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Review

Therapeutic Potential and Recent Advances of Curcumin in the Treatment of Aging-Associated Diseases

by
Sathish Sundar Dhilip Kumar
,
Nicolette Nadene Houreld
and
Heidi Abrahamse
*
Laser Research Centre, Faculty of Health Sciences, University of Johannesburg, Johannesburg-2028, South Africa
*
Author to whom correspondence should be addressed.
Molecules 2018, 23(4), 835; https://doi.org/10.3390/molecules23040835
Submission received: 16 March 2018 / Revised: 29 March 2018 / Accepted: 30 March 2018 / Published: 5 April 2018
(This article belongs to the Special Issue Plant Derived Natural Products and Age Related Diseases)

Abstract

:
Curcumin, a low molecular weight, lipophilic, major yellow natural polyphenolic, and the most well-known plant-derived compound, is extracted from the rhizomes of the turmeric (Curcuma longa) plant. Curcumin has been demonstrated as an effective therapeutic agent in traditional medicine for the treatment and prevention of different diseases. It has also shown a wide range of biological and pharmacological effects in drug delivery, and has actively been used for the treatment of aging-associated diseases, including cardiovascular diseases, atherosclerosis, neurodegenerative diseases, cancer, rheumatoid arthritis, ocular diseases, osteoporosis, diabetes, hypertension, chronic kidney diseases, chronic inflammation and infection. The functional application and therapeutic potential of curcumin in the treatment of aging-associated diseases is well documented in the literature. This review article focuses mainly on the potential role of plant-derived natural compounds such as curcumin, their mechanism of action and recent advances in the treatment of aging-associated diseases. Moreover, the review briefly recaps on the recent progress made in the preparation of nanocurcumins and their therapeutic potential in clinical research for the treatment of aging-associated diseases.

1. Introduction

Aging is an inevitable process for all organisms. It creates numerous cellular and molecular malfunctions which lead to the development of various chronic diseases, also generally referred to as aging-associated diseases. The occurrence of aging-associated diseases is increasing worldwide and becoming the leading causes of disability and increased risk of mortality [1,2,3]. Some of the most common aging-associated diseases are atherosclerosis, cancer, cardiovascular diseases, chronic inflammation, chronic kidney diseases, diabetes, neurodegenerative diseases, hypertension, rheumatoid arthritis, ocular diseases, osteoporosis, and infections [4,5]. Aging-associated diseases usually develop in middle age after the prolonged exposure to an unhealthy early-life environment involving the excessive usage of tobacco and alcohol, anxiety, lack of physical activity and the consumption of a high-fat diet [1]. Clinical trials and epidemiological data has suggested that healthy lifestyle interventions help to prevent many aging-associated chronic diseases, and many can even be reversed [6].
Plant-derived natural products play a vital role in the prevention and treatment of aging-associated diseases [7]. Natural products extracted from plants has been used as an active ingredient in traditional medicine for many centuries [8]. Some plant-derived natural products possess a wide range of biological and pharmacological properties that have become indispensable in modern pharmacotherapy, e.g., paclitaxel (an anticancer drug) from Taxus brevifolia, vincristine and vinblastine (anticancer drugs) from Catharanthus roseus, camptothecin (anticancer drug) from Camptotheca acuminata and quercetin (anticancer drug), a polyphenol found in various vegetables and fruits [9,10,11]. Curcumin, which has the chemical structure 1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione, is a natural yellow, polyphenolic pigment compound extracted from the rhizomes of turmeric (Curcuma longa), is among these plant-derived natural products [12,13]. It is used as a food ingredient in all forms of Indian cuisine, and it shows a wide range of pharmacological activities. It is used for the treatment of neurodegenerative [14], atherosclerosis [15], cardiovascular [16], cancer [17], pulmonary, autoimmune and neoplastic diseases [18], biliary and hepatic disorders [19], diabetes [20], wound healing [21], rheumatoid arthritis [22], chronic inflammation [23], chronic kidney diseases [24], hypertension [25], ocular diseases [26], osteoporosis [27], and skin diseases [28]. Although curcumin possesses good therapeutic efficacy in the treatment of different diseases, the clinical administration of curcumin is difficult due to its poor oral bioavailability, low solubility in aqueous solution, and degradation under physiological conditions [13].
Nanocarrier-mediated delivery aids in overcoming the problems associated with curcumin and facilitates successful delivery without affecting its therapeutic efficacy. Several carrier molecules are used to enhance the bioavailability of curcumin such as polymeric nanoparticles (natural and synthetic polymers), liposomes, dendrimers, solid lipid nanoparticles, and gold nanoparticles [29]. Recent research has suggested that nanoformulated curcumin has a better therapeutic index than the native form of curcumin [30]. In this review article we primarily emphasize the therapeutic potential of curcumin and the possible advantages of using nanocurcumin, which possesses higher stability and increased bioavailability than free curcumin, in the prevention and treatment of aging-associated diseases.

2. Curcumin

Turmeric, the golden spice also known as “Indian saffron” is used as a traditional medicine in Southeast Asia [31]. The most important bioactive chemical constituents of turmeric are curcuminoids, which include curcumin, demethoxycurcumin and bisdemethoxycurcumin [32]. Curcumin, a hydrophobic polyphenol, is extracted from the rhizome of the herb Curcuma longa, which belongs to the Zingiberaceae family [33]. It has a wide spectrum of biological and pharmacological activities [34]. Curcumin is less soluble in water and highly soluble in organic solvents including methanol, ethanol, acetone and dimethyl sulfoxide [35]. Curcumin is commonly called diferuloylmethane, and it gives a yellow color to turmeric powder. The chemical structure is shown in Figure 1a. The ultraviolet-visible surface plasmon resonance spectrum of curcumin exhibits a strong absorption peak between 420–430 nm. In the last 10 years, over 15,000 scientific papers have been published on curcumin, and these numbers have been increasing annually. Scopus results for the period 2008–2017 are shown in Figure 1b.
An extensive literature survey was conducted over the last 10 years on aging-associated diseases and their treatment strategies using the drug curcumin. Atherosclerosis-curcumin, cancer-curcumin, cardiovascular diseases-curcumin, chronic inflammation-curcumin, chronic kidney diseases-curcumin, diabetes-curcumin, hypertension-curcumin, neurodegenerative diseases-curcumin, ocular diseases-curcumin, osteoporosis-curcumin, and rheumatoid arthritis-curcumin were used as keywords to search the “Scopus” database for the period 2008–2017, and the results are represented in Figure 2. The literature study describes the annual publication history and the recent research progress of curcumin in relation to the above-mentioned aging-associated diseases.

Biological and Pharmacological Properties of Curcumin

Currently, curcumin is being investigated as an active therapeutic agent for several types of diseases including cardiovascular, pulmonary, skin disorders, liver disorders, fatigue, neuropathic pain, bone and muscle loss, and anxiety, due to its well reported biological activities which include anti-inflammatory, anti-proliferative, anti-angiogenic, pro-apoptotic, anti-oxidant, wound healing, anti-cancer, anti-viral, and anti-diabetic effects [36,37,38]. It is a well-recognized plant-based drug for the treatment of most chronic diseases. Curcumin has exhibited excellent anti-bacterial activity against both methicillin resistant and sensitive Staphylococcus aureus [39]. It is also one of the most frequently prescribed drugs for the treatment of different skin diseases and skin cancer [28].
Extensive investigation has indicated that curcumin resulted in a reduction in total cholesterol and low-density lipoprotein (LDL) levels in patients suffering from acute coronary syndrome [40], and that it effectively reduced platelet aggregation and hyperlipidemia [41]. Curcumin possesses anti-thrombotic activities and daily consumption helps to maintain anticoagulant status [42]. It can promote cardiac repair and restore cardiac dysfunction [43], molecular understanding in diabetic nephropathy [44], modulate cell cycle regulatory proteins in central nervous system-related disorders including multiple sclerosis [45], and it can be potentially used for the treatment of hepatic diseases [46], and different types of cancers [47]. The beneficial effects of curcumin have also been studied in detail in ocular diseases, which include corneal diseases, eye dryness, conjunctivitis, anterior uveitis, pterygium, regulating calcium hemostasis, cataracts and glaucoma [48].
Various in vitro and in vivo preclinical studies have demonstrated that curcumin has effective biological pharmacological and potential clinical applications by interacting with numerous cellular and molecular targets via a diverse range of mechanisms of action [49], which are presented in Table 1.

3. Therapeutic Potential of Curcumin in Aging-Associated Diseases

The aging process is related to a wide range of disorders. Aging-associated diseases are threatening the elderly population worldwide. Research over the last few decades has studied the therapeutic potential of curcumin and showed the beneficial aspects of curcumin in the prevention and treatment of aging-associated diseases. The therapeutic potential of curcumin used in the treatment of aging-associated diseases is discussed in Table 2.

4. Recent Advances of Nanocurcumin in Aging-Associated Diseases

In recent years, nanotechnology-based drug delivery systems have received considerable attention in drug delivery and pharmaceutical research due to their capability to deliver drugs and other substances (such as targeting ligands, fluorescent dyes) to the targeted region. Nanoformulation offers distinct advantages in drug delivery which include lack of toxicity, high drug loading capacity, controlled drug release, extended shelf life period, higher stability, functionalization with specific targets, intracellular release and targeted delivery [62]. Various nano-based formulations are successfully studied for imaging, diagnostic and therapeutic applications [63]. Recent advances in nanotechnology have facilitated the formulation of nanocurcumin and it significantly improved the therapeutic efficacy and bioavailability of its native counterpart [64] and provides the opportunity for disease specific targeting [65].
Curcumin-loaded spherical polymeric nanoconstructs with lipid chains was assessed in vitro using RAW 264.7 cells. The nanoconstructs significantly modulated the production of pro-inflammatory cytokines without any cytotoxic effect [66]. Curcumin-conjugated magnetic nanoparticles bind with amyloid plaques in mouse brains, which was confirmed through immunohistochemical studies and magnetic resonance images. This study revealed the potential application of curcumin magnetic nanoparticles to visualize amyloid plaques in Alzheimer’s disease [67]. Curcumin loaded zinc oxide nanoparticles encapsulated with a co-polymer were successfully synthesized, and their anticancer activity showed excellent cytotoxicity effects in AGS gastric cancer cells [68]. In vitro and in vivo studies showed that curcumin encapsulated PLGA nanoparticles showed effective targeting and growth inhibition of prostate cancer cells [69]. Meena et al. synthesized small positively charged curcumin nanoparticles using PLGA as a carrier, and tested these nanoparticles in triple-negative breast cancer cells. Nanocurcumin showed higher cellular incorporation and produced more cytotoxic effects than free curcumin, and further apoptosis induction occurred due to DNA damage [70]. Fan et al. fabricated curcumin loaded nanoparticles using bovine serum albumin and dextran as a carrier molecule, and showed improved cellular antioxidant activity in Caco-2 cells [71]. Curcumin loaded solid lipid nanoparticles were synthesized and were revealed as a safe and effective therapeutic agent for the treatment of lipopolysaccharide-induced sepsis in IL-1b transgenic mice [72]. Curcumin nanoparticles possessed cardio protection against palmitate induced cardiomyocyte apoptosis in H9C2 embryonic rat heart-derived cells, and may be an alternative treatment for lipid toxicity and myocardial injury [73]. Dewangan et al. prepared curcumin-carboxymethyl cellulose acetate butyrate nanoparticles in the size range of 166.5 ± 4.2 nm with higher loading efficiency. This study demonstrated superior anti-inflammatory effects without any specific side effects for the successful treatment on adjuvant induced arthritis in rats [74]. The curcumin encapsulated PLGA nanoparticle approach enhanced the effect of curcumin against bone loss. It showed significant beneficial effects on osteoporotic bone loss treatment with an improved therapeutic index [75]. Curcumin encapsulation was performed using a novel nanomicelle formulation which significantly improved in vitro cellular uptake and in vivo corneal permeation as compared to free curcumin [76]. Some to the recent advances in the preparation of nanocurcumin for the treatment of aging-associated diseases are well studied and are listed in Table 3.

5. Clinical Application of Curcumin in Aging-Associated Diseases

Curcumin has been extensively used in clinical trials and is showing positive outcomes for the treatment of aging-associated diseases. The global market is predominantly focused on curcumin as a health supplement due to its effective antioxidant and anti-inflammatory properties [39]. The different aging-associated diseases along with curcumin were used as a keyword to search the “https://clinicaltrials.gov” database. The number of clinical trials are listed in Table 4 and some of the major global clinical trial status of curcumin in aging-associated diseases are listed in Table 5.

6. Future Perspectives and Conclusions

In this review, we discussed in some detail the therapeutic potential of curcumin for the prevention and treatment of aging-associated diseases. Curcumin is a well-known plant-derived compound that exhibits a wide range of biological and pharmacological effects in modern medicine. It is well documented in the literature and shows positive effects on the treatment of aging-associated diseases. However, despite the fact that the native form of curcumin possesses good therapeutic efficacy, the clinical administration is problematic due to their poor oral bioavailability and stability. Recent advances in nanotechnology have helped to overcome these difficulties and efficiently deliver curcumin to the targeted region thereby improving curcumin bioavailability. An extensive literature study strongly suggests that the nanocarrier-mediated delivery of curcumin will become a successful treatment strategy for aging-associated diseases. Moreover, future perspectives should include additional clinical trial investigations on the formulation of nanocurcumin with improved stability and oral bioavailability, and focus more on targeted drug delivery of curcumin for the treatment of aging-associated diseases.

Acknowledgments

Sathish Sundar Dhilip Kumar is supported by funding from the Claude Leon Foundation, South Africa. This work is based on the research supported by the South African Research Chairs Initiative of the Department of Science and Technology and National Research Foundation of South Africa (Grant No. 98337), as well as grants received from the University of Johannesburg (URC), the National Research Foundation (NRF), and the CSIR (Council for Scientific and industrial Research)—NLC (National Laser Centre) Laser Rental Pool Programme.

Author Contributions

S.S.D.K. conceptualized the idea and prepared the review article. N.N.H. was involved in drafting the manuscript, revising it critically for intellectual content, provided professional guidance and is the supervisor of lead author. H.A. organized this study, supplied editorial input and is a co-supervisor of the lead author. All authors read and approved the final manuscript.

Conflicts of Interest

The authors confirm that this article content has no conflict of interest.

References

  1. Prasad, S.; Sung, B.; Aggarwal, B.B. Age-associated chronic diseases requires age-old medicine: Role of chronic inflammation. Prev. Med. 2012, 54, S29–S37. [Google Scholar] [CrossRef] [PubMed]
  2. Tarry-Adkins, J.L.; Ozanne, S.E. Nutrition in early life and age-associated diseases. Ageing Res. Rev. 2017, 39, 96–105. [Google Scholar] [CrossRef] [PubMed]
  3. Ahmad, A.; Banerjee, S.; Wang, Z.; Kong, D.; Majumdar, A.P.N.; Sarkar, F.H. Aging and Inflammation: Etiological culprits of cancer. Curr. Aging Sci. 2009, 2, 174–186. [Google Scholar] [CrossRef] [PubMed]
  4. Tosato, M.; Zamboni, V.; Ferrini, A.; Cesari, M. The aging process and potential interventions to extend life expectancy. Clin. Interv. Aging 2007, 2, 401–412. [Google Scholar] [PubMed]
  5. Kithas, P.A.; Supiano, M.A. Hypertension and chronic kidney disease in the elderly. Adv. Chronic Kidney Dis. 2010, 17, 341–347. [Google Scholar] [CrossRef] [PubMed]
  6. Fontana, L. Modulating Human Aging and Age-Associated Diseases. Biochim. Biophys. Acta 2009, 1790, 1133–1138. [Google Scholar] [CrossRef] [PubMed]
  7. Szymanska, R.; Pospisil, P.; Kruk, J. Plant-derived antioxidants in disease prevention. Oxid. Med. Cell Longev. 2016. [Google Scholar] [CrossRef] [PubMed]
  8. Dias, D.A.; Urban, S.; Roessner, U. A historical overview of natural products in drug discovery. Metabolites 2012, 2, 303–336. [Google Scholar] [CrossRef] [PubMed]
  9. Atanasov, A.G.; Waltenberger, B.; Pferschy-Wenzig, E.-M.; Linder, T.; Wawrosch, C.; Uhrin, P.; Temml, V.; Wang, L.; Schwaiger, S.; Heiss, E.H.; et al. Discovery and resupply of pharmacologically active plant-derived natural products: A review. Biotechnol. Adv. 2015, 33, 1582–1614. [Google Scholar] [CrossRef] [PubMed]
  10. Khan, F.; Niaz, K.; Maqbool, F.; Hassan, F.I.; Abdollahi, M.; Venkata, K.C.N.; Nabavi, S.M.; Bishayee, A. Molecular targets underlying the anticancer effects of quercetin: An update. Nutrients 2016. [Google Scholar] [CrossRef] [PubMed]
  11. Lozano-Perez, A.A.; Rivero, H.C.; Hernandez, M.C.P.; Pagan, A.; Montalban, M.G.; Villora, G.; Cenis, J.L. Silk fibroin nanoparticles: Efficient vehicles for the natural antioxidant quercetin. Int. J. Pharm. 2017, 518, 11–19. [Google Scholar] [CrossRef] [PubMed]
  12. Kumar, S.S.; Surianarayanan, M.; Vijayaraghavan, R.; Mandal, A.B.; MacFarlane, D.R. Curcumin loaded poly(2-hydroxyethyl methacrylate) nanoparticles from gelled ionic liquid–In vitro cytotoxicity and anti-cancer activity in SKOV-3 cells. Eur. J. Pharm. Sci. 2014, 51, 34–44. [Google Scholar] [CrossRef] [PubMed]
  13. Kumar, S.S.; Mahesh, A.; Mahadevan, S.; Mandal, A.B. Synthesis and characterization of curcumin loaded polymer/lipid based nanoparticles and evaluation of their antitumor effects on MCF-7 cells. Biochim. Biophys. Acta 2014, 1840, 1913–1922. [Google Scholar] [CrossRef] [PubMed]
  14. Monroy, A.; Lithgow, G.J.; Alavez, S. Curcumin and neurodegenerative diseases. Biofactors 2013, 39, 122–132. [Google Scholar] [CrossRef] [PubMed]
  15. Olszanecki, R.; Jawien, J.; Gajda, M.; Mateuszuk, L.; Gebska, A.; Korabiowska, M.; Chlopicki, S.; Korbut, R. Effect of curcumin on atherosclerosis in apoE/LDLR-double knockout mice. J. Physiol. Pharmacol. 2005, 56, 627–635. [Google Scholar] [PubMed]
  16. Wongcharoen, W.; Phrommintikul, A. The protective role of curcumin in cardiovascular diseases. Int. J. Cardiol. 2009, 133, 145–151. [Google Scholar] [CrossRef] [PubMed]
  17. Park, W.; Ruhul Amin, A.R.M.; Chen, Z.G.; Shin, D.M. New perspectives of curcumin in cancer prevention. Cancer Prev. Res. (Phila) 2013, 6, 387–400. [Google Scholar] [CrossRef] [PubMed]
  18. Aggarwal, B.B.; Harikumar, K.B. Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases. Int. J. Biochem. Cell Biol. 2009, 41, 40–59. [Google Scholar] [CrossRef] [PubMed]
  19. Rivera-Espinoza, Y.; Muriel, P. Pharmacological actions of curcumin in liver diseases or damage. Liver Int. 2009, 29, 1457–1466. [Google Scholar] [CrossRef] [PubMed]
  20. Zhang, D.-W.; Fu, M.; Gao, S.-H.; Liu, J.-L. Curcumin and Diabetes: A Systematic Review. Evid. Based Complement. Altern. Med. 2013. [Google Scholar] [CrossRef] [PubMed]
  21. Akbik, D.; Ghadiri, M.; Chrzanowski, W.; Rohanizadeh, R. Curcumin as a wound healing agent. Life Sci. 2014, 116, 1–7. [Google Scholar] [CrossRef] [PubMed]
  22. Zheng, Z.; Sun, Y.; Liu, Z.; Zhang, M.; Li, C.; Cai, H. The effect of curcumin and its nanoformulation on adjuvant-induced arthritis in rats. Drug Des. Dev. Ther. 2015, 9, 4931–4942. [Google Scholar]
  23. He, Y.; Yue, Y.; Zheng, X.; Zhang, K.; Chen, S.; Du, Z. Curcumin, inflammation, and chronic diseases: How are they linked? Molecules 2015, 20, 9183–9213. [Google Scholar] [CrossRef] [PubMed]
  24. Ghosh, S.S.; Gehr, T.W.; Ghosh, S. Curcumin and chronic kidney disease (CKD): Major mode of action through stimulating endogenous intestinal alkaline phosphatase. Molecules 2014, 19, 20139–20156. [Google Scholar] [CrossRef] [PubMed]
  25. Yao, Y.; Wang, W.; Li, M.; Ren, H.; Chen, C.; Wang, J.; Wang, W.E.; Yang, J.; Zeng, C. Curcumin Exerts its Anti-hypertensive Effect by Down-regulating the AT1 Receptor in Vascular Smooth Muscle Cells. Sci. Rep. 2016. [Google Scholar] [CrossRef] [PubMed]
  26. Pescosolido, N.; Giannotti, R.; Plateroti, A.M.; Pascarella, A.; Nebbioso, M. Curcumin: Therapeutical potential in ophthalmology. Planta Med. 2014, 80, 249–254. [Google Scholar] [CrossRef] [PubMed]
  27. Chen, Z.; Xue, J.; Shen, T.; Mu, S.; Fu, Q. Curcumin alleviates glucocorticoid-induced osteoporosis through the regulation of the Wnt signaling pathway. Int. J. Mol. Med. 2016, 37, 329–338. [Google Scholar] [CrossRef] [PubMed]
  28. Thangapazham, R.L.; Sharma, A.; Maheshwari, R.K. Beneficial role of curcumin in skin diseases. Adv. Exp. Med. Biol. 2007, 595, 343–357. [Google Scholar] [PubMed]
  29. Ghalandarlaki, N.; Alizadeh, A.M.; Ashkani-Esfahani, S. Nanotechnology-Applied curcumin for different diseases therapy. BioMed. Res. Int. 2014. [Google Scholar] [CrossRef] [PubMed]
  30. Dende, C.; Meena, J.; Nagarajan, P.; Nagaraj, V.A.; Panda, A.K.; Padmanaban, G. Nanocurcumin is superior to native curcumin in preventing degenerative changes in Experimental Cerebral Malaria. Sci. Rep. 2017. [Google Scholar] [CrossRef] [PubMed]
  31. Prasad, S.; Aggarwal, B.B. Turmeric, the golden spice: From traditional medicine. In Herbal Medicine: Biomolecular and Clinical Aspects, 2nd ed.; Benzie, I.F.F., Wachtel-Galor, S., Eds.; CRC Press/Taylor & Francis: Boca Raton, FL, USA, 2011; ISBN 9781439807132. [Google Scholar]
  32. Wright, L.E.; Frye, J.B.; Gorti, B.; Timmermann, B.N.; Funk, J.L. Bioactivity of Turmeric-Derived Curcuminoids and Related Metabolites in Breast Cancer. Curr. Pharm. Des. 2013, 19, 6218–6225. [Google Scholar] [CrossRef] [PubMed]
  33. Lee, W.-H.; Loo, C.-Y.; Bebawy, M.; Luk, F.; Mason, R.S.; Rohanizadeh, R. Curcumin and its Derivatives: Their Application in Neuropharmacology and Neuroscience in the 21st Century. Curr. Neuropharmacol. 2013, 11, 338–378. [Google Scholar] [CrossRef] [PubMed]
  34. Alok, A.; Singh, I.D.; Singh, S.; Kishore, M.; Jha, P.C. Curcumin–Pharmacological Actions and its Role in Oral Submucous Fibrosis: A Review. J. Clin. Diagn. Res. 2015, 9, ZE01–ZE03. [Google Scholar] [CrossRef] [PubMed]
  35. Ucisik, M.H.; Kupcu, S.; Schuster, B.; Sleytr, U.B. Characterization of CurcuEmulsomes: Nanoformulation for enhanced solubility and delivery of curcumin. J. Nanobiotechnol. 2013. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Iriti, M.; Vitalini, S.; Fico, G.; Faoro, F. Neuroprotective Herbs and Foods from Different Traditional Medicines and Diets. Molecules 2010, 15, 3517–3555. [Google Scholar] [CrossRef] [PubMed]
  37. Maheshwari, R.; Singh, A.K.; Gaddipati, J.; Srimal, R.C. Multiple biological activities of curcumin: A short review. Life Sci. 2006, 78, 2081–2087. [Google Scholar] [CrossRef] [PubMed]
  38. Anand, P.; Thomas, S.G.; Kunnumakkara, A.B.; Sundaram, C.; Harikumar, K.B.; Sung, B.; Tharakan, S.T.; Misra, K.; Priyadarsini, I.K.; Rajasekharan, K.N.; et al. Biological activities of curcumin and its analogues (Congeners) made by man and Mother Nature. Biochem. Pharmacol. 2008, 76, 1590–1611. [Google Scholar] [CrossRef] [PubMed]
  39. Teow, S.-Y.; Liew, K.; Ali, S.A.; Khoo, A.S.; Peh, S.-C. Antibacterial action of curcumin against Staphylococcus aureus: A brief review. J. Trop. Med. 2016. [Google Scholar] [CrossRef] [PubMed]
  40. Alwi, I.; Santoso, T.; Suyono, S.; Sutrisna, B.; Suyatna, F.D.; Kresno, S.B.; Ernie, S. The effect of curcumin on lipid level in patients with acute coronary syndrome. Acta Med. Indones. 2008, 40, 201–210. [Google Scholar] [PubMed]
  41. Liu, Y. Curcumin: An Ingredient that Reduces Platelet Aggregation and Hyperlipidemia, and Enhances Antioxidant and Immune Functions. ACS Symp. Ser. 1997, 660, 199–205. [Google Scholar]
  42. Kim, D.C.; Ku, S.K.; Bae, J.S. Anticoagulant activities of curcumin and its derivative. BMP Rep. 2012, 45, 221–226. [Google Scholar] [CrossRef]
  43. Wang, N.P.; Wang, Z.F.; Tootle, S.; Philip, T.; Zhao, Z.Q. Curcumin promotes cardiac repair and ameliorates cardiac dysfunction following myocardial infarction. Br. J. Pharmacol. 2012, 167, 1550–1562. [Google Scholar] [CrossRef] [PubMed]
  44. Soetikno, V.; Suzuki, K.; Veeraveedu, P.T.; Arumugam, S.; Lakshmanan, A.P.; Sone, H.; Watanabe, K. Molecular understanding of curcumin in diabetic nephropathy. Drug Discov. Today 2013, 18, 756–763. [Google Scholar] [CrossRef] [PubMed]
  45. Qureshi, M.; Al-Suhaimi, E.A.; Wahid, F.; Shehzad, O.; Shehzad, A. Therapeutic potential of curcumin for multiple sclerosis. Neurol. Sci. 2017. [Google Scholar] [CrossRef] [PubMed]
  46. Lee, H.Y.; Kim, S.W.; Lee, G.H.; Choi, M.K.; Jung, H.W.; Kim, Y.J.; Kwon, H.J.; Chae, H.J. Turmeric extract and its active compound, curcumin, protect against chronic CCl4-induced liver damage by enhancing antioxidation. BMC Complement. Altern. Med. 2016. [Google Scholar] [CrossRef] [PubMed]
  47. Shanmugam, M.K.; Rane, G.; Kanchi, M.M.; Arfuso, F.; Chinnathambi, A.; Zayed, M.E.; Alharbi, S.A.; Tan, B.K.; Kumar, A.P.; Sethi, G. The multifaceted role of curcumin in cancer prevention and treatment. Molecules 2015, 20, 2728–2769. [Google Scholar] [CrossRef] [PubMed]
  48. Liu, X.-F.; Hao, J.-K.; Xie, T.; Mukhtar, N.J.; Zhang, W.; Malik, T.H.; Lu, C.-W.; Zhou, D.-D. Curcumin, a Potential Therapeutic Candidate for Anterior Segment Eye Diseases: A Review. Front. Pharmacol. 2017. [Google Scholar] [CrossRef] [PubMed]
  49. Beevers, C.S.; Huang, S. Pharmacological and clinical properties of curcumin. Botanics 2011. [Google Scholar] [CrossRef]
  50. Zhao, J.-F.; Ching, L.-C.; Huang, Y.-C.; Chen, C.-Y.; Chiang, A.-N.; Kou, Y.R.; Shyue, S.-K.; Lee, T.-S. Molecular mechanism of curcumin on the suppression of cholesterol accumulation in macrophage foam cells and atherosclerosis. Mol. Nutr. Food Res. 2012, 56, 691–701. [Google Scholar] [CrossRef] [PubMed]
  51. Naidu, K.A.; Thippeswamy, N.B. Inhibition of human low density lipoprotein oxidation by active principles from spices. Mol. Cell. Biochem. 2002, 229, 19–23. [Google Scholar] [CrossRef] [PubMed]
  52. Kempaiah, R.K.; Srinivasan, K. Integrity of erythrocytes of hypercholesterolemic rats during spices treatment. Mol. Cell Biochem. 2002, 236, 155–161. [Google Scholar] [CrossRef] [PubMed]
  53. Tuorkey, M.J. Curcumin a potent cancer preventive agent: Mechanisms of cancer cell killing. Interv. Med. Appl. Sci. 2014, 6, 139–146. [Google Scholar] [CrossRef] [PubMed]
  54. Sun, X.; Liu, Y.; Li, C.; Wang, X.; Zhu, R.; Liu, C.; Liu, H.; Wang, L.; Ma, R.; Fu, M.; et al. Recent Advances of Curcumin in the Prevention and Treatment of Renal Fibrosis. BioMed. Res. Int. 2017. [Google Scholar] [CrossRef] [PubMed]
  55. Ghorbani, Z.; Hekmatdoost, A.; Mirmiran, P. Anti-hyperglycemic and insulin sensitizer effects of turmeric and its principle constituent curcumin. Int. J Endocrinol. Metab. 2014. [Google Scholar] [CrossRef] [PubMed]
  56. Tang, M.; Taghibiglou, C. The mechanisms of action of curcumin in Alzheimer’s disease. J. Alzheimers Dis. 2017, 58, 1003–1016. [Google Scholar] [CrossRef] [PubMed]
  57. Li, G.; Bu, J.; Zhu, Y.; Xiao, X.; Liang, Z.; Zhang, R. Curcumin improves bone microarchitecture in glucocorticoid-induced secondary osteoporosis mice through the activation of microRNA-365 via regulating MMP-9. Int. J. Clin. Exp. Pathol. 2015, 8, 15684–15695. [Google Scholar] [PubMed]
  58. Kumar, K.; Rai, A.K. Curcumin: A yellow magical spice of kitchen for treatment of rheumatoid arthritis. Int. Res. J. Pharm. 2011, 2, 29–31. [Google Scholar]
  59. Shin, S.-K.; Ha, T.-Y.; McGregor, R.A.; Choi, M.-S. Long-term curcumin administration protects against atherosclerosis via hepatic regulation of lipoprotein cholesterol metabolism. Mol. Nutr. Food Res. 2011, 55, 1829–1840. [Google Scholar] [CrossRef] [PubMed]
  60. Anand, P.; Sundaram, C.; Jhurani, S.; Kunnumakkara, A.B.; Aggarwal, B.B. Curcumin and cancer: An “old-age” disease with an “age-old” solution. Cancer Lett. 2008, 267, 133–164. [Google Scholar] [CrossRef] [PubMed]
  61. Sikora, E.; Scapagnini, G.; Barbagallo, M. Curcumin, inflammation, ageing and age-related diseases. Immun. Ageing 2010. [Google Scholar] [CrossRef] [PubMed]
  62. Sundar, D.S.; Antoniraj, M.G.; Kumar, C.S.; Mohapatra, S.S.; Houreld, N.N.; Ruckmani, K. Recent Trends of Biocompatible and Biodegradable Nanoparticles in Drug Delivery: A Review. Curr. Med. Chem. 2016, 23, 3730–3751. [Google Scholar] [CrossRef] [PubMed]
  63. Baetke, S.C.; Lammers, T.; Kiessling, F. Applications of nanoparticles for diagnosis and therapy of cancer. Br. J. Radiol. 2015. [Google Scholar] [CrossRef] [PubMed]
  64. Flora, G.; Gupta, D.; Tiwari, A. Nanocurcumin: A promising therapeutic advancement over native curcumin. Crit. Rev. Ther. Drug Carrier Syst. 2013, 30, 331–368. [Google Scholar] [CrossRef] [PubMed]
  65. Ahmad, M.Z.; Akhter, S.; Mohsin, N.; Abdel-Wahab, B.A.; Ahmad, J.; Warsi, M.H.; Rahman, M.; Mallick, N.; Ahmad, F.J. Transformation of curcumin from food additive to multifunctional medicine: Nanotechnology bridging the gap. Curr. Drug Discov. Technol. 2014, 11, 197–213. [Google Scholar] [CrossRef] [PubMed]
  66. Ameruoso, A.; Palomba, R.; Palange, A.L.; Cervadoro, A.; Lee, A.; Mascolo, D.D.; Decuzzi, P. Ameliorating Amyloid-β Fibrils Triggered Inflammation via Curcumin-Loaded Polymeric Nanoconstructs. Front. Immunol. 2017. [Google Scholar] [CrossRef] [PubMed]
  67. Cheng, K.K.; Chan, P.S.; Fan, S.; Kwan, S.M.; Yeung, K.L.; Wang, Y.X.; Chow, A.H.; Wu, E.X.; Baum, L. Curcumin-conjugated magnetic nanoparticles for detecting amyloid plaques in Alzheimer’s disease mice using magnetic resonance imaging (MRI). Biomaterials 2015, 44, 155–172. [Google Scholar] [CrossRef] [PubMed]
  68. Dhivya, R.; Ranjani, J.; Rajendhran, J.; Mayandi, J.; Annaraj, J. Enhancing the anti-gastric cancer activity of curcumin with biocompatible and pH sensitive PMMA-AA/ZnO nanoparticles. Mater. Sci. Eng. C 2018, 82, 182–189. [Google Scholar] [CrossRef] [PubMed]
  69. Yallapu, M.M.; Khan, S.; Maher, D.M.; Ebeling, M.C.; Sundram, V.; Chauhan, N.; Ganju, A.; Balakrishna, S.; Gupta, B.K.; Zafar, N.; et al. Anti-cancer activity of curcumin loaded nanoparticles in prostate cancer. Biomaterials 2014, 35, 8635–8648. [Google Scholar] [CrossRef] [PubMed]
  70. Meena, R.; Kumar, S.; Kumar, R.; Gaharwar, U.S.; Rajamani, P. PLGA-CTAB curcumin nanoparticles: Fabrication, characterization and molecular basis of anticancer activity in triple negative breast cancer cell lines (MDA-MB-231 cells). Biomed. Pharmacother. 2017, 94, 944–954. [Google Scholar] [CrossRef] [PubMed]
  71. Fan, Y.; Yi, J.; Zhang, Y.; Yokoyama, W. Fabrication of curcumin-loaded bovine serum albumin (BSA)-dextran nanoparticles and the cellular antioxidant activity. Food Chem. 2018, 239, 1210–1218. [Google Scholar] [CrossRef] [PubMed]
  72. Wang, J.; Wang, H.; Zhu, R.; Liu, Q.; Fei, J.; Wang, S. Anti-inflammatory activity of curcumin-loaded solid lipid nanoparticles in IL-1b transgenic mice subjected to the lipopolysaccharide-induced sepsis. Biomaterials 2015, 53, 475–483. [Google Scholar] [CrossRef] [PubMed]
  73. Li, J.; Zhou, Y.; Zhang, W.; Bao, C.; Xie, Z. Relief of oxidative stress and cardiomyocyte apoptosis by using curcumin nanoparticles. Colloids Surf. B 2017, 153, 174–182. [Google Scholar] [CrossRef] [PubMed]
  74. Dewangan, A.K.; Perumal, Y.; Pavurala, N.; Chopra, K.; Mazumder, S. Preparation, characterization and anti-inflammatory effects of curcumin loaded carboxymethyl cellulose acetate butyrate nanoparticles on adjuvant induced arthritis in rats. J. Drug Deliv. Sci. Technol. 2017, 41, 269–279. [Google Scholar] [CrossRef]
  75. Ahn, J.; Jeong, J.; Lee, H.; Sung, M.-J.; Jung, C.H.; Lee, H.; Hur, J.; Park, J.H.; Jang, Y.J.; Ha, T.Y. Poly(lactic-co-glycolic acid) Nanoparticles Potentiate the Protective Effect of Curcumin against Bone Loss in Ovariectomized Rats. J. Biomed. Nanotechnol. 2017, 13, 688–698. [Google Scholar] [CrossRef]
  76. Li, M.; Xin, M.; Guo, C.; Lin, G.; Wu, X. New nanomicelle curcumin formulation for ocular delivery: Improved stability, solubility, and ocular anti-inflammatory treatment. Drug Dev. Ind. Pharm. 2017, 43, 1846–1857. [Google Scholar] [CrossRef] [PubMed]
  77. Lin, Y.L.; Liu, Y.K.; Tsai, N.M.; Hsieh, J.H.; Chen, C.H.; Lin, C.M.; Liao, K.W. A Lipo-PEG-PEI complex for encapsulating curcumin that enhances its antitumor effects on curcumin-sensitive and curcumin-resistance cells. Nanomedicine 2012, 8, 318–327. [Google Scholar] [CrossRef] [PubMed]
  78. Montalban, M.G.; Coburn, J.M.; Lozano-Perez, A.A.; Cenis, J.L.; Villora, G.; Kaplan, D.L. Production of curcumin-loaded silk fibroin nanoparticles for cancer therapy. Nanomaterials 2018. [Google Scholar] [CrossRef] [PubMed]
  79. Sunagawa, Y.; Wada, H.; Suzuki, H.; Sasaki, H.; Imaizumi, A.; Fukuda, H.; Hashimoto, T.; Katanasaka, Y.; Shimatsu, A.; Kimura, T.; et al. A Novel Drug Delivery System of Oral Curcumin Markedly Improves Efficacy of Treatment for Heart Failure after Myocardial Infarction in Rats. Biol. Pharm. Bull. 2012, 35, 139–144. [Google Scholar] [CrossRef] [PubMed]
  80. Young, N.A.; Wu, L.-C.; Gardner, M.; Hampton, J.; Bruss, M.; Jarjour, W. AB0185 Nano-Emulsified Curcumin (NEC), a Patented Anti-Inflammatory Nutraceutical Compound Developed at Ohio State, Reduces Renal Pathology in an Animal Model of Lupus Nephritis. Ann. Rheum. Dis. 2015, 74, 952–953. [Google Scholar] [CrossRef]
  81. Chen, X.; Sun, J.; Li, H.; Wang, H.; Lin, Y.; Hu, Y.; Zheng, D. Curcumin-Loaded Nanoparticles Protect Against Rhabdomyolysis-Induced Acute Kidney Injury. Cell. Physiol. Biochem. 2017, 43, 2143–2154. [Google Scholar] [CrossRef] [PubMed]
  82. Cheng, K.K.; Yeung, C.F.; Ho, S.W.; Chow, S.F.; Chow, A.H.L.; Baum, L. Highly Stabilized Curcumin Nanoparticles Tested in an in Vitro Blood–Brain Barrier Model and in Alzheimer’s Disease Tg2576 Mice. AAPS J. 2013, 15, 324–336. [Google Scholar] [CrossRef] [PubMed]
  83. Grama, C.N.; Suryanarayana, P.; Patil, M.A.; Raghu, G.; Balakrishna, N.; Ravi Kumar, M.N.V.; Reddy, G.B. Efficacy of Biodegradable Curcumin Nanoparticles in Delaying Cataract in Diabetic Rat Model. PLoS ONE 2013. [Google Scholar] [CrossRef] [PubMed]
  84. Heo, D.N.; Ko, W.-K.; Moon, H.-J.; Kim, H.-J.; Lee, S.J.; Lee, J.B.; Bae, M.S.; Yi, J.K.; Hwang, Y.S.; Bang, J.B.; et al. Inhibition of Osteoclast Differentiation by Gold Nanoparticles Functionalized with Cyclodextrin Curcumin Complexes. ACS Nano 2014, 8, 12049–12062. [Google Scholar] [CrossRef] [PubMed]
  85. Effects of Short-Term Curcumin and Multi-Polyphenol Supplementation on the Anti-Inflammatory Properties of HDL (PSI). Available online: https://clinicaltrials.gov/ct2/show/NCT02998918 (accessed on 25 January 2018).
  86. Curcumin in Preventing Colorectal Cancer in Patients Undergoing Colorectal Endoscopy or Colorectal Surgery. Available online: https://clinicaltrials.gov/ct2/show/record/NCT00973869 (accessed on 25 January 2018).
  87. The Effect of Diet on Chronic Inflammation and Related Disorders Following Spinal Cord Injury. Available online: https://clinicaltrials.gov/ct2/show/record/NCT02099890 (accessed on 25 January 2018).
  88. Micro-Particle Curcumin for the Treatment of Chronic Kidney Disease (MPAC-CKD). Available online: https://clinicaltrials.gov/ct2/show/NCT02369549 (accessed on 25 January 2018).
  89. Effects of Curcumin Supplementation on Lipid Profile and Inflammatory Markers of Patients with Type 2 Diabetes. Available online: https://clinicaltrials.gov/ct2/show/NCT02529969 (accessed on 25 January 2018).
  90. Safety and Efficacy of Anti-Oxidants and Anti-Inflammatory Agents in Glaucoma and Diabetic Retinopathy. Available online: https://clinicaltrials.gov/ct2/show/NCT02984813 (accessed on 25 January 2018).
  91. A Pilot Study of Curcumin and Ginkgo for Treating Alzheimer’s Disease. Available online: https://clinicaltrials.gov/ct2/show/NCT00164749 (accessed on 25 January 2018).
  92. Curcumin in Rheumatoid Arthritis. Available online: https://clinicaltrials.gov/ct2/show/NCT00752154 (accessed on 25 January 2018).
Figure 1. (a) Chemical structure of curcumin; and (b) annual publication history of curcumin (2008–2017).
Figure 1. (a) Chemical structure of curcumin; and (b) annual publication history of curcumin (2008–2017).
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Figure 2. Annual publication history (2008–2017) of curcumin with different aging-associated diseases generated from the “Scopus” database, using the keywords (a) atherosclerosis-curcumin, (b) cancer-curcumin; (c) cardiovascular diseases-curcumin (d) chronic inflammation-curcumin; (e) chronic kidney diseases-curcumin; (f) diabetes-curcumin; (g) hypertension-curcumin; (h) neurodegenerative diseases-curcumin; (i) ocular diseases-curcumin; (j) osteoporosis-curcumin; and (k) rheumatoid arthritis-curcumin.
Figure 2. Annual publication history (2008–2017) of curcumin with different aging-associated diseases generated from the “Scopus” database, using the keywords (a) atherosclerosis-curcumin, (b) cancer-curcumin; (c) cardiovascular diseases-curcumin (d) chronic inflammation-curcumin; (e) chronic kidney diseases-curcumin; (f) diabetes-curcumin; (g) hypertension-curcumin; (h) neurodegenerative diseases-curcumin; (i) ocular diseases-curcumin; (j) osteoporosis-curcumin; and (k) rheumatoid arthritis-curcumin.
Molecules 23 00835 g002aMolecules 23 00835 g002b
Table 1. Diverse range of mechanisms of action of curcumin in aging-associated diseases.
Table 1. Diverse range of mechanisms of action of curcumin in aging-associated diseases.
Aging-Associated DiseasesMechanism of Action References
Atherosclerosis Reduces cholesterol accumulation; downregulates SR-A and upregulates ABCA1 by a proteasome and LXRα dependent pathway; inhibition of low density lipoprotein oxidation; stabilization of cell membrane cholesterol.[50,51,52]
CancerInduction of apoptotic signal; suppression of anti-apoptotic proteins; modulates miRNAs, Wnt/β-Catenin signals, protein kinases, and proteasome activation; inhibition of NF-κB; reverses the multidrug resistance of cancer cells.[53]
Cardiovascular diseasesAnti-oxidant (inhibits eNOS, and iNOS); inhibits sarcoplasmic Ca2+-ATPase; membrane stabilizing effect; prevents Adriamycin-induced cardiomyopathy; prevents diabetic cardiovascular complications; inhibits p300 and NF-κB; decreases serum cholesterol levels.[16]
Chronic inflammationAlleviates oxidative stress; suppress pro-inflammatory pathways; TNF blocker.[23]
Chronic kidney diseasesReduces inflammatory molecules MCP-1, NF-κB, TNF-α, IL-1β, COX-2 and cav-1; induces the expression of anti-inflammatory factors such as HO-1, M6PRBP1, and NEDD4.[54]
DiabetesReduces oxidative stress; reduction of blood glucose levels; stimulates insulin production. [55]
HypertensionReduces AT1R mediated vasoconstriction. [25]
Neurodegenerative diseasesLowers cholesterol levels; inhibits amyloid-β; modulates microglia; Acetylcholinesterase and Tau inhibition; copper binding; anti-oxidant properties.[56]
Ocular diseasesNeuroprotection in glaucoma; anti-inflammation activities in anterior uveitis and dry eye; anti-allergy in conjunctivitis; anti-proliferation activities and promotes apoptosis in pterygium; inhibits neovascularization; anti-oxidative stress in cataracts; protects epithelial barriers and promotes wound healing in corneal diseases.[48]
OsteoporosisSuppresses the expression of MMP-9; protective effect against bone deterioration. [57]
Rheumatoid arthritisAnti-inflammatory activity; inhibits enzymes involved in inflammation (COX-2); downregulates the activation of transcription factor NF-κB and expression of other inflammatory intermediate molecules (TNF-α, adhesion molecules, MMPs, COX-2, and 5-LOX) associated with arthritis. [58]
ABCA1—ATP binding cassette family member 1; LXRα-Liver X receptor alpha; miRNAs—microRNAs; eNOS—endothelial nitric oxide synthase; NF-κB-Nuclear factor kappa B; iNOS—Inducible nitric oxide synthase; TNF—Tumor necrosis factor; MCP-1-Monocyte Chemoattractant Protein-1; IL-1β—Interleukin 1 beta; COX-2 —Cyclooxygenase 2; cav-1—Caveolin 1; HO-1—Heme oxygenase 1; M6PRBP1-Mannose-6-phosphate receptor binding protein 1; NEDD4-neural precursor cell expressed developmentally down-regulated protein 4; AT1R-Angiotensin II receptor type 1; MMP-9—Matrix metallopeptidase 9; MMPs—Matrix metalloproteinase; 5-LOX—5 lipoxygenase.
Table 2. Therapeutic potential of curcumin used in the treatment of aging-associated diseases.
Table 2. Therapeutic potential of curcumin used in the treatment of aging-associated diseases.
Aging-Associated DiseasesTherapeutic Potential of CurcuminOutcomesReferences
Atherosclerosis Anti-atherogenic effect of curcumin via different mechanisms.The effect of curcumin was studied and compared with the drug lovastatin, and the long-term treatment with curcumin lowered plasma and hepatic cholesterol, and suppressed early atherosclerotic lesions.[59]
CancerCurcumin interferes with multiple cell signaling pathways which include cell cycle, apoptosis, proliferation, angiogenesis, invasion, metastasis and inflammation.The anticancer activity of curcumin was reported against different cancers, and it plays a significant role in different cell signaling pathway and numerous molecular targets. The in vitro, in vivo and clinical studies revealed the therapeutic value of curcumin for the treatment of “old-age“ diseases like cancer. [60]
Cardiovascular diseasesThe inflammatory effects of curcumin may play a key role in the prevention of cardiovascular diseases.Curcumin showed the possibility of preventing atrial arrhythmias and some ventricular arrhythmias. [16]
Chronic inflammationCurcumin can suppress both acute and chronic inflammation by scavenging reactive oxygen species and enhancing antioxidant defences.Curcumin shows very good antioxidant properties, and it plays a key role in the prevention and treatment of chronic inflammation.[23,61]
Chronic kidney diseasesCurcumin increases the expression of intestinal alkaline phosphatase and tight junction proteins. The study shows the potential anti-inflammatory effects of curcumin and their positive effects for the treatment of chronic kidney diseases.[24]
DiabetesCurcumin reduces glycemia and hyperlipidemia in rodent models, and favourably affects some leading aspects of diabetes which include insulin resistance, hyperglycemia and islet apoptosis and necrosis.Curcumin is actively involved in the prevention and treatment of diabetes. The study showed that curcumin and their complexes can successfully be used for the treatment of various disorders associated with diabetes such as liver disorders, adipose tissue dysfunction, diabetic neuropathy, diabetic nephropathy, diabetic vascular disease, and other complications associated with diabetes. [20]
HypertensionCurcumin shows beneficial effects on hypertension; it prevents the development of hypertension by regulating AT1 receptor expression.The study was performed using curcumin in an Ang II-induced hypertensive model, and it showed that curcumin aids in the downregulation of the AT1 receptor in A10 cells and it subsequently prevents hypertension.[25]
Neurodegenerative diseasesCurcumin has reported to be an effective neuroprotective agent and it may prevent aging associated changes in cellular proteins.Protein homeostasis plays an important role in aging-associated diseases. The study performed in an invertebrate model (Caenorhabditis elegans) showed that the drug curcumin aids to maintain protein homeostasis and increases the life span of the model organism. Several animal model studies showed that curcumin prevents or delays various neurodegenerative diseases.[14]
Ocular diseasesCurcumin exhibits potential therapeutic activity against several ocular diseases.Curcumin showed beneficial effects in the prevention and treatment of several ocular diseases. The dosage of curcumin, up to 8g/day for three months, does not produce any dose-limiting toxicity in pharmacological studies. Clinical data proved that the few weeks of curcumin treatment reduced the signs and symptoms of eye discomfort and is safe in the treatment of humans.[26]
OsteoporosisCurcumin may be a potential candidate for the treatment of osteoporosis. The protective effects of curcumin were studied against dexamethasone induced osteoporosis in a rat model. The results proved that curcumin effectively prevented glucocorticoid- induced osteoporosis.[27]
Rheumatoid arthritisCurcumin possess various pharmacological activities including antiarthritic effects.The effect of curcumin was studied in an adjuvant-induced arthritis rat model, and it showed similar therapeutic effects for the treatment of rheumatoid arthritis compared with the drug methotrexate.[22]
Table 3. Recent advances in the preparation of nanocurcumin for the treatment of aging-associated diseases.
Table 3. Recent advances in the preparation of nanocurcumin for the treatment of aging-associated diseases.
Aging-Associated DiseasesDetail of NanoparticlesSize (nm)OutcomesReferences
CancerCurcumin loaded cationic liposome- polyethylene glycol (PEG) and poly (ethylene imine) complex270 nmCurcumin liposomes showed five-fold cytotoxic activity on curcumin-sensitive cells and twenty-fold against curcumin-resistant cells compared to native curcumin, and achieved 45 ± 0.2% curcumin encapsulation efficiency in the liposome complex. In vivo studies showed that the administration of curcumin liposomes inhibited 60–90% of tumor growth. [77]
CancerCurcumin loaded silk fibroin nanoparticles 155–170 nmCurcumin loaded silk fibroin nanoparticles were synthesized using both physical adsorption (drug loading content of 6.63 ± 0.09% and encapsulation efficiency of 53.75 ± 0.81%) and co-precipitation (drug loading content of 2.47 ± 0.11% and encapsulation efficiency of 48.84 ± 2.67%). The synthesized material showed excellent antitumor activity against both Hep3B and Kelly cells.[78]
Cardiovascular diseasesColloidal nanoparticles (Curcumin with gum ghatti solution)190 nmA small amount of synthesized colloidal curcumin nanoparticles could be more therapeutically effective for heart failure than native curcumin.[79]
Chronic inflammationNano-emulsified curcumin (NEC)-NEC was orally supplied to NZM2410 mice (lupus nephritis model) and kidney function was monitored by testing blood urea nitrogen. Results suggested that NEC has a good therapeutic potential in the treatment of chronic inflammation and other autoimmune diseases.[80]
Chronic kidney diseasesCurcumin nanoparticles80–100 nmThe in vitro and in vivo study suggested that the curcumin nanoparticles enhanced the treatment efficacy of Rhabdomyolysis induced acute kidney injury than free curcumin. The release study was performed using dialysis. The initial 20 h of dialysis showed that upto 40% of curcumin nanoparticles were released and 80% of free curcumin was released. Nanoparticulate curcumin achieved prolonged release profile than free curcumin.[81]
Neurodegenerative diseasesNanocurcumin (Curcumin loaded p(PEG-poly-lactic acid) micelles80 nmThere was improved bioavailability of nanocurcumin in the brains of Tg2576 mice as compared to free curcumin, and nanocurcumin showed positive effects in the treatment of Alzheimer’s disease. The entrapment efficiency of curcumin was almost 100% and the loading efficiency of curcumin was 37.6%. [82]
Ocular diseasesCurcumin encapsulated PLGA nanoparticles282.50 ± 5.72 nmThe study demonstrated the potential of curcumin encapsulated nanoparticles in managing diabetic cataracts in a streptozotocin induced diabetic rat cataract model. The enhanced performance of nanocurcumin was observed in different biochemical pathways than free curcumin. It may be due to the improved oral bioavailability of curcumin.[83]
OsteoporosisGold nanoparticles functionalized with cyclodextrin curcumin complexes36.3 nmLoading efficiency of curcumin was around 38.95% and the curcumin loaded nanoparticle complex showed an effective intracellular uptake and acts as a potential therapeutic agent in the treatment of bone diseases associated with excessive bone resorption.[84]
Rheumatoid arthritisCurcumin nanoemulsion (curcumin, solutol-HS 15, soybean oil)150 nmIn vivo rat study showed that the synthesized curcumin nanoemulsion acts as an effective antiarthritic agent. The oral route of curcumin nanoemulsion showed threefold increase of AUC (area under the curve) and Cmax value than the suspension (intravenous (iv) route) and it significantly enhanced the drug absorption than free curcumin. Overall, the in vivo rat study suggested that the nanoform of curcumin aids to convert the therapy route from iv to oral administration for the effective treatment of RA therapy[22]
Table 4. Number of clinical trials generated from the “https://clinicaltrials.gov” database using the keywords (curcumin and the different aging-associated diseases).
Table 4. Number of clinical trials generated from the “https://clinicaltrials.gov” database using the keywords (curcumin and the different aging-associated diseases).
Keywords UsedNo. of Studies Found
Atherosclerosis-curcumin1
Cancer-curcumin57
Cardiovascular diseases-curcumin9
Chronic inflammation-curcumin2
Chronic kidney diseases-curcumin5
Diabetes-curcumin11
Hypertension-curcumin1
Neurodegenerative diseases-curcumin6
Ocular diseases-curcumin4
Osteoporosis-curcumin0
Rheumatoid arthritis-curcumin 2
Table 5. Status of some of the major global clinical trials of curcumin in aging-associated diseases.
Table 5. Status of some of the major global clinical trials of curcumin in aging-associated diseases.
ClinicalTrials.gov IdentifierAges (Years)DiseaseDoses of CurcuminPhase Reference
NCT0299891818 to 60 (Adult)Inflammation
Atherosclerosis
Cardiovascular Disease
500 mg of curcumin phytosome twice daily for 1 week2[85]
NCT0097386918 and older (Adult, Senior)Colorectal cancerOral curcumin once daily for 14–28 days1[86]
NCT0209989018 and older (Adult, Senior)Neuropathic pain;
Depression;
Cognitive impairment;
Somatic neuropathy;
Autonomic dysfunction
InflanNox capsule (400 mg curcumin) taken 3 times daily along with other anti-inflammatory supplements3[87]
NCT0236954918 and older (Adult, Senior)Chronic kidney diseaseThree 30 mg capsules of micro-particle curcumin daily in the morning3[88]
NCT0252996940 to 65 (Adult)Non-insulin dependent diabetes500 mg curcumin capsule2[89]
NCT0298481318 and older (Adult, Senior)Open-angle glaucoma diabetic retinopathyTwo pills daily (one contains curcumin and other contains active compounds) for 3 months 1[90]
NCT0016474950 and older (Adult, Senior)Alzheimer’s diseaseTwo different dosages (1 g/day and 4 g/day) along with ginkgo extract2[91]
NCT0075215418 and older (Adult, Senior)Rheumatoid arthritisCurcumin (Longvida™) 4 capsules approximately 2 g/day for 2 weeks, then the dose will be increased to 4 capsules twice a day (4 g/day)Early phase 1[92]

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Sundar Dhilip Kumar, S.; Houreld, N.N.; Abrahamse, H. Therapeutic Potential and Recent Advances of Curcumin in the Treatment of Aging-Associated Diseases. Molecules 2018, 23, 835. https://doi.org/10.3390/molecules23040835

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Sundar Dhilip Kumar S, Houreld NN, Abrahamse H. Therapeutic Potential and Recent Advances of Curcumin in the Treatment of Aging-Associated Diseases. Molecules. 2018; 23(4):835. https://doi.org/10.3390/molecules23040835

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Sundar Dhilip Kumar, Sathish, Nicolette Nadene Houreld, and Heidi Abrahamse. 2018. "Therapeutic Potential and Recent Advances of Curcumin in the Treatment of Aging-Associated Diseases" Molecules 23, no. 4: 835. https://doi.org/10.3390/molecules23040835

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