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


Advanced Search
JKM > Volume 36(3); 2015 > Article
Lee, Jang, Jeon, and Yim: Effects of Polyporus Herbal-acupuncture at KI10 on LPS-induced nephritis in rats

Abstract

Objectives:

The purpose of this study was to evaluate the effects of Polyporus Herbal-acupuncture(PO-HA) at KI10 (Umgok) on nephritis induced by lipopolysaccharide(LPS) in rats.

Methods:

Rats were allocated into normal, control, and 2 experimental groups. The rats in the control group were intra-peritoneally injected with LPS for nephritis induction. The rats in the groups of experiment 1 and experiment 2 were treated with Saline injection, and PO-HA, respectively at KI10 three times for a week and then intra-peritoneally injected with LPS. To evaluate the effects of PO-HA at KI10, WBC count in blood, creatine, tumor necrosis factor-alpha (TNF-α), cytokine-induced neutrophil chemoattractant 1(CINC-1) in serum, urinary volume, creatinine, total protein in urine, myeloperoxidase(MPO) in kidney were measured.

Results:

PO-HA at KI10 significantly suppressed the increase of WBC in blood, TNF-α, CINC-1 in serum, MPO in kidney of LPS-stimulated rats. PO-HA at KI10 significantly suppressed the increase creatinine, total protein in urine of LPS-stimulated rats.

Conclusions:

According to these results, it is postulated that PO-HA at KI10 has an anti-inflammatory and renal-protective effects on LPS-induced nephritis in rats. Therefore, it is suggested that PO-HA at KI10 may be an useful therapeutics for nephritis in clinical field after further researches.

Fig. 1.
Cytotoxicity of PO-HAS on rat liver cells.
Liver cells from normal SD rat were cultured in RPMI 1640 with 10% FBS medium for 72h with or without various concentrations of PO-HAS (Polyporus Herbal-acupuncture solution). The cell viability were measured by MTT assay.
Values represent the means ± SD of 3 independent experiments. Control : culture medium without PO-HAS
10%, 2.5%, 1% PO-HAS : culture medium with 10%, 2.5%, 1% PO-HAS respectively
jkm-36-3-73f1.tif
Fig. 2.
Effect of PO-HA on WBC count in blood of LPS-stimulated rats.
Data were expressed as mean ± SD (n=5).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
*** : p<0.001 compared to normal group by Kruskal-wallis test
††† : p<0.01 † : p<0.05 compared to LPS group by Kruskal -wallis test
# : p<0.05 compared to Saline group by Kruskal-wallis test
jkm-36-3-73f2.tif
Fig. 3.
Effects of PO-HA on serum creatinine level in LPS-stimulated rats.
Data were expressed as mean ± SD (n=5).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
*** : p<0.001 compared to normal group by Kruskal-wallis test
## : p<0.01 compared to Saline group by Kruskal-wallis test
jkm-36-3-73f3.tif
Fig. 4.
Effects of PO-HA on serum TNF-alpha level in LPS-stimulated rats.
Data were expressed as mean ± SD (n=5).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
*** : p<0.001 * : p<0.05 compared to normal group by Kruskal-wallis test
†† : p<0.01 compared to LPS group by Kruskal-wallis test
jkm-36-3-73f4.tif
Fig. 5.
Effects of PO-HA on serum CINC-1 level in LPS-stimulated rats.
Data were expressed as mean ± SD (n=5).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10 PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
*** : p<0.001 ** : p<0.01 compared to normal group by Kruskal -wallis test
†† : p<0.01 compared to LPS group by ANOVA test
jkm-36-3-73f5.tif
Fig. 6.
Effect of PO-HA on urinary volume in LPS-stimulated rats.
Data were expressed as mean ± SD (n=3).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
** : p<0.01 * : p<0.05 compared to normal group by Kruskal-wallis test
jkm-36-3-73f6.tif
Fig. 7.
Effects of PO-HA on urinary creatinine level in LPS-stimulated rats.
Data were expressed as mean ± SD (n=3).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
* : p<0.05 compared to normal group by Kruskal-wallis test
††† : p<0.001 compared to LPS group by Kruskal-wallis test
## : p<0.01 compared to Saline group by Kruskal-wallis test
jkm-36-3-73f7.tif
Fig. 8.
Effects of PO-HA on total protein level in urine of LPS-stimulated rats.
Data were expressed as mean ± SD (n=3).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
* : p<0.05 compared to normal group by Kruskal-wallis test
† : p<0.05 compared to LPS group by Kruskal-wallis test
jkm-36-3-73f8.tif
Fig. 9.
Effects of PO-HA on renal MPO level in LPS-stimulated rats.
Data were expressed as mean ± SD (n=5).
Normal : normal SD rat
LPS : LPS (2mg/kg) challenge
Saline : LPS (2mg/kg) challenge and Saline(200μℓ/rat) injection at KI10
PO-HA : LPS (2mg/kg) challenge and PO-HA(10%, 200μℓ/rat) at KI10
*** : p<0.001 compared to normal group by Kruskal-wallis test
†† : p<0.01 compared to LPS group by Kruskal-wallis test
jkm-36-3-73f9.tif
Scheme 1.
Manufacturing procedure of Polyporus Herbal-acupuncture Solution.
jkm-36-3-73s1.tif

참고문헌

1.. Du HK. Oriental Kidney System Internal Medicine. Seoul. Institute of the oriental science;(1993). p. 226p. 228p. 247p. 238-47. p. 326p. 334-6. p. 361-2. p. 454-9. p. 514-6.


2.. Du HK. Oriental Kidney System Internal Medicine. Seoul. Institute of the oriental science;(1993). p. 225p. 238-47. p. 256-7. p. 334-5. p. 359-401.


3.. Committee of Korean Textbook Publisher. Herbology. 6th ed. Seoul. Yeong Lim Sa;(1999). p. 304-5.


4.. Kim CM, Shin MK, Ahn DK, Lee KS. The encyclopedia of Oriental herbal medicine. Seoul. Jung Dam;(2004). p. 3700


5.. Sun, Y, & Yasukawa, K. New anti-inflammatory ergostane-type ecdysteroids from the sclerotium of Polyporus umbellatus. Bioorganic & Medicinal Chemistry Letters, (2008). 18, 3417-20.
crossref

6.. Ohsawa, T, Yukawa, M, Takao, C, Murayama, M, & Bando, H. Studies on constituents of fruit body of Polyporus umbellatus and their cytotoxic activity. Chem Pharm Bull, (1992). 40, 143-7.
crossref

7.. Oh, YH, Lee, UY, Lee, MW, Shim, MJ, & Lee, TS. Immnuo-modulatory and Antitumor Effect of Crude Polysaccharides Extracted from Sclerotium of Grifolia umbellata. The Korean Journal of Mycology, (2004). 32, 23-30.
crossref

8.. Zhang, Y, Liu, Y, & Yan, SC. Effect of Polyporus umbellatus polysaccahride on function of macrophages in the peritoneal cavities of mice with lesions. Cheih Ho Tsa Chih, (1991). 11, 211-5.


9.. May, L, & Yun, SC. Therapeutic investigation of Polyporus umbellatus polysaccahride on the children with pure immunity. J Traditional Chinese Medicine, (1990). 3, 168-9.


10.. Chang, YF, Liu, YY, & Yun, SC. Effect of Polyporus umbellatus polysaccahrides on macrophages of liver damaged mice. Intergrated J Chinese and Western Medicine, (1991). 11, 225-6.


11.. Xiong, LL. Therapeutic effect of combined therapy of Salvia miltiorrhizae and Polyporus umbellatus polysaccharide in the treatment of chronic hepatitis B. Cheih Ho Tsa Chih, (1993). 13, 516-7.


12.. Korean Pharmacopuncture institute. Aqua-acupuncture and clinical use. Seoul. Korean Pharmacopuncture institute;(1997). p. 1-5.


13.. Textbook Compilation Committee of Korean acupuncture & moxibustion medicine society. The acupuncture and Maxivustion (volume I). Seoul. JipMoonDang;(2001). p. 531-63. p. 1457-60.


14.. Choi, MS, Ko, HK, & Kim, CH. A study on aqua-acupuncture. Journal of Korean acupuncture & moxibustion medicine society, (1990). 7(1), 315-29.


15.. Meridian & Acupoint Compilation Committee of Korean Oriental Medical Colleges. Detail of meridians & acupoints (volume II) : a guidebook for college students. Daejeon. JongRyeoNaMu;(2012). p. 634-6.


16.. Kim, KM, Lee, H, Kang, HJ, Lee, YH, & Yim, YK. Anti-inflammatory Effect of Dianthi Semen Herbal-acupuncture at KI10 on nephritis in rats. Journal of Meridian & Acupoint, (2009). 26(1), 66-77.


17.. Park, BM, Hur, B, & Yim, YK. Anti-inflammatory Effect of Plantaginis Semen Herbal-acupuncture at KI10 on LPS-induced nephritis in rats. Journal of Meridian & Acupoint, (2009). 26(2), 127-43.


18.. Lee, JH, Kim, JH, & Kim, YI. Anti-inflammatory Effect of Benincasae Semen Herbal-acupuncture at KI10 on nephritis in rats. Journal of pharmacopuncture, (2010). 13(2), 51-65.
crossref

19.. Yoon, KS, Kang, JH, & Lee, H. Anti-inflammatory Effect on Desmodii Herba Pharmacopuncture at KI10 on Nephritis in Rats. Journal Of Korean Acupuncture & Moxibustion Medicine Society, (2011). 28(3), 43-54.


20.. Cho, E, Kang, JH, & Lee, H. Anti-inflammatory Effect of Akebiae Lignum Parmacopuncture at KI10 on LPS-induced Acute Nephritis in Rats. The Journal Of Korean Acupuncture & Moxibustion Medicine Society, (2012). 29(3), 41-53.


21.. Medzhitov, R, Preston-Hurlburt, P, & Janeway, CA. A human homologue of the Drosophila Toll protein signal activation of adaptive immunity. Nature, (1997). 388(6640), 394-7.
crossref

22.. Aderem, A, & Ulevitch, RJ. Toll-like receptors in the induction of the innate immune response. Nature, (2000). 406(6797), 782-7.
crossref

23.. Hoshino, K, Takeuchi, O, Kawai, T, Sanjo, H, Ogawa, T, & Takeda, Y, et al. Toll-like receptor 4(TLR4)-deficient mice are hyporesponsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product. J immunol, (1999). 162(7), 3749-52.


24.. Baumgartner, J-D, & Cohen, J. Septic shock Pathogenesis. Lancet, (1991). 338, 732-6.
crossref

25.. Ohmori, Y, & Hamilton, TA. A macrophage LPS-inducible early gene encodes the murine homologue of IP-10. Biochem Biophys Res Commun, (1990). 168, 1261-7.
crossref

26.. Tannenbaum, CS, Koemer, TJ, Jansen, MM, & Hamilton, TA. Characteriation of Lipopolysaccharide-induced macrophage gene expression. J immunol, (1988). 140, 3640-5.


27.. Abbas AK, Lichtman AH, Pillai S. Cellular and Molecular Immunology. 4th ed. KangJS. Seoul. PanMunSa;(2002). p. 23-40. p. 240-3. p. 567-8.


28.. Harada, A, Sekido, N, Akahoshi, T, Wada, T, Mukaida, N, & Matsushima, K. Essential involvement of interleukin-8(IL-8) in acute inflammation. Journal of Leukocyte Biology, (1994). 56, 559-64.


29.. Matsushima, K, Morishita, K, Yoshimura, T, Lavu, S, Kobayashi, Y, & Lew, W, et al. Molecular cloning of a human monocyte-derived neutrophil chemotactic factor (MDNCF) and the induction of MDNCF mRNA by interleukin 1 and tumor necrosis factor. J. Exp. Med, (1988). 167, 1883-93.
crossref

30.. Strieter, RM, Kunkel, SL, Showell, HJ, Remick, DG, Phan, SH, & Ward, PA, et al. Endothelial cell gene expression of a neutrophil chemotactic factor by TNF-alpha, LPS, and IL-1 beta. Science, (1989). 243, 1467-9.
crossref

31.. Sekido, N, Mukaida, N, Harada, A, Nakanishi, I, Watanabe, Y, & Matsushima, K. Prevention of lung reperfusion injury in rabbits by a monoclonal antibody against interleukin-8. Nature, (1993). 365, 654-7.
crossref

32.. Krawisz, JE, Sharon, P, & Stenson, WF. Quantitive assay for acute intestinal inflammation based on myeloperoxidase activity. Assessment of inflammation in rat and hamster models. Gastroenterology, (1984). 87, 1344-55.


33.. Song KY, Ji JK, Ham UK. Core Pathology. Seoul. Korea Medical Book Publishing company;(1998). p. 79-80. p. 573p. 576-80.


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