Zingiber officinale Roscoe (Ginger) and its Bioactive Compounds in Diabetes: A Systematic Review of Clinical Studies and Insight of Mechanism of Action


Cite item

Full Text

Abstract

Background:Zingiber officinale Roscoe (Ginger) belongs to the Zingiberaceae family, which is renowned for its rich nutritional and phytochemical composition, and has been validated for its anti-diabetic and anti-inflammatory properties via in vitro, in vivo, and clinical studies. Nonetheless, a comprehensive review of these pharmacological studies, especially clinical studies, together with an analysis of the mechanism of action of the bioactive compounds is still lacking. This review provided a comprehensive and updated analysis of the anti-diabetic efficacy of Z. officinale and its compounds ginger enone, gingerol, paradol, shogaol, and zingerone.

Methods:The present systematic review was conducted using the PRISMA guidelines. Scopus, ScienceDirect, Google Scholar, and PubMed were the main databases used for retrieving information from inception to March 2022.

Results:From the findings obtained, Z. officinale can be regarded as a therapeutic species showing significant improvement in clinical studies on glycemic parameters (Fasting blood glucose (FBG), hemoglobin A1C (HbA1c), and insulin resistance). In addition, the bioactive compounds of Z. officinale act via several mechanisms as revealed by in vitro and in vivo studies. Overall, these mechanisms were by increasing glucose-stimulated insulin secretion, sensitising insulin receptors and raising glucose uptake, translocation of GLUT4, inhibition of advanced glycation end product-induced increase of reactive oxygen species, regulation of hepatic gene expression of enzymes associated with glucose metabolism, regulation of the level of pro-inflammatory cytokines, amelioration of the pathological injuries of kidneys, protective effect on the morphology of β-cells as well as its antioxidant mechanisms, among others.

Conclusion:Z. officinale and its bioactive compounds displayed promising results in in vitro and in vivo systems, nevertheless, it is highly recommended that human trials be conducted on these compounds since clinical studies are the core of medical research and considered the final stages of the drug development process.

About the authors

Bao Van

Institute of Research and Development, Duy Tan University

Email: info@benthamscience.net

Ashraf Abdalla

Department of Pharmacology and Toxicology, College of Pharmacy, Umm Al-Qura University

Author for correspondence.
Email: info@benthamscience.net

Alanood Algarni

Department of Pharmacology and Toxicology, College of Pharmacy, Umm Al-Qura University

Email: info@benthamscience.net

Asaad Khalid

Substance Abuse and Toxicology Research Center, Jazan University

Email: info@benthamscience.net

Gokhan Zengin

Department of Biology, Faculty of Science, Selcuk University

Email: info@benthamscience.net

Muhammad Aumeeruddy

Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius

Email: info@benthamscience.net

Mohamad Mahomoodally

Department of Health Sciences, Faculty of Medicine and Health Sciences,, University of Mauritius

Author for correspondence.
Email: info@benthamscience.net

References

  1. Sun, H.; Saeedi, P.; Karuranga, S.; Pinkepank, M.; Ogurtsova, K.; Duncan, B.B.; Stein, C.; Basit, A.; Chan, J.C.N.; Mbanya, J.C.; Pavkov, M.E.; Ramachandaran, A.; Wild, S.H.; James, S.; Herman, W.H.; Zhang, P.; Bommer, C.; Kuo, S.; Boyko, E.J.; Magliano, D.J. IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045. Diabetes Res. Clin. Pract., 2022, 183, 109119. doi: 10.1016/j.diabres.2021.109119 PMID: 34879977
  2. Althobaiti, F.M.; Alsanosi, S.M.; Falemban, A.H.; Alzahrani, A.R.; Fataha, S.A.; Salih, S.O.; Alrumaih, A.M.; Alotaibi, K.N.; Althobaiti, H.M.; Al-Ghamdi, S.S.; Ayoub, N. Efficacy and safety of empagliflozin in type 2 diabetes mellitus Saudi patients as add-on to antidiabetic therapy: A prospective, open-label, observational study. J. Clin. Med., 2022, 11(16), 4769. doi: 10.3390/jcm11164769 PMID: 36013008
  3. Alkhudhayri, S.; Sajini, R.; Alharbi, B.; Qabbani, J.; Al-Hindi, Y.; Fairaq, A.; Yousef, A. Investigating the beneficial effect of aliskiren in attenuating neuropathic pain in diabetic Sprague-Dawley rats. Endocrinol Diabetes Metab. 2020 Nov 25; 4(2):e00209. doi: 10.1002/edm2.209
  4. Sanlier, N.; Gencer, F. Role of spices in the treatment of diabetes mellitus: A mini review. Trends Food Sci. Technol., 2020, 99, 441-449.
  5. Alharbi, A.; Alduribi, A.; Alghthami, A.; Elnaem, M.; Alsenani, F.S.; Haseeb, A.; Ahmed, N.J.; Elrggal, M. Coping with diabetes during the COVID-19 lockdown in Saudi Arabia: Lessons learned in the post-pandemic Era. Cureus. 2022, 14(11), e31522. doi: 10.7759/cureus.31522
  6. The Plant List. 2013. Available from: http://www.theplantlist.org/1.1/browse/A/Leguminosae/Trigonella/
  7. Mahomoodally, M.; Aumeeruddy, M.Z.; Rengasamy, K.R.R.; Roshan, S.; HammadRoshan, S.; Pandohee, J.; Hu, X.; Zengin, G. Ginger and its active compounds in cancer therapy: From folk uses to nano-therapeutic applications. Semin Cancer Biol, 2021, 69, 140-149.
  8. Bhandari, U.; kanojia, R.; Pillai, K.K. Effect of ethanolic extract of Zingiber officinale on dyslipidaemia in diabetic rats. J. Ethnopharmacol., 2005, 97(2), 227-230. doi: 10.1016/j.jep.2004.11.011 PMID: 15707757
  9. Althaqafi, A.; Ali, M.; Alzahrani, Y.; Ming, L.C.; Hussain, Z. How safe are fluoroquinolones for diabetic patients? a systematic review of dysglycemic and neuropathic effects of fluoroquinolones. Therapeutics and Clinical Risk Management. 2021, 17, 1083-1090. doi: 10.2147/TCRM.S284171
  10. Ojewole, J.A.O. Analgesic, antiinflammatory and hypoglycaemic effects of ethanol extract of Zingiber officinale (roscoe) rhizomes (zingiberaceae) in mice and rats. Phytother. Res., 2006, 20(9), 764-772. doi: 10.1002/ptr.1952 PMID: 16807883
  11. Ali, A.M.; El-Nour, M.E.; Yagi, S.M.; Qahtan, A.A.; Alatar, A.A.; Abdel-Salam, E.M.; Zengin, G. Cytotoxicity, phytochemical screening and genetic analysis of ginger (Zingiber officinale Rosc.) callus and rhizome. S. Afr. J. Bot., 2021.
  12. Azzi, R.; Djaziri, R.; Lahfa, F.; Sekkal, F.Z.; Benmehdi, H.; Belkacem, N. Ethnopharmacological survey of medicinal plants used in the traditional treatment of diabetes mellitus in the North Western and South Western Algeria. J. Med. Plants Res., 2012, 6(10), 2041-2050.
  13. Telli, A.; Esnault, M.A.; Ould El Hadj Khelil, A. An ethnopharmacological survey of plants used in traditional diabetes treatment in south-eastern Algeria (Ouargla province). J. Arid Environ., 2016, 127, 82-92. doi: 10.1016/j.jaridenv.2015.11.005
  14. Kadir, M.F.; Bin Sayeed, M.S.; Shams, T.; Mia, M.M.K. Ethnobotanical survey of medicinal plants used by Bangladeshi traditional health practitioners in the management of diabetes mellitus. J. Ethnopharmacol., 2012, 144(3), 605-611. doi: 10.1016/j.jep.2012.09.050 PMID: 23063956
  15. Lawin, I.; Lalèyè, F.; Agbani, O.; Assogbadjo, A. Ethnobotanical assessment of the plant species used in the treatment of diabetes in the Sudano-Guinean zone of Benin. J. Anim. Plant Sci., 2015, 26(1), 4108-4123.
  16. Özkum, D.; Aki, Ö.; Toklu, H. Herbal medicine use among diabetes mellitus patients in Northern Cyprus. J. Med. Plants Res., 2013, 7, 1652-1664.
  17. Demoz, M.; Gachoki, K.; Mungai, K.; Negusse, B. Ethnobotanical survey and preliminary phytochemical studies of plants traditionally used for diabetes in Eritrea. European J. Med. Plants, 2015, 9(2), 1-11. doi: 10.9734/EJMP/2015/18777
  18. Bading Taika, B.; Bouckandou, M.; Souza, A.; Bourobou Bourobou, H.P.; MacKenzie, L.S.; Lione, L. An overview of anti-diabetic plants used in Gabon: Pharmacology and toxicology. J. Ethnopharmacol., 2018, 216, 203-228. doi: 10.1016/j.jep.2017.12.036 PMID: 29305175
  19. Pieroni, A.; Muenz, H.; Akbulut, M.; Başer, K.H.C.; Durmuşkahya, C. Traditional phytotherapy and trans-cultural pharmacy among Turkish migrants living in Cologne, Germany. J. Ethnopharmacol., 2005, 102(1), 69-88. doi: 10.1016/j.jep.2005.05.018 PMID: 16002248
  20. Diallo, A.; Traore, M.S.; Keita, S.M.; Balde, M.A.; Keita, A.; Camara, M.; Miert, S.V.; Pieters, L.; Balde, A.M. Management of diabetes in Guinean traditional medicine: An ethnobotanical investigation in the coastal lowlands. J. Ethnopharmacol., 2012, 144(2), 353-361. doi: 10.1016/j.jep.2012.09.020 PMID: 23006605
  21. Chhetri, D.R.; Parajuli, P.; Subba, G.C. Antidiabetic plants used by Sikkim and Darjeeling Himalayan tribes, India. J. Ethnopharmacol., 2005, 99(2), 199-202. doi: 10.1016/j.jep.2005.01.058 PMID: 15894127
  22. Mall, T.; Sahani, S. Diversity of ethnomedicinal plants for diabetes from Bahraich (UP) India. Int J Interdiscip Multidiscip Stud, 2013, 1, 13-23.
  23. Aadhan, K.; Anand, S. Survey of medicinal plants used for the treatment of diabetes by the Paliyar’s Tribe in Sadhuragiri hills, Tamil Nadu, India. Int. J. Herb. Med., 2017, 5(3), 17-25.
  24. Silalahi, M. Medicinal plants used by the Batak Toba Tribe in Peadundung Village, North Sumatra, Indonesia. Biodiversitas (Surak.), 2019, 20(2), 510-525. doi: 10.13057/biodiv/d200230
  25. Nasution, B.R.; Aththorick, T.A.; Rahayu, S. IOP Conference Series: Earth and Environmental Science, 2018, Vol. 130, pp. 012038
  26. Salehi Nowbandegani, A.; Kiumarcy, S.; Rahmani, F.; Dokouhaki, M.; Khademian, S.; Zarshenas, M.M.; Faridi, P. Ethnopharmacological knowledge of Shiraz and Fasa in Fars region of Iran for diabetes mellitus. J. Ethnopharmacol., 2015, 172, 281-287. doi: 10.1016/j.jep.2015.06.017 PMID: 26113181
  27. Mati, E.; de Boer, H. Ethnobotany and trade of medicinal plants in the Qaysari market, Kurdish autonomous region, Iraq. J. Ethnopharmacol., 2011, 133(2), 490-510. doi: 10.1016/j.jep.2010.10.023 PMID: 20965241
  28. Ahmed, H.M. Ethnopharmacobotanical study on the medicinal plants used by herbalists in Sulaymaniyah Province, Kurdistan, Iraq. J. Ethnobiol. Ethnomed., 2016, 12(1), 8. doi: 10.1186/s13002-016-0081-3 PMID: 26821541
  29. Skalli, S.; Hassikou, R.; Arahou, M. An ethnobotanical survey of medicinal plants used for diabetes treatment in Rabat, Morocco. Heliyon, 2019, 5(3), e01421. doi: 10.1016/j.heliyon.2019.e01421 PMID: 30976694
  30. Kadiri, M.; Ojewumi, A.W.; Agboola, D.A.; Adekunle, M.F. Ethnobotanical survey of plants used in the management of diabetes mellitus in Abeokuta, Nigeria. J. Drug Deliv. Ther., 2015, 5(3), 13-23. doi: 10.22270/jddt.v5i3.1142
  31. Negbenebor, H.; Shehu, K.; Mairami, F.; Adeiza, Z.; Nura, S.; Fagwalawa, L. Ethno botanical survey of medicinal plants used by Hausa people in the management of diabetes mellitus in Kano metropolis, northern Nigeria. European J. Med. Plants, 2017, 18(2), 1-10. doi: 10.9734/EJMP/2017/28562
  32. Abo, K.A.; Fred-Jaiyesimi, A.A.; Jaiyesimi, A.E.A. Ethnobotanical studies of medicinal plants used in the management of diabetes mellitus in South Western Nigeria. J. Ethnopharmacol., 2008, 115(1), 67-71. doi: 10.1016/j.jep.2007.09.005 PMID: 17950547
  33. Amal, M.F.; Masarrat, M. Ethnobotanical survey of plants used in the treatment of diabetes mellitus in Tabuk region, Saudi Arabia Int. J. Curr. Microbiol. Appl. Sci., 2016, 5(6), 258-270. doi: 10.20546/ijcmas.2016.506.029
  34. Singh, G.; Kapoor, I.P.S.; Singh, P.; de Heluani, C.S.; de Lampasona, M.P.; Catalan, C.A.N. Chemistry, antioxidant and antimicrobial investigations on essential oil and oleoresins of Zingiber officinale. Food Chem. Toxicol., 2008, 46(10), 3295-3302. doi: 10.1016/j.fct.2008.07.017 PMID: 18706468
  35. Murugesan, S.; Venkateswaran, M.R.; Jayabal, S.; Periyasamy, S. Evaluation of the antioxidant and anti-arthritic potential of Zingiber officinale Rosc. by in vitro and in silico analysis. S. Afr. J. Bot., 2020, 130, 45-53. doi: 10.1016/j.sajb.2019.12.019
  36. Talebi, M.; İlgün, S.; Ebrahimi, V.; Talebi, M.; Farkhondeh, T.; Ebrahimi, H.; Samarghandian, S. Zingiber officinale ameliorates Alzheimer’s disease and Cognitive Impairments: Lessons from preclinical studies. Biomed. Pharmacother., 2021, 133, 111088. doi: 10.1016/j.biopha.2020.111088 PMID: 33378982
  37. Jadad, A.R.; Moore, R.A.; Carroll, D.; Jenkinson, C.; Reynolds, D.J.M.; Gavaghan, D.J.; McQuay, H.J. Assessing the quality of reports of randomized clinical trials: Is blinding necessary? Control. Clin. Trials, 1996, 17(1), 1-12. doi: 10.1016/0197-2456(95)00134-4 PMID: 8721797
  38. Saxena, M.; Saxena, J.; Nema, R.; Singh, D.; Gupta, A. Phytochemistry of medicinal plants. J. Pharmacogn. Phytochem., 2016, 1, 168-182.
  39. Nagendra Chari, K.L.; Manasa, D.; Srinivas, P.; Sowbhagya, H.B. Enzyme-assisted extraction of bioactive compounds from ginger (Zingiber officinale Roscoe). Food Chem., 2013, 139(1), 509-514. PMID: 23265518
  40. Swapna Sonale, R.; Kadimi, U.S. Characterization of gingerol analogues in supercritical carbon dioxide (SC CO2) extract of ginger (Zingiber officinale, R.,). J. Food Sci. Technol., 2014, 51(11), 3383-3389. doi: 10.1007/s13197-012-0851-4 PMID: 26396335
  41. Choudhari, S.; Kareppa, B. Identification of bioactive compounds of Zingiber officinale Roscoe rhizomes through gas chromatography and mass spectrometry. Int J Pharm Res Dev, 2013, 5, 16-20.
  42. Ghasemzadeh, A.; Jaafar, H.Z.E.; Rahmat, A. Antioxidant activities, total phenolics and flavonoids content in two varieties of Malaysia young ginger (Zingiber officinale Roscoe). Molecules, 2010, 15(6), 4324-4333. doi: 10.3390/molecules15064324 PMID: 20657444
  43. Hasan, H.A.; Raauf, A.M.R.; Razik, B.; Hassan, B.R. Chemical composition and antimicrobial activity of the crude extracts isolated from Zingiber officinale by different solvents. Pharm. Anal. Acta, 2012, 3(9), 1-5.
  44. Hiserodt, R.D.; Franzblau, S.G.; Rosen, R.T. Isolation of 6-, 8-, and 10-Gingerol from Ginger Rhizome by HPLC and Preliminary Evaluation of Inhibition of Mycobacterium avium and Mycobacterium tuberculosis. J. Agric. Food Chem., 1998, 46(7), 2504-2508. doi: 10.1021/jf970948l
  45. Tohma, H.; Gülçin, İ.; Bursal, E.; Gören, A.C.; Alwasel, S.H.; Köksal, E. Antioxidant activity and phenolic compounds of ginger (Zingiber officinale Rosc.) determined by HPLC-MS/MS. J. Food Meas. Charact., 2017, 11(2), 556-566. doi: 10.1007/s11694-016-9423-z
  46. Jiang, H.; Sólyom, A.M.; Timmermann, B.N.; Gang, D.R. Characterization of gingerol-related compounds in ginger rhizome (Zingiber officinale Rosc.) by high-performance liquid chromatography/electrospray ionization mass spectrometry. Rapid Commun. Mass Spectrom., 2005, 19(20), 2957-2964. doi: 10.1002/rcm.2140 PMID: 16189817
  47. Onyenekwe, P.C.; Hashimoto, S. The composition of the essential oil of dried Nigerian ginger (Zingiber officinale Roscoe). Eur. Food Res. Technol., 1999, 209(6), 407-410. doi: 10.1007/s002170050517
  48. Pino, J.A.; Marbot, R.; Rosado, A.; Batista, A. Chemical composition of the essential oil of Zingiber officinale Roscoe L. from Cuba. J. Essent. Oil Res., 2004, 16(3), 186-188. doi: 10.1080/10412905.2004.9698692
  49. Kumar Sharma, P.; Singh, V.; Ali, M. Chemical composition and antimicrobial activity of fresh rhizome essential oil of Zingiber officinale Roscoe. Pharmacogn. J., 2016, 8(3), 185-190. doi: 10.5530/pj.2016.3.3
  50. Yeh, H.; Chuang, C.; Chen, H.; Wan, C.; Chen, T.; Lin, L. Bioactive components analysis of two various gingers (Zingiber officinale Roscoe) and antioxidant effect of ginger extracts. Lebensm. Wiss. Technol., 2014, 55(1), 329-334. doi: 10.1016/j.lwt.2013.08.003
  51. Salmon, C.N.A.; Bailey-Shaw, Y.A.; Hibbert, S.; Green, C.; Smith, A.M.; Williams, L.A.D. Characterisation of cultivars of Jamaican ginger (Zingiber officinale Roscoe) by HPTLC and HPLC. Food Chem., 2012, 131(4), 1517-1522. doi: 10.1016/j.foodchem.2011.09.115
  52. Song, Z.M.; Zhang, X.J.; Yuan, P.P.; Wang, Y.Z.; Li, M.Q.; Liu, Y.F.; Hu, X.Y.; Miao, J.J.; Fang, H.B.; Feng, W.S. Diarylheptanoid glycosides from Zingiber officinale peel and their anti-apoptotic activity. Fitoterapia, 2022, 157, 105109. doi: 10.1016/j.fitote.2021.105109 PMID: 34954262
  53. Khandouzi, N.; Shidfar, F.; Rajab, A.; Rahideh, T.; Hosseini, P.; Taheri, M.M. The effects of ginger on fasting blood sugar, hemoglobin A1c, apolipoprotein B, apolipoprotein AI and malondialdehyde in type 2 diabetic patients. IJPR, 2015, 14(1), 131. PMID: 25561919
  54. Mozaffari-Khosravi, H.; Talaei, B.; Jalali, B.A.; Najarzadeh, A.; Mozayan, M.R. The effect of ginger powder supplementation on insulin resistance and glycemic indices in patients with type 2 diabetes: A randomized, double-blind, placebo-controlled trial. Complement. Ther. Med., 2014, 22(1), 9-16. doi: 10.1016/j.ctim.2013.12.017 PMID: 24559810
  55. Ebrahimzadeh Attari, V.; Mahluji, S.; Asghari Jafarabadi, M.; Ostadrahimi, A. Effects of supplementation with ginger (Zingiber officinale roscoe) on serum glucose, lipid profile and oxidative stress in obese women: A randomized, placebo-controlled clinical trial. Pharm. Sci., 2015, 21(4), 184-191. doi: 10.15171/PS.2015.35
  56. Arablou, T.; Aryaeian, N.; Valizadeh, M.; Sharifi, F.; Hosseini, A.; Djalali, M. The effect of ginger consumption on glycemic status, lipid profile and some inflammatory markers in patients with type 2 diabetes mellitus. Int. J. Food Sci. Nutr., 2014, 65(4), 515-520. doi: 10.3109/09637486.2014.880671 PMID: 24490949
  57. Makhdoomi Arzati, M.; Mohammadzadeh Honarvar, N.; Saedisomeolia, A.; Anvari, S.; Effatpanah, M.; Makhdoomi Arzati, R.; Yekaninejad, M.S.; Hashemi, R.; Djalali, M. The effects of ginger on fasting blood sugar, hemoglobin A1c, and lipid profiles in patients with type 2 diabetes. Int. J. Endocrinol. Metab., 2017, In Press(In Press), e57927. doi: 10.5812/ijem.57927 PMID: 29344037
  58. Shidfar, F.; Rajab, A.; Rahideh, T.; Khandouzi, N.; Hosseini, S.; Shidfar, S. The effect of ginger (Zingiber officinale) on glycemic markers in patients with type 2 diabetes. J. Complement. Integr. Med., 2015, 12(2), 165-170. doi: 10.1515/jcim-2014-0021 PMID: 25719344
  59. Mahluji, S.; Attari, V.E.; Mobasseri, M.; Payahoo, L.; Ostadrahimi, A.; Golzari, S.E.J. Effects of ginger (Zingiber officinale) on plasma glucose level, HbA1c and insulin sensitivity in type 2 diabetic patients. Int. J. Food Sci. Nutr., 2013, 64(6), 682-686. doi: 10.3109/09637486.2013.775223 PMID: 23496212
  60. Nakanekar, A.; Kohli, K.; Tatke, P. Ayurvedic polyherbal combination (PDBT) for prediabetes: A randomized double blind placebo controlled study. J. Ayurveda Integr. Med., 2019, 10(4), 284-289. doi: 10.1016/j.jaim.2018.05.004 PMID: 30661947
  61. Human Metabolome Database, Version 5.0.. 2022. Available from: https://hmdb.ca/
  62. Chen, J.; Sun, J.; Prinz, R.A.; Li, Y.; Xu, X. Gingerenone A sensitizes the insulin receptor and increases glucose uptake by inhibiting the activity of p70 S6 kinase. Mol. Nutr. Food Res., 2018, 62(23), 1800709. doi: 10.1002/mnfr.201800709 PMID: 30296358
  63. Son, M.J.; Miura, Y.; Yagasaki, K. Mechanisms for antidiabetic effect of gingerol in cultured cells and obese diabetic model mice. Cytotechnology, 2015, 67(4), 641-652. doi: 10.1007/s10616-014-9730-3 PMID: 24794903
  64. Yu, L-Y.; Shi, W-L.; Guo, X.G. Cardio-protective role of gingerol along with prominent anti-diabetic cardiomyopathy action in a streptozotocin-induced diabetes mellitus rat model. Cell J., 2017, 19(3), 469-475. PMID: 28836409
  65. Song, S.; Dang, M.; Kumar, M. Anti-inflammatory and renal protective effect of gingerol in high-fat diet/streptozotocin-induced diabetic rats via inflammatory mechanism. Inflammopharmacology, 2019, 27(6), 1243-1254. doi: 10.1007/s10787-019-00569-6 PMID: 30826930
  66. Ghareib, S.A.; El-Bassossy, H.M.; Elberry, A.A.; Azhar, A.; Watson, M.L.; Banjar, Z.M. 6-Gingerol alleviates exaggerated vasoconstriction in diabetic rat aorta through direct vasodilation and nitric oxide generation. Drug Des. Devel. Ther., 2015, 9, 6019-6026. PMID: 26609223
  67. Almatroodi, S.A.; Alnuqaydan, A.M.; Babiker, A.Y.; Almogbel, M.A.; Khan, A.A.; Husain Rahmani, A. 6-Gingerol, a bioactive compound of ginger attenuates renal damage in streptozotocin-induced diabetic rats by regulating the oxidative stress and inflammation. Pharmaceutics, 2021, 13(3), 317. doi: 10.3390/pharmaceutics13030317 PMID: 33670981
  68. Shao, Y.; Yu, Y.; Li, C.; Yu, J.; Zong, R.; Pei, C. Synergistic effect of quercetin and 6-gingerol treatment in streptozotocin induced type 2 diabetic rats and poloxamer P-407 induced hyperlipidemia. RSC Advances, 2016, 6(15), 12235-12242. doi: 10.1039/C5RA16493A
  69. Sampath, C.; Sang, S.; Ahmedna, M. In vitro and in vivo inhibition of aldose reductase and advanced glycation end products by phloretin, epigallocatechin 3-gallate and 6-gingerol. Biomed. Pharmacother., 2016, 84, 502-513. doi: 10.1016/j.biopha.2016.09.073 PMID: 27685794
  70. Samad, M.B.; Mohsin, M.N.A.B.; Razu, B.A.; Hossain, M.T.; Mahzabeen, S.; Unnoor, N.; Muna, I.A.; Akhter, F.; Kabir, A.U.; Hannan, J.M.A. 6-Gingerol, from Zingiber officinale, potentiates GLP-1 mediated glucose-stimulated insulin secretion pathway in pancreatic β-cells and increases RAB8/RAB10-regulated membrane presentation of GLUT4 transporters in skeletal muscle to improve hyperglycemia in Leprdb/db type 2 diabetic mice. BMC Complement. Altern. Med., 2017, 17(1), 395. doi: 10.1186/s12906-017-1903-0 PMID: 28049463
  71. Li, Y.; Tran, V.; Duke, C.; Roufogalis, B. Gingerols of Zingiber officinale enhance glucose uptake by increasing cell surface GLUT4 in cultured L6 myotubes. Planta Med., 2012, 78(14), 1549-1555. doi: 10.1055/s-0032-1315041 PMID: 22828920
  72. Chakraborty, D.; Mukherjee, A.; Sikdar, S.; Paul, A.; Ghosh, S.; Khuda-Bukhsh, A.R. 6-Gingerol isolated from ginger attenuates sodium arsenite induced oxidative stress and plays a corrective role in improving insulin signaling in mice. Toxicol. Lett., 2012, 210(1), 34-43. doi: 10.1016/j.toxlet.2012.01.002 PMID: 22285432
  73. Lee, J.O.; Kim, N.; Lee, H.J.; Moon, J.W.; Lee, S.K.; Kim, S.J.; Kim, J.K.; Park, S.H.; Kim, H.S. 6-gingerol affects glucose metabolism by dual regulation via the AMPKα2-mediated AS160-Rab5 pathway and AMPK-mediated insulin sensitizing effects. J. Cell. Biochem., 2015, 116(7), 1401-1410. doi: 10.1002/jcb.25100 PMID: 25694332
  74. Kim, H.J.; Kim, I.S.; Rehman, S.U.; Ha, S.K.; Nakamura, K.; Yoo, H.H. Effects of 6-paradol, an unsaturated ketone from gingers, on cytochrome P450-mediated drug metabolism. Bioorg. Med. Chem. Lett., 2017, 27(8), 1826-1830. doi: 10.1016/j.bmcl.2017.02.047 PMID: 28274629
  75. Wei, C.K.; Tsai, Y.H.; Korinek, M.; Hung, P.H.; El-Shazly, M.; Cheng, Y.B.; Wu, Y.C.; Hsieh, T.J.; Chang, F.R. 6-paradol and 6-shogaol, the pungent compounds of ginger, promote glucose utilization in adipocytes and myotubes, and 6-paradol reduces blood glucose in high-fat diet-fed mice. Int. J. Mol. Sci., 2017, 18(1), 168. doi: 10.3390/ijms18010168 PMID: 28106738
  76. Fajrin, F.A.; Rahmayanti, F.; Pratoko, D.K. The binding prediction of 6-paradol and its derivatives on TRPV1 agonist as a new compound for treating painful diabetic neuropathy. Jurnal ILMU DASAR, 2020, 21(2), 133-138. doi: 10.19184/jid.v21i2.15501
  77. Fajrin, F.A.; Nugroho, A.E.; Nurrochmad, A.; Susilowati, R. Ginger extract and its compound, 6-shogaol, attenuates painful diabetic neuropathy in mice via reducing TRPV1 and NMDAR2B expressions in the spinal cord. J. Ethnopharmacol., 2020, 249, 112396. doi: 10.1016/j.jep.2019.112396 PMID: 31743763
  78. Yi, J.K.; Ryoo, Z.Y.; Ha, J.J.; Oh, D.Y.; Kim, M.O.; Kim, S.H. Beneficial effects of 6-shogaol on hyperglycemia, islet morphology and apoptosis in some tissues of streptozotocin-induced diabetic mice. Diabetol. Metab. Syndr., 2019, 11(1), 15. doi: 10.1186/s13098-019-0407-0 PMID: 30805033
  79. Nonaka, K.; Bando, M.; Sakamoto, E.; Inagaki, Y.; Naruishi, K.; Yumoto, H.; Kido, J.I. 6-Shogaol inhibits advanced glycation end-products-induced IL-6 and ICAM-1 expression by regulating oxidative responses in human gingival fibroblasts. Molecules, 2019, 24(20), 3705. doi: 10.3390/molecules24203705 PMID: 31619000
  80. Malakul, W.; Pengnet, S. Inhibitory effect of 6-shogaol on fructose-induced protein glycation and oxidation in vitro. Naresuan Univ J. Sci. Tech., 2017, 25(2), 1-9. NUJST.
  81. Ahmad, B.; Rehman, M.U.; Amin, I.; Mir, M.R.; Ahmad, S.B.; Farooq, A.; Muzamil, S.; Hussain, I.; Masoodi, M.; Fatima, B. Zingerone (4-(4-hydroxy-3-methylphenyl) butan-2-one) protects against alloxan-induced diabetes via alleviation of oxidative stress and inflammation: Probable role of NF-kB activation. Saudi Pharm. J., 2018, 26(8), 1137-1145. doi: 10.1016/j.jsps.2018.07.001 PMID: 30532634
  82. Cui, Y.; Shi, Y.; Bao, Y.; Wang, S.; Hua, Q.; Liu, Y. Zingerone attenuates diabetic nephropathy through inhibition of nicotinamide adenine dinucleotide phosphate oxidase 4. Biomed. Pharmacother., 2018, 99, 422-430. doi: 10.1016/j.biopha.2018.01.051 PMID: 29367111
  83. Rehman, M.U.; Rashid, S.M.; Rasool, S.; Shakeel, S.; Ahmad, B.; Ahmad, S.B.; Madkhali, H.; Ganaie, M.A.; Majid, S.; Bhat, S.A. Zingerone (4-(4-hydroxy-3-methylphenyl)butan-2-one) ameliorates renal function via controlling oxidative burst and inflammation in experimental diabetic nephropathy. Arch. Physiol. Biochem., 2019, 125(3), 201-209. doi: 10.1080/13813455.2018.1448422 PMID: 29537332
  84. Anwer, T.; Alkarbi, Z.A.; Hassan Najmi, A.; Alshahrani, S.; Siddiqui, R.; Khan, G.; Firoz Alam, M. Modulatory effect of zingerone against STZ-nicotinamide induced type-2 diabetes mellitus in rats. Arch. Physiol. Biochem., 2021, 127(4), 304-310. doi: 10.1080/13813455.2019.1637436 PMID: 31389247
  85. Singh, B.; Kumar, A.; Singh, H.; Kaur, S.; Kaur, S.; Singh Buttar, H.; Arora, S.; Singh, B. Zingerone produces antidiabetic effects and attenuates diabetic nephropathy by reducing oxidative stress and overexpression of NF-κB, TNF-α, and COX-2 proteins in rats. J. Funct. Foods, 2020, 74, 104199. doi: 10.1016/j.jff.2020.104199
  86. Jothi, M.A.; Parameswari, C.; Vincent, S. Enhanced glycemic control, pancreas protective, modulated carbohydrate metabolic enzyme activities by zingerone in streptozotocin-induced diabetic rats. World J. Pharm. Res., 2018, 7, 416-435.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2024 Bentham Science Publishers