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. 2019 Dec 12;43(2):272–274. doi: 10.1007/s12272-019-01194-1

Correction to: Pharmacology of natural radioprotectors

Gil-Im Mun 1,#, Seoyoung Kim 1,#, Eun Choi 1, Cha Soon Kim 2,, Yun-Sil Lee 1,
PMCID: PMC7052032  PMID: 31832995

Correction to: Arch. Pharm. Res. 10.1007/s12272-018-1083-6

We apologize that there are some errors in the references for three sentences and table 2.

  1. In the section “Naturally occurring radioprotectors”, the reference of the first paragraph’s last sentence should be changed from ‘(Yu et al. 2003)’ to ‘(Praetorius and Mandal 2008)’.

Indeed, amifostine has several clinically relevant limitations, including (1) an administration time within a narrow window (15–30 min before IR exposure); (2) approval only for intravenous (IV) administration (Praetorius and Mandal 2008); and (3) high toxicity associated with undesirable side effects including nausea, vomiting, cephalalgia, and hypotension.

  • 2.

    In the section “Ferulic acid”, the reference of sixth sentence should be changed from ‘(Srinivasan et al. 2006)’ to ‘(Prasad et al. 2006)’.

Pretreatment of lymphocytes and hepatocytes with ferulic acid resulted in a significant decrease in DNA damage and lipid peroxidation after IR exposure (Prasad et al. 2006).

  • 3.

    In the section “Hesperidin”, the reference of fourth sentence should be changed from ‘(Fardid et al. 2016)’ to ‘(Hosseinimehr et al. 2009)’.

Additionally, hesperidin was shown to protect against genetic damage to lymphocytes induced by the radiotracer 99mTc-MIBI in vitro (Hosseinimehr et al. 2009).

  • 4.
    In connection to these errors, the following articles should be deleted in the References section:
    • Fardid R, Ghorbani Z, Haddadi G, Behzad-Behbahani A, Arabsolghar R, Kazemi E, Okhovat MA, Hosseinimehr SJ (2016) Effects of hesperidin as a radio-protector on apoptosis in rat peripheral blood lymphocytes after gamma radiation. J Biomed Phys Eng 6:217–228
    • Srinivasan M, Rajendra Prasad N, Menon VP (2006) Protective effect of curcumin on gamma-radiation induced DNA damage and lipid peroxidation in cultured human lymphocytes. Mutat Res 611:96–103
    • Yu Z, Eaton JW, Persson HL (2003) The radioprotective agent, amifostine, suppresses the reactivity of intralysosomal iron. Redox Rep 8:347–355
  • 5.
    Instead, following articles should be added to the References section:
    • Hosseinimehr SJ, Ahmadi A, Beiki D, Habibi E, Mahmoudzadeh A (2009) Protective effects of hesperidin against genotoxicity induced by 99mTc-MIBI in human cultured lymphocyte cells. Nucl Med Biol 36:863–867
    • Praetorius NP, Mandal TK (2008) Alternate delivery route for amifostine as a radio-/chemo-protecting agent. J Pharm Pharmacol 60:809–815
    • Prasad NR, Srinivasan M, Pugalendi KV, Menon VP (2006) Protective effect of ferulic acid on gamma-radiation-induced micronuclei, dicentric aberration and lipid peroxidation in human lymphocytes. Mutat Res 603:129–134
  • 6.
    In Table 2, three references should be corrected.
    • ‘Hall and Giaccia (2012)’ for caffeine should be corrected to ‘Kamat et al. (2000)’.
    • ‘Farooqi and Kesavan (1992)’ should be added for caffeine.
    • ‘Fardid et al. (2016)’ for hesperidin should be corrected to ‘Shaban et al. (2017)’.
  • 7.

    In the section “N-Acetyl Tryptophan Glucopyranoside (NATG)”, the word of first sentence should be changed from ‘Bacillus subtilis’ to ‘Bacillus sp. INM-1’.

Table 2.

List of naturally occurring compounds with radioprotective effects

Natural compounds Source Radioprotective effects References
Apigenin Parsley, Celery, Chamomile Anti-inflammatory, anti-proliferative, and anti-progression Begum et al. (2012)
Bergenin Caesalpinia digyna Activation of the MAP kinase and ERK pathways and protection against radiation damage

Dwivedi et al. (2017)

Veerapur et al. (2009)

Caffeine Coffee beans

Protection against the oxic component of damage in rat liver mitochondria

Inhibition of radiation-mediated chromosomal aberrations in mouse bone marrow cells

Farooqi and Kesavan (1992)

Kamat et al. (2000)

Chlorogenic acid/quinic acid Cinchona bark, Coffee beans Anti-inflammation, anti-mutagenic, DNA damage inhibition, and anti-oxidation Cinkilic et al. (2013)
Coniferyl aldehyde Eucommia ulmoides Induction of heat shock transcription factor 1 and protection against radiation damage

Kim et al. (2015)

Nam et al. (2013)

Curcumin Turmeric root

Reduction of gastrointestinal symptoms during chemotherapy and radiation therapy

Reduction of mucositis during radiation therapy

Reduction of radiation dermatitis and desquamation

Verma (2016)
Delphinidin Carrot, Tomato, Red onion, Cranberries, Concord grapes, etc Anti-oxidation and anti-inflammation

Jeong et al. (2016)

Watson and Schonlau (2015)

Epigallocatechin-3-gallate Camellia sinensis

Increased levels of several anti-oxidant enzymes

Protection of skin cells against radiation-induced damage and radioprotective effects against several radiation-mediated responses

Zhang et al. (2016)

Zhu et al. (2016)

Ferulic acid Rice, Green tea, Coffee beans

Protection against radiation-induced damage and enhancement of DNA repair

Prevention of radiation-induced micronuclei and dicentric aberrations in human lymphocytes

Enhancement of survival in mice after radiation

Das et al. (2014)

Kikuzaki et al. (2002)

Zhao et al. (2003)

Genistein Genista tictoria, etc.

Protection against acute radiation injury

Multiple mechanisms (e.g., antioxidant, free radical scavenger, anti-inflammatory, activation of the DNA repair enzyme Gadd45

Ahmad et al. (2010)

Davis et al. (2007)

Grace et al. (2007)

Hesperidin Citrus fruit

Efficient radioprotection in rat lung tissue

Protection of lipid peroxidation during radiation-induced tissue damage in rats

Rezaeyan et al. (2016)

Shaban et al. (2017)

Lycopene Tomato, Watermelon, Pink grapefruit, Papaya, etc

Protection against radiation-induced chromosomal damage in human lymphocytes

Increased survival after radiation exposure

Kelkel et al. (2011)

Srinivasan et al. (2009)

N-Acetyl tryptophan glucopyranoside (NATG) Bacillus sp. INM-1

Overcoming radiation-induced apoptosis by improving cytoprotective cytokines

Enhancement of antioxidant enzymes against radiation-induced damage

Malhotra et al. (2015)

Malhotra et al. (2018)

Psoralidin Psoralea corylifolia

Inhibition of radiation-induced PI3K-IKK-IκB signaling pathway and COX-2 expression

Suppression of radiation-induced expression of pro-inflammatory cytokines

Chiou et al. (2011)

Yang et al. (2011)

Sesamol Sesame seeds, Sesame oil Strong ROS scavenging and antioxidant properties

Kanimozhi and Prasad (2009)

Mishra et al. (2011)

Troxerutin Sophora japonica

Protection against radiation-induced damage to the salivary glands and mucosa

Inhibition of lipid peroxidation in the membranes of subcellular organelles

Differential protection of normal cells in irradiated tumor-bearing mice: protection in blood leukocytes and bone marrow cells but not in tumor cells

Maurya et al. (2004)
Vanillin Vanilla orchid (Vanilla planifolia, V. fragrans)

Suppression of radiation-induced chromosomal aberrations in cells and in mice

Anti-mutagenic effects

Kumar et al. (2000)
Zingerone Ginger Anti-oxidation

Ahmad et al. (2015)

Rao and Rao (2010)

Zymosan A Saccharomyces cerevisiae

Protection from radiation-induced apoptosis by upregulating the levels of cytokines

Protection of cells from radiation-induced DNA damage

Du et al. (2018)

Footnotes

Publisher’s Note

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Contributor Information

Cha Soon Kim, Email: chasoon.kim@khnp.co.kr.

Yun-Sil Lee, Email: yslee0425@ewha.ac.kr.


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