Skip to main content
Erschienen in: Journal of Natural Medicines 2/2019

01.03.2019 | Original Paper

Sakuranetin downregulates inducible nitric oxide synthase expression by affecting interleukin-1 receptor and CCAAT/enhancer-binding protein β

verfasst von: Yuko Yamauchi, Tetsuya Okuyama, Toshinari Ishii, Tadayoshi Okumura, Yukinobu Ikeya, Mikio Nishizawa

Erschienen in: Journal of Natural Medicines | Ausgabe 2/2019

Einloggen, um Zugang zu erhalten

Abstract

Pruni Cortex is a herbal drug from the bark of the Japanese flowering cherries, Prunus jamasakura or Prunus verecunda, and is included in the traditional Japanese herbal (Kampo) formula Jumihaidokuto, which is administered orally to patients suffering from inflammatory skin diseases. The flavanones contained in Pruni Cortex (e.g., sakuranetin and naringenin) have potent anti-inflammatory, anti-allergic, and anti-microbial activities. Although the effects of Pruni Cortex on skin disease have been well studied, reports regarding its pharmacological effects on the liver are limited. In this study, we extracted the bark of Prunus jamasakura and purified it to isolate the pharmacologically active constituents by monitoring nitric oxide (NO) production in rat hepatocytes that were treated with the pro-inflammatory cytokine, interleukin (IL)-1β. Sakuranetin and (−)-naringenin, which were present in an ethyl acetate-soluble fraction of the bark extract, significantly inhibited NO induction and inducible nitric oxide synthase (iNOS) expression. These two flavanones decreased the expression of type 1 IL-1 receptor gene and phosphorylation of Akt, also known as protein kinase B, which is regulated by phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K). Furthermore, sakuranetin decreased the phosphorylation of the activator isoforms of CCAAT/enhancer-binding protein β (C/EBPβ), which synergistically activates the transcription of the iNOS gene with nuclear factor κB (NF-κB). Therefore, sakuranetin inhibited the co-activating activity of C/EBPβ with NF-κB, leading to the suppression of iNOS gene expression in hepatocytes. Taken together, sakuranetin in Pruni Cortex downregulated the iNOS gene by inhibiting PI3K/Akt signal transduction and the phosphorylation of C/EBPβ. These results imply that sakuranetin may be primarily responsible for the anti-inflammatory effects of Pruni Cortex in the liver.
Literatur
1.
Zurück zum Zitat The Committee on the Japanese Pharmacopoeia (2016) The Japanese pharmacopoeia, 17th edn. The Minister of Health, Labour and Welfare, Japan The Committee on the Japanese Pharmacopoeia (2016) The Japanese pharmacopoeia, 17th edn. The Minister of Health, Labour and Welfare, Japan
2.
Zurück zum Zitat Tohno H, Horii C, Fuse T, Okonogi A, Yomoda S (2010) Evaluation of estrogen receptor beta binding of pruni cortex and its constituents. Yakugaku Zasshi 130:989–997CrossRefPubMed Tohno H, Horii C, Fuse T, Okonogi A, Yomoda S (2010) Evaluation of estrogen receptor beta binding of pruni cortex and its constituents. Yakugaku Zasshi 130:989–997CrossRefPubMed
3.
Zurück zum Zitat Izuo M (2004) Medical history: Seishu Hanaoka and his success in breast cancer surgery under general anesthesia two hundred years ago. Breast Cancer 11:319–324CrossRefPubMed Izuo M (2004) Medical history: Seishu Hanaoka and his success in breast cancer surgery under general anesthesia two hundred years ago. Breast Cancer 11:319–324CrossRefPubMed
4.
Zurück zum Zitat Mizawa M, Makino T, Inami C, Shimizu T (2016) Jumihaidokuto (Shi-Wei-Ba-Du-Tang), a Kampo formula, decreases the disease activity of palmoplantar pustulosis. Dermatol Res Pract 2016:4060673CrossRefPubMedPubMedCentral Mizawa M, Makino T, Inami C, Shimizu T (2016) Jumihaidokuto (Shi-Wei-Ba-Du-Tang), a Kampo formula, decreases the disease activity of palmoplantar pustulosis. Dermatol Res Pract 2016:4060673CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Matsuoka N, Ikeda T, El-Aasr M, Manabe H, Murakami Y, Deguchi H, Nohara T (2011) Study of the chemical constituents of Pruni cortex and its related parts. J Nat Med 65:166–171CrossRefPubMed Matsuoka N, Ikeda T, El-Aasr M, Manabe H, Murakami Y, Deguchi H, Nohara T (2011) Study of the chemical constituents of Pruni cortex and its related parts. J Nat Med 65:166–171CrossRefPubMed
6.
Zurück zum Zitat Shimizu T, Lin F, Hasegawa M, Okada K, Nojiri H, Yamane H (2012) Purification and identification of naringenin 7-O-methyltransferase, a key enzyme in biosynthesis of flavonoid phytoalexin sakuranetin in rice. J Biol Chem 287:19315–19325CrossRefPubMedPubMedCentral Shimizu T, Lin F, Hasegawa M, Okada K, Nojiri H, Yamane H (2012) Purification and identification of naringenin 7-O-methyltransferase, a key enzyme in biosynthesis of flavonoid phytoalexin sakuranetin in rice. J Biol Chem 287:19315–19325CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Watanabe K, Karuppagounder V, Arumugam S, Thandavarayan RA, Pitchaimani V, Sreedhar R, Afrin R, Harima M, Suzuki H, Suzuki K, Nakamura T, Nomoto M, Miyashita S, Fukumoto K, Ueno K (2015) Pruni cortex ameliorates skin inflammation possibly through HMGB1–NF-κB pathway in house dust mite induced atopic dermatitis NC/Nga transgenic mice. J Clin Biochem Nutr 56:186–194CrossRefPubMedPubMedCentral Watanabe K, Karuppagounder V, Arumugam S, Thandavarayan RA, Pitchaimani V, Sreedhar R, Afrin R, Harima M, Suzuki H, Suzuki K, Nakamura T, Nomoto M, Miyashita S, Fukumoto K, Ueno K (2015) Pruni cortex ameliorates skin inflammation possibly through HMGB1–NF-κB pathway in house dust mite induced atopic dermatitis NC/Nga transgenic mice. J Clin Biochem Nutr 56:186–194CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Drira R, Sakamoto K (2016) Sakuranetin induces melanogenesis in B16BL6 melanoma cells through inhibition of ERK and PI3K/AKT signaling pathways. Phytother Res 30:997–1002CrossRefPubMed Drira R, Sakamoto K (2016) Sakuranetin induces melanogenesis in B16BL6 melanoma cells through inhibition of ERK and PI3K/AKT signaling pathways. Phytother Res 30:997–1002CrossRefPubMed
9.
Zurück zum Zitat Toledo AC, Sakoda CP, Perini A, Pinheiro NM, Magalhães RM, Grecco S, Tibério IF, Câmara NO, Martins MA, Lago JH, Prado CM (2013) Flavonone treatment reverses airway inflammation and remodelling in an asthma murine model. Br J Pharmacol 168:1736–1749CrossRefPubMedPubMedCentral Toledo AC, Sakoda CP, Perini A, Pinheiro NM, Magalhães RM, Grecco S, Tibério IF, Câmara NO, Martins MA, Lago JH, Prado CM (2013) Flavonone treatment reverses airway inflammation and remodelling in an asthma murine model. Br J Pharmacol 168:1736–1749CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Tsukada J, Yoshida Y, Kominato Y, Auron PE (2011) The CCAAT/enhancer (C/EBP) family of basic-leucine zipper (bZIP) transcription factors is a multifaceted highly-regulated system for gene regulation. Cytokine 54:6–19CrossRefPubMed Tsukada J, Yoshida Y, Kominato Y, Auron PE (2011) The CCAAT/enhancer (C/EBP) family of basic-leucine zipper (bZIP) transcription factors is a multifaceted highly-regulated system for gene regulation. Cytokine 54:6–19CrossRefPubMed
12.
13.
Zurück zum Zitat Kitade H, Sakitani K, Inoue K, Masu Y, Kawada N, Hiramatsu Y, Kamiyama Y, Okumura T, Ito S (1996) Interleukin 1β markedly stimulates nitric oxide formation in the absence of other cytokines or lipopolysaccharide in primary cultured rat hepatocytes but not in Kupffer cells. Hepatology 23:797–802PubMed Kitade H, Sakitani K, Inoue K, Masu Y, Kawada N, Hiramatsu Y, Kamiyama Y, Okumura T, Ito S (1996) Interleukin 1β markedly stimulates nitric oxide formation in the absence of other cytokines or lipopolysaccharide in primary cultured rat hepatocytes but not in Kupffer cells. Hepatology 23:797–802PubMed
14.
Zurück zum Zitat Teshima S, Nakanishi H, Nishizawa M, Kitagawa K, Kaibori M, Yamada M, Habara K, Kwon AH, Kamiyama Y, Ito S, Okumura T (2004) Up-regulation of IL-1 receptor through PI3K/Akt is essential for the induction of iNOS gene expression in hepatocytes. J Hepatol 40:616–623CrossRefPubMed Teshima S, Nakanishi H, Nishizawa M, Kitagawa K, Kaibori M, Yamada M, Habara K, Kwon AH, Kamiyama Y, Ito S, Okumura T (2004) Up-regulation of IL-1 receptor through PI3K/Akt is essential for the induction of iNOS gene expression in hepatocytes. J Hepatol 40:616–623CrossRefPubMed
15.
Zurück zum Zitat Inaba H, Yoshigai E, Okuyama T, Murakoshi M, Sugiyama K, Nishino H, Nishizawa M (2015) Antipyretic analgesic drugs have different mechanisms for regulation of the expression of inducible nitric oxide synthase in hepatocytes and macrophages. Nitric Oxide 44:61–70CrossRefPubMed Inaba H, Yoshigai E, Okuyama T, Murakoshi M, Sugiyama K, Nishino H, Nishizawa M (2015) Antipyretic analgesic drugs have different mechanisms for regulation of the expression of inducible nitric oxide synthase in hepatocytes and macrophages. Nitric Oxide 44:61–70CrossRefPubMed
16.
Zurück zum Zitat Miki H, Tokuhara K, Oishi M, Nakatake R, Tanaka Y, Kaibori M, Nishizawa M, Okumura T, Kon M (2016) Japanese Kampo Saireito has a liver-protective effect through the inhibition of inducible nitric oxide synthase induction in primary cultured rat hepatocytes. JPEN J Parenter Enteral Nutr 40:1033–1041CrossRefPubMed Miki H, Tokuhara K, Oishi M, Nakatake R, Tanaka Y, Kaibori M, Nishizawa M, Okumura T, Kon M (2016) Japanese Kampo Saireito has a liver-protective effect through the inhibition of inducible nitric oxide synthase induction in primary cultured rat hepatocytes. JPEN J Parenter Enteral Nutr 40:1033–1041CrossRefPubMed
17.
Zurück zum Zitat Yoshigai E, Machida T, Okuyama T, Mori M, Murase H, Yamanishi R, Okumura T, Ikeya Y, Nishino H, Nishizawa M (2013) Citrus nobiletin suppresses inducible nitric oxide synthase gene expression in interleukin-1β-treated hepatocytes. Biochem Biophys Res Commun 439:54–59CrossRefPubMed Yoshigai E, Machida T, Okuyama T, Mori M, Murase H, Yamanishi R, Okumura T, Ikeya Y, Nishino H, Nishizawa M (2013) Citrus nobiletin suppresses inducible nitric oxide synthase gene expression in interleukin-1β-treated hepatocytes. Biochem Biophys Res Commun 439:54–59CrossRefPubMed
18.
Zurück zum Zitat Takimoto Y, Qian HY, Yoshigai E, Okumura T, Ikeya Y, Nishizawa M (2013) Gomisin N in the herbal drug gomishi (Schisandra chinensis) suppresses inducible nitric oxide synthase gene via C/EBPβ and NF-κB in rat hepatocytes. Nitric Oxide 28:47–56CrossRefPubMed Takimoto Y, Qian HY, Yoshigai E, Okumura T, Ikeya Y, Nishizawa M (2013) Gomisin N in the herbal drug gomishi (Schisandra chinensis) suppresses inducible nitric oxide synthase gene via C/EBPβ and NF-κB in rat hepatocytes. Nitric Oxide 28:47–56CrossRefPubMed
19.
Zurück zum Zitat Fujii A, Okuyama T, Wakame K, Okumura T, Ikeya Y, Nishizawa M (2017) Identification of anti-inflammatory constituents in Phellodendri Cortex and Coptidis Rhizoma by monitoring the suppression of nitric oxide production. J Nat Med 71:745–756CrossRefPubMed Fujii A, Okuyama T, Wakame K, Okumura T, Ikeya Y, Nishizawa M (2017) Identification of anti-inflammatory constituents in Phellodendri Cortex and Coptidis Rhizoma by monitoring the suppression of nitric oxide production. J Nat Med 71:745–756CrossRefPubMed
20.
Zurück zum Zitat Vasconcelos JMJ, Silva AMS, Cavaleiro JAS (1998) Chromones and flavanones from Artemisia campestris subsp. maritima. Phytochemistry 49:1421–1424CrossRef Vasconcelos JMJ, Silva AMS, Cavaleiro JAS (1998) Chromones and flavanones from Artemisia campestris subsp. maritima. Phytochemistry 49:1421–1424CrossRef
21.
Zurück zum Zitat Jeon SH, Chun W, Choi YJ, Kwon YS (2008) Cytotoxic constituents from the bark of Salix hulteni. Arch Pharm Res 31:978–982CrossRefPubMed Jeon SH, Chun W, Choi YJ, Kwon YS (2008) Cytotoxic constituents from the bark of Salix hulteni. Arch Pharm Res 31:978–982CrossRefPubMed
22.
Zurück zum Zitat Kanemaki T, Kitade H, Hiramatsu Y, Kamiyama Y, Okumura T (1993) Stimulation of glycogen degradation by prostaglandin E2 in primary cultured rat hepatocytes. Prostaglandins 45:459–474CrossRefPubMed Kanemaki T, Kitade H, Hiramatsu Y, Kamiyama Y, Okumura T (1993) Stimulation of glycogen degradation by prostaglandin E2 in primary cultured rat hepatocytes. Prostaglandins 45:459–474CrossRefPubMed
24.
Zurück zum Zitat Matsui K, Nishizawa M, Ozaki T, Kimura T, Hashimoto I, Yamada M, Kaibori M, Kamiyama Y, Ito S, Okumura T (2008) Natural antisense transcript stabilizes inducible nitric oxide synthase messenger RNA in rat hepatocytes. Hepatology 47:686–697CrossRefPubMed Matsui K, Nishizawa M, Ozaki T, Kimura T, Hashimoto I, Yamada M, Kaibori M, Kamiyama Y, Ito S, Okumura T (2008) Natural antisense transcript stabilizes inducible nitric oxide synthase messenger RNA in rat hepatocytes. Hepatology 47:686–697CrossRefPubMed
25.
Zurück zum Zitat Sakitani K, Nishizawa M, Inoue K, Masu Y, Okumura T, Ito S (1998) Synergistic regulation of inducible nitric oxide synthase gene by CCAAT/enhancer-binding protein β and nuclear factor-κB in hepatocytes. Genes Cells 3:321–330CrossRefPubMed Sakitani K, Nishizawa M, Inoue K, Masu Y, Okumura T, Ito S (1998) Synergistic regulation of inducible nitric oxide synthase gene by CCAAT/enhancer-binding protein β and nuclear factor-κB in hepatocytes. Genes Cells 3:321–330CrossRefPubMed
26.
Zurück zum Zitat Nishizawa M, Okumura T, Ikeya Y, Kimura T (2012) Regulation of inducible gene expression by natural antisense transcripts. Front Biosci (Landmark Ed.) 17:938–958CrossRef Nishizawa M, Okumura T, Ikeya Y, Kimura T (2012) Regulation of inducible gene expression by natural antisense transcripts. Front Biosci (Landmark Ed.) 17:938–958CrossRef
27.
Zurück zum Zitat Kleinert H, Pautz A, Linker K, Schwarz PM (2004) Regulation of the expression of inducible nitric oxide synthase. Eur J Pharmacol 500:255–266CrossRefPubMed Kleinert H, Pautz A, Linker K, Schwarz PM (2004) Regulation of the expression of inducible nitric oxide synthase. Eur J Pharmacol 500:255–266CrossRefPubMed
28.
Zurück zum Zitat Buss H, Dörrie A, Schmitz ML, Hoffmann E, Resch K, Kracht M (2004) Constitutive and interleukin-1-inducible phosphorylation of p65 NF-κB at serine 536 is mediated by multiple protein kinases including IκB kinase (IKK)-α, IKKβ, IKKε, TRAF family member-associated (TANK)-binding kinase 1 (TBK1), and an unknown kinase and couples p65 to TATA-binding protein-associated factor II31-mediated interleukin-8 transcription. J Biol Chem 279:55633–55643CrossRefPubMed Buss H, Dörrie A, Schmitz ML, Hoffmann E, Resch K, Kracht M (2004) Constitutive and interleukin-1-inducible phosphorylation of p65 NF-κB at serine 536 is mediated by multiple protein kinases including IκB kinase (IKK)-α, IKKβ, IKKε, TRAF family member-associated (TANK)-binding kinase 1 (TBK1), and an unknown kinase and couples p65 to TATA-binding protein-associated factor II31-mediated interleukin-8 transcription. J Biol Chem 279:55633–55643CrossRefPubMed
29.
Zurück zum Zitat Perkins ND (2006) Post-translational modifications regulating the activity and function of the nuclear factor kappa B pathway. Oncogene 25:6717–6730CrossRefPubMed Perkins ND (2006) Post-translational modifications regulating the activity and function of the nuclear factor kappa B pathway. Oncogene 25:6717–6730CrossRefPubMed
30.
Zurück zum Zitat Tsuchihashi R, Kodera M, Sakamoto S, Nakajima Y, Yamazaki T, Niiho Y, Nohara T, Kinjo J (2009) Microbial transformation and bioactivation of isoflavones from Pueraria flowers by human intestinal bacterial strains. J Nat Med 63:254–260CrossRefPubMed Tsuchihashi R, Kodera M, Sakamoto S, Nakajima Y, Yamazaki T, Niiho Y, Nohara T, Kinjo J (2009) Microbial transformation and bioactivation of isoflavones from Pueraria flowers by human intestinal bacterial strains. J Nat Med 63:254–260CrossRefPubMed
31.
Zurück zum Zitat Ververidis F, Trantas E, Douglas C, Vollmer G, Kretzschmar G, Panopoulos N (2007) Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part I: chemical diversity, impacts on plant biology and human health. Biotechnol J 2:1214–1234CrossRefPubMed Ververidis F, Trantas E, Douglas C, Vollmer G, Kretzschmar G, Panopoulos N (2007) Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part I: chemical diversity, impacts on plant biology and human health. Biotechnol J 2:1214–1234CrossRefPubMed
32.
Zurück zum Zitat Nakajima A, Yamamoto Y, Yoshinaka N, Namba M, Matsuo H, Okuyama T, Yoshigai E, Okumura T, Nishizawa M, Ikeya Y (2015) A new flavanone and other flavonoids from green perilla leaf extract inhibit nitric oxide production in interleukin 1β-treated hepatocytes. Biosci Biotechnol Biochem 79:138–146CrossRefPubMed Nakajima A, Yamamoto Y, Yoshinaka N, Namba M, Matsuo H, Okuyama T, Yoshigai E, Okumura T, Nishizawa M, Ikeya Y (2015) A new flavanone and other flavonoids from green perilla leaf extract inhibit nitric oxide production in interleukin 1β-treated hepatocytes. Biosci Biotechnol Biochem 79:138–146CrossRefPubMed
33.
Zurück zum Zitat Bai D, Ueno L, Vogt PK (2009) Akt-mediated regulation of NFκB and the essentialness of NFκB for the oncogenicity of PI3 K and Akt. Int J Cancer 125:2863–2870CrossRefPubMedPubMedCentral Bai D, Ueno L, Vogt PK (2009) Akt-mediated regulation of NFκB and the essentialness of NFκB for the oncogenicity of PI3 K and Akt. Int J Cancer 125:2863–2870CrossRefPubMedPubMedCentral
34.
Zurück zum Zitat Yamanishi R, Yoshigai E, Okuyama T, Mori T, Murase H, Machida T, Okumura T, Nishizawa M (2014) The anti-inflammatory effects of flavanol-rich lychee fruit extract in rat hepatocytes. PLoS One 9:e93818CrossRefPubMedPubMedCentral Yamanishi R, Yoshigai E, Okuyama T, Mori T, Murase H, Machida T, Okumura T, Nishizawa M (2014) The anti-inflammatory effects of flavanol-rich lychee fruit extract in rat hepatocytes. PLoS One 9:e93818CrossRefPubMedPubMedCentral
35.
Zurück zum Zitat Kim KY, Kang H (2016) Sakuranetin inhibits inflammatory enzyme, cytokine, and costimulatory molecule expression in macrophages through modulation of JNK, p38, and STAT1. Evid Based Complement Alternat Med 2016:9824203PubMedPubMedCentral Kim KY, Kang H (2016) Sakuranetin inhibits inflammatory enzyme, cytokine, and costimulatory molecule expression in macrophages through modulation of JNK, p38, and STAT1. Evid Based Complement Alternat Med 2016:9824203PubMedPubMedCentral
36.
Zurück zum Zitat Ye K, Dinarello CA, Clark BD (1993) Identification of the promoter region of human interleukin 1 type I receptor gene: multiple initiation sites, high G + C content, and constitutive expression. Proc Natl Acad Sci USA 90:2295–2299CrossRefPubMed Ye K, Dinarello CA, Clark BD (1993) Identification of the promoter region of human interleukin 1 type I receptor gene: multiple initiation sites, high G + C content, and constitutive expression. Proc Natl Acad Sci USA 90:2295–2299CrossRefPubMed
37.
Zurück zum Zitat Yoshigai E, Hara T, Araki Y, Tanaka Y, Oishi M, Tokuhara K, Kaibori M, Okumura T, Kwon AH, Nishizawa M (2013) Natural antisense transcript-targeted regulation of inducible nitric oxide synthase mRNA levels. Nitric Oxide 30:9–16CrossRefPubMed Yoshigai E, Hara T, Araki Y, Tanaka Y, Oishi M, Tokuhara K, Kaibori M, Okumura T, Kwon AH, Nishizawa M (2013) Natural antisense transcript-targeted regulation of inducible nitric oxide synthase mRNA levels. Nitric Oxide 30:9–16CrossRefPubMed
38.
Zurück zum Zitat Okuyama T, Nakatake R, Kaibori M, Okumura T, Kon M, Nishizawa M (2018) A sense oligonucleotide to inducible nitric oxide synthase mRNA increases the survival rate of rats in septic shock. Nitric Oxide 72:32–40CrossRefPubMed Okuyama T, Nakatake R, Kaibori M, Okumura T, Kon M, Nishizawa M (2018) A sense oligonucleotide to inducible nitric oxide synthase mRNA increases the survival rate of rats in septic shock. Nitric Oxide 72:32–40CrossRefPubMed
Metadaten
Titel
Sakuranetin downregulates inducible nitric oxide synthase expression by affecting interleukin-1 receptor and CCAAT/enhancer-binding protein β
verfasst von
Yuko Yamauchi
Tetsuya Okuyama
Toshinari Ishii
Tadayoshi Okumura
Yukinobu Ikeya
Mikio Nishizawa
Publikationsdatum
01.03.2019
Verlag
Springer Singapore
Erschienen in
Journal of Natural Medicines / Ausgabe 2/2019
Print ISSN: 1340-3443
Elektronische ISSN: 1861-0293
DOI
https://doi.org/10.1007/s11418-018-1267-x

Weitere Artikel der Ausgabe 2/2019

Journal of Natural Medicines 2/2019 Zur Ausgabe