR group (P<0.05; Fig. 2D and E). Rb1 and Rg3 also exhibited protective effects on cardiac structure. Following treatment, the LVIDd and LVIDs of the SHR group were significantly higher than those of the WKY group (P<0.05); however, those of the Rb1 and Rg3 groups were significantly lower than the SHR group and did not differ significantly between those of the WKY group (Fig. 2B and C). Notably, the cardiac protective effects of Rb1 and Rg3 were comparable.

Effects of Rb1 and Rg3 on blood pressure

Rb1 and Rg3 did not significantly affect the blood pressure of SHR rats. The SBP and DBP of the three groups of SHR rats were all significantly higher than the WKY group prior to and following 6-week treatment (P<0.05) and there was no significant difference in blood pressure between the SHR group and the Rb1 or Rg3 groups (Fig. 3A and B). Regarding PP, there were no significant differences between any groups prior to or following treatment (Fig. 3C).

Effects of Rb1 and Rg3 on the cardiac weight index (CWI)

The body weights and heart weights of all four groups are presented in Fig. 3D and E. CWI was subsequently calculated using the following formula: Heart weight/body weight. The CWI of the SHR group was significantly higher than that of the WKY group (P<0.05), while those of groups Rb1 and Rg3 were significantly lower than the SHR group (P<0.05; Fig. 3F). This result demonstrated that hypertension induces cardiac structural changes and that Rb1 and Rg3 significantly attenuate these changes.

Effects of Rb1 and Rg3 on renin angiotensin system (RAS) activity

Rb1 and Rg3 had no significant effects on RAS activity in the serum. ACE and Ang II levels of the three SHR groups were all significantly higher than those of the WKY group (P<0.05) and there were no significant differences between ACE and Ang II levels between the three SHR groups (Fig. 3G and H). This may explain why Rb1 and Rg3 did not significantly reduce blood pressure in SHR rats.

Effects of Rb1 and Rg3 on myocardium histology

Representative H&E and Masson staining histology photomicrographs are presented in Fig. 4. According to the H&E photomicrographs, myocardium tissues from the SHR group exhibited increased myocardial cell size, myocardial structural disorder and intercellular space dilatation, which are the typical pathological changes of ventricular remodeling induced by hypertension. Inflammatory cell infiltration was also observed. The Masson photomicrographs indicated increased collagen deposition (blue area) in the SHR group compared with the WKY group. However, treatment with Rb1 and Rg3 markedly improved all these histopathological changes.

Effects of Rb1 and Rg3 on RAS activity and TGF-β1 levels in the myocardium

The expression of ACE, Ang II, AT1 and TGF-β1 in the myocardium was evaluated using IHC. Representative photomicrographs are presented in Fig. 5A and quantitative results are presented in Fig. 5B-E. Compared with the WKY group, levels of ACE, Ang II, AT1 and TGF-β1 were significantly increased in myocardium samples from the SHR group (all P<0.05). However, these increases were significantly attenuated following treatment with Rb1 and Rg3 (all P<0.05). Indeed, the expression of Ang II and TGF-β1 in the Rb1 and Rg3 groups did not differ significantly between that of the WKY group (Fig. 5D and E). The downregulation of local RAS activity in the myocardium reduced the expression of TGF-β1, which is also a key factor to myocardial fibrosis.

Effects of Rb1 and Rg3 on levels of inflammatory factors and ET-1 in the myocardium

Levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-1β (IL-1β) and ET-1 mRNA were measured (Fig. 6). In the SHR group, the expression of TNF-α, IL-6, IL-1β and ET-1 mRNA were all significantly higher than in the WKY group (all P<0.05). However, in the Rb1 and Rg3 groups, the levels of all four mRNAs were all significantly lower than the SHR group (P<0.05). These results suggest that Rb1 and Rg3 may attenuate inflammation and endothelial injury in the myocardium.

Discussion

One of the main mechanisms by which hypertension arises in SHR is congenital abnormal RAS activation, which is similar to what occurs in human essential hypertension (25). Therefore, ACE inhibitors and AT1 receptor blockers are currently the most popular antihypertensive medicines. Ang II, the key factor of the RAS, increases blood pressure and induces inflammation, endothelial injury and fibrosis in various organs (26).

Ang II is an independent factor that causes myocardial fibrosis and ventricular remodeling, regardless whether it has induced hypertension or not (27). A high amount of RAS activity causes hypertension, whereas high Ang II levels in the myocardium increase TGF-β1 expression, which may promote fibroblast proliferation and collagen deposition (28). High levels of Ang II may also increase levels of TNF-α, IL-6, IL-1β and ET-1, which are all closely associated with cardiovascular injury (26) and may contribute to myocardial fibrosis and ventricular remodeling.

The results of the present study indicated that Rb1 and Rg3 attenuated cardiac function and structural changes in SHR but did not reduce blood pressure (Fig. 7). RAS activity was attenuated in the myocardium of the Rb1 and Rg3 groups, whereas RAS activity in the serum remained high. The mechanism of this action remains unknown; something in the myocardium, for example, angiotensin-converting enzyme 2, an enzyme that degrades Ang II into Ang 1–7 (27), may be activated by Rb1 or Rg3 to degrade Ang II. However, further studies are required to determine the exact mechanism of action by which this occurs.

As RAS activity was attenuated in the myocardium, levels of TGF-β1, TNF-α, IL-6, IL-1β and ET-1 were all reduced following treatment with Rg3 and Rb1, although blood pressure remained high. Furthermore, Rb1 and Rg3 were able to protect against myocardial fibrosis and ventricular remodeling in the heart. According to the results of histopathology and echocardiography, the cardiovascular protective effect of Rg3 is similar to that of Rb1 in SHR. However, further studies are required to determine the cardioprotective effects of Rg3 in other models of cardiovascular injury, particularly in adriamycin induced heart failure (29).

Rg3 is a widely used anti-tumor medicine in China and it is important to determine whether it also exhibits protective effects on the cardiovascular system. A number of first-line chemotherapy agents, including adriamycin, are cardiotoxic (30). As Rg3 exhibits cardioprotective effects, it is worth determining whether Rg3 attenuates the cardiotoxicity of chemotherapeutic agents when they are used together. This may facilitate the development of safer and more efficient treatment protocols for chemotherapy.

In conclusion, the present study indicated that hypertension and high RAS activity in the myocardium induce cardiac structural and functional changes, which may be attenuated by Rg3 as well as Rb1, independent of reducing blood pressure. Furthermore, the mechanism of these protective effects of Rg3 on the cardiovascular system may be associated with the attenuation of RAS activity in the myocardium. Therefore, Rg3 may also attenuate inflammation, endothelial injury and fibrosis. Therefore, the results of the present study demonstrated that Rg3 exhibits similar cardiovascular protective effects to Rb1 independent of reducing blood pressure in SHR rats.

Acknowledgements

The present study was supported by the National Natural Science Foundation of China (grant no. 81473378) and Outstanding Doctoral Cultivation Program of Norman Bethune Health Science Center of Jilin University (2014).

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Spandidos Publications style
Jiang Y, Li M, Lu Z, Wang Y, Yu X, Sui D and Fu L: Ginsenoside Rg3 induces ginsenoside Rb1-comparable cardioprotective effects independent of reducing blood pressure in spontaneously hypertensive rats. Exp Ther Med 14: 4977-4985, 2017.
APA
Jiang, Y., Li, M., Lu, Z., Wang, Y., Yu, X., Sui, D., & Fu, L. (2017). Ginsenoside Rg3 induces ginsenoside Rb1-comparable cardioprotective effects independent of reducing blood pressure in spontaneously hypertensive rats. Experimental and Therapeutic Medicine, 14, 4977-4985. https://doi.org/10.3892/etm.2017.5198
MLA
Jiang, Y., Li, M., Lu, Z., Wang, Y., Yu, X., Sui, D., Fu, L."Ginsenoside Rg3 induces ginsenoside Rb1-comparable cardioprotective effects independent of reducing blood pressure in spontaneously hypertensive rats". Experimental and Therapeutic Medicine 14.5 (2017): 4977-4985.
Chicago
Jiang, Y., Li, M., Lu, Z., Wang, Y., Yu, X., Sui, D., Fu, L."Ginsenoside Rg3 induces ginsenoside Rb1-comparable cardioprotective effects independent of reducing blood pressure in spontaneously hypertensive rats". Experimental and Therapeutic Medicine 14, no. 5 (2017): 4977-4985. https://doi.org/10.3892/etm.2017.5198