Open access peer-reviewed chapter

Anti-Inflammatory and Antioxidant Activities of Ginger

Written By

Saja Shareef

Submitted: 18 July 2022 Reviewed: 14 October 2022 Published: 17 November 2022

DOI: 10.5772/intechopen.108611

From the Edited Volume

Ginger - Cultivation and Use

Edited by Prashant Kaushik and Rabia Shabir Ahmad

Chapter metrics overview

144 Chapter Downloads

View Full Metrics

Abstract

Ginger (Zingiber officinale Rosc.), a member of the Zingiberaceae family, is a medicinal herb utilized for its anti-inflammatory and antioxidant qualities. Ginger’s influence on health was discovered due to its high phytochemical content, which includes compounds that eliminate free radicals created by biological systems. Gingerol, shogaol, and other related ginger chemicals limit the body’s production of prostaglandins and leukotrienes. They can also suppress the production of pro-inflammatory cytokines, such as IL-1, TNF-, NF-B, and IL-8. According to our knowledge, NF-B activation is associated with a number of inflammatory disorders, including cancer, kidney injury, and Alzheimer’s disease.

Keywords

  • ginger
  • anti-inflammatory
  • antioxidant
  • shogaol
  • anticancer

1. Introduction

Ginger (Zingiber officinale Rosc.) is a member of the Zingiberaceae family. Ginger is native to Southeast Asia and is used in many nations as a spice and condiment to give flavor to cuisine. In addition, ginger rhizome has been utilized in traditional herbal medicine [1]. The pharmacological potential of ginger is ascribed to its rich phytochemistry [2]. Jolad et al. classify fresh ginger into two broad categories: volatiles and non-volatiles. Sesquiterpene and monoterpenoid hydrocarbons are volatiles that give ginger its distinctive scent and flavor. In contrast, non-volatile pungent chemicals include gingerols, shogaols, paradols, and zingerone [3]. The health advantages of ginger are attributed primarily to its phenolic components, such as gingerols and shogaols. Ginger offers many biological actions, including antioxidant, anti-inflammatory, anticancer, renoprotective impact, antinausea, and antiemetic properties, according to accumulated research.

Advertisement

2. Pharmacological activities of ginger (Zingiber officinale Rosc.)

2.1 Ginger’s antioxidant activity

Overproduction of free radicals, such as reactive oxygen species (ROS), has been shown to play a significant role in the development of numerous chronic diseases [4].

Ginger’s antioxidant activity was assessed in vitro using the ferric-reducing antioxidant power (FRAP), 2,2-diphenyl-1-picrylhydrazyl (DPPH), and 2,2′-azinobis-(3-ethylbenzothiazole-6-sulfonic acid) (ABTS) techniques. The number of phenolic compounds in dried ginger was 5,2 times, 1,1 times, and 2,4 times greater than in fresh, stir-fried, and carbonized ginger, respectively. The antioxidant activity of various gingers tended to exhibit the following characteristics: dried ginger > stir-fried ginger > carbonized ginger > and fresh ginger [5].

Moreover, data from FRAP, oxygen radical absorbance capacity, and cellular antioxidant activity experiments revealed that a polyphenol-rich fraction of the dried ginger powder exhibited strong antioxidant activity [6].

Additionally, the kind of extraction solvent may influence the antioxidant activity of ginger. An ethanolic extract of ginger revealed a significant antioxidant capacity and ferric-reducing ability, whereas an aqueous extract exhibited potent free radical scavenging activity and chelating capacity [6]. In human chondrocyte cells, ginger extract exhibited antioxidant properties, with oxidative stress mediated by interleukin-1 [7]. It increased the production of antioxidant enzymes and decreased the production of reactive oxygen species and lipid peroxidation. Ginger extract lowered the level of malondialdehyde (MDA), which is connected to lipid peroxidation, in stressed rat heart homogenates [8].

Via the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway, ginger and its bioactive components (such as 6-Shogaol) displayed antioxidant action [9]. Nrf2 is a redox-sensitive transcription factor that is mostly expressed in metabolic and detoxifying renal organs and protects against oxidative stress in cells. In addition, ginger phenylpropanoids improved Nrf2 activity and increased the levels of glutathione S-transferase P1 (GSTP1) and the Nrf2 antioxidant response element's downstream effector in foreskin fibroblast cells [10]. In a human mesenchymal stem cell model, the effects of ginger oleoresin on ionizing radiation-induced damage were examined. By translocating Nrf2 to the cell nucleus and stimulating the gene expression of HO-1 and NQO1 (nicotinamide adenine dinucleotide phosphate (NADPH) quinone dehydrogenase 1), oleoresin could reduce the level of reactive oxygen species (ROS). In rats with chlorpyrifos-induced oxidative damage, the 6-gingerol-rich fraction from ginger reduced H2O2 and MDA levels, enhanced antioxidant enzyme activity, and increased glutathione [11].

In addition, ginger extract treatment increased serum levels of antioxidants and testosterone and protected rat testes from cyclophosphamide-induced damage.

2.2 Ginger’s anti-inflammatory activity

Several studies have demonstrated that ginger and its active ingredients exhibit anti-inflammatory properties that may protect against inflammation-related disorders [12]. Phoshatidylinositol-3-kinase (PI3K), protein kinase B (Akt), and nuclear factor kappa light chain-enhancer of activated B cells (NF-B) were primarily responsible for the anti-inflammatory effects. In human intestinal cell models, 6-Shogaol also showed protective properties against tumor necrosis factor (TNF-)-induced intestinal barrier disruption. It also blocked the overexpression of Claudin-2 and the disassembly of Claudin-1 by inhibiting the PI3K/Akt and NF-B signaling pathways [13]. Moreover, a 6-gingerol-rich fraction reduced an increase in inflammatory markers such as myeloperoxidase, NO, and TNF- in the brain, ovaries, and uterus of chlorpyrifos-treated rats [11].

2.3 Renoprotective effect of ginger

Many studies revealed the effect of ginger on kidney dysfunction. From these studies, it was found ginger significantly protects the renal cells and reduces the severity of tubular damage caused by gentamicin. Ginger was effective as a prophylaxis agent, but it has no curative activity [14]. Interestingly the presence of polyphenols and flavonoids in the Z. officinale extract might be responsible for the antioxidant and nephroprotective activities [15]. Furthermore, it was found that injecting ginger (200 mg/kg) in rats induces a considerable decrease in the concentration of urea and creatinine in rat model, improved, restored, and recovered the affected kidney tissue after inducing kidney injury by azathioprine [16].

2.4 Ginger’s kidney protective effect

Numerous research has demonstrated ginger’s efficacy on renal impairment. Ginger greatly protects renal cells and lowers the severity of tubular damage produced by gentamicin, according to these investigations. Ginger was useful as a preventative, but it lacks curative properties [14]. Intriguingly, the antioxidant and nephroprotective properties of the Z. officinale extract may be due to the presence of polyphenols and flavonoids [15]. Moreover, it was discovered that 200 mg/kg of ginger generates a significant drop in the levels of urea and creatinine in rat models, and improves, restores, and recovers damaged kidney tissue induced by azathioprine [16].

2.5 Ginger’s anticancer effect

The method by which ginger acts as a cytotoxin against cancer cells is still a matter of debate among scientists. Ginger contains anti-inflammatory and anti-tumorigenic substances, including [6]-gingerol, [6]-shogaol, [6]-paradol, and zerumbone. Ginger and its bioactive compounds inhibit the progression of colorectal, gastric, ovarian, liver, skin, breast, and prostate cancers [17].

2.6 Ginger’s antiemetic effect

Ginger (and its compounds) exert its antiemetic effects peripherally, within the gastrointestinal system, by boosting gastric tone and motility via anticholinergic and antiserotonergic activities [18]. Additionally, it is said to enhance gastric emptying. This combination of roles explains ginger’s well-known capacity to alleviate symptoms of functional gastrointestinal diseases, such as dyspepsia, abdominal pain, and nausea, which are frequently associated with impaired gastric motility. Three recent studies have explored the effect of ginger on serotonin (5-hydroxytryptamine, 5-HT3, and 5-HT4) and cholinergic (M3) receptor activity; however, the precise mechanism of action of ginger concerning its antiemetic qualities is yet unknown [19].

2.7 Ginger’s effect on liver

In a mouse model, dried ginger (Zingiber officinale) suppresses inflammation, improves pathological alterations, and lowers INF and IL6 levels. It may potentially cause liver damage. NF-B activation is inhibited to reduce proinflammatory responses, TNF, IL-6, and other inflammatory cytokines levels [20].

2.8 Ginger’s effect on diabetes

The consumption of ginger has an impact on lipid profiles, insulin sensitivity, glycemic status, and other metabolic abnormalities in people with type 2 diabetes mellitus (T2DM). Reducing inflammatory substances, such as CRP, IL6, TNF, and others, improves them [21].

It reveals an antagonistic effect against serotonin receptors. Notably, it decreases intestine glucosidase and amylase activity, which reduces glucose absorption [22]. Ginger’s neuroprotective effects on the brains of streptozotocin-induced diabetic rats may also result from changes in astrocyte function. Damage response, decreasing the expression of acetylcholinesterase (AchE), and improving the construction of neurons [23].

2.9 Ginger effect on neurological degenerative diseases

Ginger’s active component, 6-Shogaol, reduces neuroinflammation and cognitive impairments in animal dementia models. Therefore, it plays a significant role in the amelioration of symptoms in Alzheimer’s and other neurological illness patients. It enhances memory in animal models of dementia by suppressing the activity of glial cells and by minimizing memory corruption [24].

In addition, ginger inhibits NF-B,16,17 iNOS, and cyclooxygenase2 activity (COX2) [25]. It protects C57BL/6 mice from inflammation caused by ultraviolet B [26]. Ginger has an inhibitory effect on melanogenesis in B16F10 melanoma cells and can therefore prevent the darkening of the skin (Figure 1) [27].

Figure 1.

Multiple health benefits of ginger [28].

Advertisement

3. Conclusion

Ginger’s pharmacological effects are generally known. Anti-oxidant and anti-inflammatory responses allow it to cure a wide variety of disorders. Ginger’s anticancer effect is well-documented, and its functional components, gingerols, shogaol, and paradols, are useful chemicals that can prevent various malignancies, metastasis, and prevention of cell-cycle development. Additionally, it enhances the condition of the kidneys and digestive tract.

References

  1. 1. Mashadi NS, Ghiasvand R, Mofid MR. Anti-oxidative and anti-inflammatory effects of ginger in health and physical activity: Review of current evidence. International Journal of Preventive Medicine. 2013;4(1):36-42
  2. 2. Stoner GD. Ginger: Is it ready for prime time? Cancer Prevention Research. 2013;6(4):257-262
  3. 3. Jolad SD, Lantz RC, Solyom AM, Chen GJ, Bates RB, Timmermann BN. Fresh organically grown ginger (Zingiber officinale): Composition and effects on LPS-induced PGE2 production. Phytochemistry. 2004;65(13):1937-1954
  4. 4. Poprac P, Jomova K, Simunkova M, Kollar V, Rhodes CJ, Valko M. Targeting free radicals in oxidative stress-related human diseases. Trends in Pharmacological Sciences. 2017;38(7):592-607
  5. 5. Li Y, Hong Y, Han Y, Wang Y, Xia L. Chemical characterization and antioxidant activities comparison in fresh, dried, stir-frying and carbonized ginger. Journal of Chromatography, B: Analytical Technologies in the Biomedical and Life Sciences. 2016;1011:223-232
  6. 6. Sakulnarmrat K, Srzednicki G, Konczak I. Antioxidant, enzyme inhibitory and antiproliferative activity of polyphenolic-rich fraction of commercial dry ginger powder. International Journal of Food Science and Technology. 2015;50(10):2229-2235
  7. 7. Hosseinzadeh A, Bahrampour Juybari K, Fatemi MJ, Kamarul T, Bagheri A, Tekiyehmaroof N, et al. Protective effect of ginger (Zingiber officinale Roscoe) extract against oxidative stress and mitochondrial apoptosis induced by interleukin-1β in cultured chondrocytes. Cells, Tissues, Organs. 2017;204(5-6):241-250
  8. 8. Ludis M, Carolina RA, Milena FA, Adriana G. Effect of ginger extract on membrane potential changes and AKT activation on a peroxide-induced oxidative stress cell model. Free Radical Biology & Medicine. 2018;120:S49
  9. 9. Peng S, Yao J, Liu Y, Duan D, Zhang X, Fang J. Activation of Nrf2 target enzymes conferring protection against oxidative stress in PC12 cells by ginger principal constituent 6-shogaol. Food & Function. 2015;6(8):2813-2823
  10. 10. Ji K, Fang L, Zhao H, Li Q , Shi Y, Xu C, et al. Ginger oleoresin alleviated γ-ray irradiation-induced reactive oxygen species via the Nrf2 protective response in human mesenchymal stem cells. Oxidative Medicine and Cellular Longevity. 2017;2017
  11. 11. Abolaji AO, Ojo M, Afolabi TT, Arowoogun MD, Nwawolor D, Farombi EO. Protective properties of 6-gingerol-rich fraction from Zingiber officinale (Ginger) on chlorpyrifos-induced oxidative damage and inflammation in the brain, ovary and uterus of rats. Chemico-Biological Interactions. 2017;270:15-23
  12. 12. Ezzat SM, Ezzat MI, Okba MM, Menze ET, Abdel-Naim AB. The hidden mechanism beyond ginger (Zingiber officinale Rosc.) potent in vivo and in vitro anti-inflammatory activity. Journal of Ethnopharmacology. 2018;214:113-123
  13. 13. Luettig J, Rosenthal R, Lee IFM, Krug SM, Schulzke JD. The ginger component 6-shogaol prevents TNF-α-induced barrier loss via inhibition of PI3K/Akt and NF-κB signaling. Molecular Nutrition & Food Research. 2016;60(12):2576-2586
  14. 14. Nasri H, Nematbakhsh M, Ghobadi S, Ansari R, Shahinfard N, Rafieian-Kopaei M. Preventive and curative effects of ginger extract against histopathologic changes of gentamicin-induced tubular toxicity in rats. International Journal of Preventive Medicine. 2013;4(3):316-321
  15. 15. Shan B, Cai YZ, Sun M, Corke H. Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. Journal of Agricultural and Food Chemistry. 2005;53(20):7749-7759
  16. 16. Shareef SM, Khaleel RA, Hameed ZE, Alsaraf KM. The protective effect of zingiber officinale l. Extract on kidney tissues and blood factors of kidney functions after the damage caused by azathioprine. Science Pharmaceutical. 2021;32(4):78-86
  17. 17. Hung JYU, Hsu YAL, Li C Te, Ko YC, Ni WC, Huang MS, et al. 6-shogaol, an active constituent of dietary ginger, induces autophagy by inhibiting the AKT/mTOR pathway in human non-small cell lung cancer A549 cells. Journal of Agricultural and Food Chemistry 2009;57(20):9809-9816.
  18. 18. Abdel-Aziz H, Windeck T, Ploch M, Verspohl EJ. Mode of action of gingerols and shogaols on 5-HT3 receptors: Binding studies, cation uptake by the receptor channel and contraction of isolated guinea-pig ileum. European Journal of Pharmacology. 2006;530(1-2):136-143
  19. 19. Walstab J, Krüger D, Stark T, Hofmann T, Demir IE, Ceyhan GO, et al. Ginger and its pungent constituents non-competitively inhibit activation of human recombinant and native 5-HT3 receptors of enteric neurons. Neurogastroenterology and Motility. 2013;25(5):439-448
  20. 20. Li XH, McGrath KC, Nammi S, Heather AK, Roufogalis BD. Attenuation of liver pro-inflammatory responses by Zingiber officinale via inhibition of NF-kappa B activation in high-fat diet-fed rats. Basic & Clinical Pharmacology & Toxicology. 2012;110(3):238-244
  21. 21. Mahluji S, Ostadrahimi A, Mobasseri M, Attari VE, Payahoo L. Anti-inflammatory effects of zingiber officinale in type 2 diabetic patients. Advanced Pharmaceutical Bulletin. 2013;3(2):273
  22. 22. Goyal RK, Kadnur SV. Beneficial effects of Zingiber officinale on goldthioglucose induced obesity. Fitoterapia. 2006;77(3):160-163
  23. 23. El-Akabawy G, El-Kholy W. Neuroprotective effect of Ginger in the brain of streptozotocin-induced diabetic rats. Annals of Anatomy-Anatomischer Anzeiger. 2014;196(2):119-128
  24. 24. Moon M, Kim HG, Choi JG, et al. 6-Shogaol, an active constituent of Ginger, attenuates neuroinflammation and cognitive deficits in animal models of dementia. Biochemical and Biophysical Research Communications. 2014;449(1):8-13
  25. 25. Shim S, Kim S, Choi D-S, Kwon Y-B, Kwon J. Anti-inflammatory effects of [6]-shogaol: Potential roles of HDAC inhibition and HSP70 induction. Food and Chemical Toxicology. 2011;49(11):2734-2740
  26. 26. Guahk G-H, Ha SK, Jung H-S, et al. Zingiber officinale protects HaCaT cells and C57BL/6 mice from ultraviolet B-induced inflammation. Journal of Medicinal Food. 2010;13(3):673-680
  27. 27. Huang H-C, Chiu S-H, Chang T-M. Inhibitory effect of [6]-Gingerol on melanogenesis in B16F10 melanoma cells and a possible mechanism of action. Bioscience, Biotechnology, and Biochemistry. 2011;75(6):1067-1072
  28. 28. Srinivasan K. Ginger rhizomes (Zingiber officinale): A spice with multiple health beneficial potentials. PharmaNutrition. 2017;5(1):18-28

Written By

Saja Shareef

Submitted: 18 July 2022 Reviewed: 14 October 2022 Published: 17 November 2022