Radioprotective Activities of Podophyllum hexandrum: Current Knowledge of the Molecular Mechanisms

Raj Kumar, Pankaj Kumar Singh, Rajesh Arora, Raman Chawla, Rakesh Kumar Sharma

Studies are beginning to show the ability of some plant extracts to protect against radiation. This review highlights the radioprotective effects of the Himalayan Mayapple.

Raj Kumar, Pankaj Kumar Singh, Rajesh Arora, Raman Chawla, Rakesh Kumar Sharma*

Institute of Nuclear Medicine and Allied Sciences, Brig S.K. Mazumdar Road, Delhi-110 054, INDIA. *Corresponding author


Trees for Life Journal 2008, Vol 4:1

The electronic version of this article is the complete one and can be found online at:

Received: April 13, 2007; Accepted: September 6, 2007; Published: June 15, 2009

Copyright: ©2009 Rakesh Kumar Sharma et al.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

This is the second article published in the Trees for Life Journal which deals with radioprotection (see Role of Rosemary Leaf Extract Against Various Doses of Gamma Radiation by Sancheti and Goyal). While it is not a major focus of this journal, radioprotection has interest for our readership and is attracting ever more attention within the scientific community. No synthetic radioprotective chemicals are available that are perfectly safe and effective. While a variety of plant extracts have been evaluated for their protective capacity, this work is still in its infancy. The following review highlights the radioprotective effects of the Himalayan Mayapple. It also illustrates the degree to which mechanism-based studies are beginning to support the purely observational work that initially brought to light the radioprotective effects of certain plant extracts.


Radiation mediated free radical flux interferes with oxidation/reduction-based physiological mechanisms. These free radicals react with a number of biomolecules including Deoxyribonucleic acid (DNA), lipids and proteins. The rate and selectivity of these free radical mediated reactions depend upon the concentration, half-life and state of delocalization of electrons in the free radicals and the free radicals’ oxidizing ability.

Podophyllum hexandrum Royle (Himalayan Mayapple) was known as Aindri (“a divine drug”) in ancient times. It has been reported to be used through the ages and in modern times as a cure for allergic and inflammatory conditions of the skin; biliary fever; burning sensation; cold; constipation; cancer of the brain, bladder and lung; erysipelas; Hodgkin’s disease; insect bites; mental disorders; monocytoid leukemia; non-Hodgkin’s lymphoma; rheumatism; septic wounds; plague; and venereal warts. It has served as a commercial source of podophyllotoxin and related aryltetralin lignans and several other bioactive constituents. Podophyllotoxin finds use as a precursor for the semi-synthetic topisomerase inhibitors in the treatment of leukemias, lung and testicular cancers, dermatological disorders like warts, rheumatoid arthritis, psoriasis and malaria. It also has numerous applications in modern medicine by virtue of its free radical scavenging capacity. An extract of P. hexandrum has been shown to provide approximately 80% whole-body radioprotection in mice.

The present review highlights the state of knowledge about the radioprotective mechanism of P. hexandrum at different levels of organization in living organisms. Further, an insight into its mode of action at the molecular level, including the studies of the expression patterns of various proteins associated with inhibition of apoptosis in the spleen of male Swiss albino strain ‘A’ mice by immunoblotting, has been presented. In conclusion, the studies clearly demonstrated that P. hexandrum extract provides protection from gamma-radiation by the modulation of expression of proteins associated with cell death attributed to its ability to modulate free radical flux.


Radiation is one of the most severe causes of oxidative stress mediated by free radical flux. This flux interferes with oxidation/reduction-based physiological mechanisms existing inside the mammalian body system. The rate and selectivity of free radical mediated reaction depends primarily upon several factors: the concentration of radicals, the state of delocalization of electrons, the half-life of free radicals and weak bonds of nearby bio-molecules. Radiation protection is an area of great significance due to its possible applications in planned radiotherapy as well as unplanned radiation exposure (1,2). Research in the development of radioprotectors worldwide has focused on screening a variety of chemical and biological compounds. Various drugs from natural or synthetic origin, i.e., antioxidant cytoprotective agents, immuno modulators, vitamins and DNA binding molecules, have been evaluated extensively for their radioprotective potentials in both in vitro and in vivo models (1,3,4,5,6). However, the fact remains that there is not a single radioprotective drug available which meets all the prerequisites of an ideal radioprotector, i.e., produces no cumulative or irreversible toxicity, provides effective long-term protection, remains stable for a number of years without losing shelf life, and can be easily administered (7,8). In view of this, the search for less toxic and more potent radioprotector drugs continues.

Herbal drugs have been utilized since ancient times for curing various diseases and other disorders. Even today, more than 70% of the world’s population still depends on plant-based remedies to meet their health care needs (9). Various plants have been reported to be beneficial for free radical-mediated conditions in humans such as arthritis, atherosclerosis, cancer, Alzheimer’s disease, Parkinson’s disease, aging and inflammatory disorders. It is, therefore, logical to expect that plants may contain groups of compounds that can protect against radiation-induced reactive oxygen species (ROS) and reactive nitrogen species (RNS) mediated damage (7,8).

Podophyllum hexandrum

Podophyllum hexandrum Royle (Himalayan Mayapple), is an herb that grows at about 4000 meters of altitude in the Himalayan region (Figure 1) (10). P. hexandrum has been investigated extensively for its radioprotective capabilities in recent years, including free radical scavenging, time and dose-dependent inhibition of apoptosis (programmed cell death) and cell cycle arrest-related activities in both in vitro and in vivo models (7,8). The plant is an endangered species and included in the Red Book. In vitro propagation for mass multiplication of P. hexandrum has been recently reported (11). Besides its traditional uses (10), methanolic, hydro-alcoholic and chloroform extracts of P. hexandrum have been reported to render approximately 70-95% radioprotection in mice when administered 1-2 hours before lethal whole-body 10Gy radiation (12,13,14). To achieve radioprotection, recovery of damaged cells after radiation exposure and minimization of cell death by inhibition of apoptosis is an inescapable necessity (15,16,17,18,19). P. hexandrum has been reported to contain a number of bioactive molecules including flavonoids and lignans (10,20,21,22).

Figure 2(Click to enlarge)

Figure 1: Podophyllum hexandrum (syn. P. emodi); common names - Aindri, Himalayan Mayapple, Devil’s apple, and Duck’s foot; low to the ground with glossy green, drooping, lobed leaves on its few stiff branches, with a pale pink flower and bright red-orange bulbous fruit; propagated by seed or by dividing the rhizome; tolerant to cold temperatures but not to dry conditions. In Eastern Asia, it is found from Afghanistan to China and through the Himalayan ranges.

Many flavonoids and lignans are already known for their antioxidant action and anti-apoptotic potential, and thus contribute towards radioprotection (21). Several mechanisms have been proposed to explain the radiation protection observed, following administration of P. hexandrum extract, such as free radical scavenging, stabilization of mitochondrial cell potential, regulation of cell cycle activities and time dependent apoptosis (12,13,14,15,16,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35).

P. hexandrum exhibited both anti-cancer (pro-oxidant ability) and radioprotective (antioxidant ability) effects respectively depending upon the dose administered (1,20,21,24,29). The pro-oxidant effects are observed in the presence of metal ions by virtue of the presence of some aryltetralin lignans (22), further supporting DNA fragmentation ability at the in vitro level (35). At specific radioprotective doses, it exhibited significant antioxidant effect as summarized in Table 1.

Molecular mechanism of P. hexandrum mediated radioprotection

Cytoprotective properties

We have recently reported that the mode of protection by P. hexandrum at the molecular level includes the modulation of protein expression [associated with cell death (apoptosis) and DNA repair)] by P. hexandrum administration 200 mg/kg.b.wt. i.p. 2 hrs. before 10 Gy irradiation (17,18,19). The most striking observations indicated that as a result of P. hexandrum extract treatment in mice, the expression of heat shock proteins, especially HSP-70 along with its transcriptional factor HSF-1 (heat shock transcription factor; a protein regulates HSP-70 synthesis) was increased significantly as compared to the mice treated with radiation (10 Gy) only. Heat shock proteins are cytoprotective in nature and have been reported to be increased under various environmental stresses such as increased temperature, ionizing radiation and chemical toxicants (17). The overexpression of HSF-1 suggested transcriptional level induction of heat shock proteins in the spleen of mice treated with P. hexandrum extract. The expression of phosphorylating enzymes (proteins regulating phosphate group transfer to other functional proteins) such as PkC, MAPKAP Kinase-2 was also observed to increase in the mice spleen after P. hexandrum treatment (with or without irradiation), as compared to irradiated control suggesting the possible role of phosphorylating enzymes in the signal transduction pathways that is initiated upon P. hexandrum treatment (17,18,19).

Apoptosis inhibitory activities

A strong inhibition of Apoptosis Inducing Factor (AIF - a cell death promoting protein) expression in the group of mice showed overexpression of HSP-70 upon P. hexandrum treatment (17). On the basis of a previous study (36), it was suggested that P. hexandrum treatment initiates an antagonistic interaction between AIF and HSP-70 expression and thus suppresses the apoptotic molecular cascade thereby protecting DNA fragmentation. The anti-apoptotic effect of HSP-70 can be attributed to the ability of P. hexandrum to provide protection to chromatin from proteases and nucleases, which are well known apoptotic markers (17,18,19).

Cell proliferation activities

The role of nuclear factor kappa beta (NFkb) has also been studied extensively in apoptotic regulation NFkb-Ikb complex and was found to be stable in the cytoplasm. However, under radiation stress Ikb2 gets phosphorylated by enzymes like Pkc and consequently free NF-kb moves towards the nucleus, binds with DNA, and initiates a variety of transcription at times leading to induced cell death (37,38). The expression of NF-kb was found to be induced in the cytoplasm upon P. hexandrum treatment (+/- irradiation), but it was found to be translocated into the nucleus. Podophyllum hexandrum treatment inhibited the translocation of free NFkb from the cytoplasm to the nucleus and could explain its anti-inflammatory effects. This effect may have further lead to down-regulation of p53 and up regulation of Bcl-2 protein expression, which may have possible contributions toward reduction of apoptosis and enhanced cell proliferation. Increased expression of Bcl-2, and HSP70, observed following P. hexandrum treatment (+/- irradiation), suggests a role of P. hexandrum in stabilization of the mitochondrial membrane potential leading to inhibition of membrane permeability (36,39). This prevents release of cytochrome C, leading to inhibition of apoptosis and thereby offering protection against radiation-mediated damage to the cells in conformity with the earlier observations (40). The induced expression of Ras-GAP directly demonstrated the activation of Ras-related protein R-Ras in the animals treated with P. hexandrum extract (+/- irradiation), indicating enhanced cell proliferation.

DNA Repair Studies

The expression of proliferating cell nuclear antigen (PCNA), an important cell proliferation marker in the cell system, was found to be enhanced in the spleen of mice treated with P. hexandrum (with or without irradiation), further demonstrating improved cell proliferation and eventually survival. P. hexandrum treatment (with or without irradiation) induced the molecular expression of the Poly (ADP-ribosyl) DNA polymerase (PARP) and down-regulated the expression of caspases and their transcription regulators (i.e., Caspase Activated DNAase), further indicating improved DNA repair and significant inhibition of the apoptosis in the mouse model system (17,18). A summary of the radioprotective action modulated via modulation of expression of proteins is shown in Figure 2.

Figure 3(Click to enlarge)

Figure 2: Possible molecular mechanisms of radioprotection provided by P. hexandrum

Future Prospects

In view of its acceptable therapeutic index and a significant dose-reduction factor, P. hexandrum is a promising candidate plant for development of radioprotective drugs. Since it is an endangered plant, the interesting lead of usage of Trametes hirsuta (an endopyte) for mass production of precursors of radioprotective formulation (41) needs to be further pursued for upscaling. Further studies to characterize the total profile of gene expression (up or down regulation) by cDNA micro-array and the effects of P. hexandrum on protein expression (proteomic profiling) will help unravel the intricate mechanisms of signal transduction pathways operating at the molecular level. Such data will help in the development of novel radioprotectors for human use.


In conclusion, P. hexandrum acts in a holistic manner at various levels. Its administration on mice prior to irradiation leads to a dramatic enhancement (~80%) in survival. At the molecular level, it induces pro-survival protein and DNA repair protein expression while down-regulating the expression of proteins associated with induction of apoptosis. These activities are congruent with the in vitro free radical modulating ability of rhizome extracts of P. hexandrum.


The authors express their sincere thanks to all the past and present workers of radiation biology laboratories of INMAS and Natural Plant Product Division, Regional Research Laboratory, Jammu who have either originated the work quoted in this mini-review or have given them the benefits of their experiences of studies on Podophyllum hexandrum.


Table 1: Radioprotective Studies using Podophyllum hexandrum

Radioprotective Studies

Major Inferences


Survival Study

Serendipitously discovered while evaluating anti-cancerous properties of Podophyllum hexandrum. More than 80% radioprotection observed in a 30-day survival study using Strain ‘A’ Swiss Albino mice against 10 Gy exposure with dose reduction factor of 1.33.

Radioprotective effects of podophyllotoxin, an active constituent of Podophyllum hexandrum were reported in yeast (Sacchromyces cerevisae).

1, 6, 15


The aqueous crude extract (200mg/Kg b.wt., -2hrs) rendered gastroprotection by:

a) threefold increase in number of surviving crypts

b) 2.7-fold increase in villi cellularity

c) limiting the radiation-induced apoptosis in crypt cells

d) modulation of the antioxidant defense system in jejunum and ileum at 12th post-irradiation day

e) enhanced levels of glutathione-S-transferase (GST) and superoxide dismutase (SOD) observed at in vivo level.

1, 36


Sub-lethal (2 Gy) dose was given to rats in utero on day 17 of gestation and pre-irradiation treatment of extract exhibited mitigation of neuro-physiological alternations.

19, 38


In vitro studies, using human hepato carcinoma cell lines further revealed its ability to stabilize the state of mitochondrial oxidative burst, decreased TBARS, time-dependent inhibition of gamma radiation-induced leakage of electrons in the mitochondrial electron transport chain (ETC) via reduction in ROS and NO generation and simultaneous enhancement in the thiol status via neo-synthesis. It also significantly inhibited the radiation-induced enhanced complex I (NADH: UQ reductase) activity. On the other hand, the flow and leakage of electrons from complex I/III (NADH: cytochrome C oxidoreductase) and complex II/III (succinate: cytochrome C oxidoreductase) was maintained. The above studies are in line with modulating ability of extract on antioxidant defense in mice.

20, 21, 30

Reproductive System

Extract administration exhibited significant increases in testis weight, repopulation of the seminiferous tubules and the resting primary spermatocytes and the stem-cell survival index was maintained. Increased levels of sperm counts and reduction in the abnormalities of sperm morphology revealed its ability to protect the testicular system. The extract has also exhibited its ability to modulate antioxidant enzymes in the male reproductive system.

1, 37

Molecular level Investigations

Studies at the molecular level revealed interesting data, e.g., anti-inflammatory activity (reduction of interferon-gamma, interleukin-6 and tumour necrosis factor-alpha secretion in lipopolysaccharide-induced inflammation in isolated macrophages); enhanced MAPKAP (mitogen-activated protein kinase-activated protein) kinase-2 activation along with HSF-1 (heat-shock transcription factor-1) leading to up-regulation of HSP-70 (heat-shock protein-70) with concomitant strong inhibition of AIF (apoptosis-inducing factor) expression; DNA degradation, and translocation of free NF-κβ (nuclear factor kappa beta) from cytoplasm to nucleus leading to decreased expression of tumor suppressor protein p53 and there is a simultaneous increase in Bcl-2 (B-cell chronic lymphocytic lymphoma 2), Ras-GAP (Ras-GTPase-activating protein) and PCNA (proliferating cell nuclear antigen). Such mechanisms have resulted in enhanced survival status.

26, 27, 28

Comparative Studies on Fractionated Extracts of High-Altitude Podophyllum hexandrum and semi-purified extract of Low-altitude Podophyllum hexandrum

On the basis of antioxidant screening using radioprotective studies of Podophyllum hexandrum, aqueous, aqua-alcoholic, chloroform and alcoholic extracts were selected. The polarity of solvent system to be used was established. Further, the comparative analysis with semi-purified extract of low-altitude Podophyllum hexandrum revealed that the semi-purified extract along with alcoholic and chloroform extract exhibited immense potential. The semi-purified extract exhibited significant inhibitory ability against 20 Gy induced double and single strand breaks by virtue of its free radical scavenging potential. The extract acted as a pro-oxidant in the presence of metal ions supported by its DNA fragmentation ability. The extract also exhibited apoptosis induction ability at selected doses. The selected extracts exhibited significant (p<0.05) nitric oxide scavenging potential and antioxidant activity in the lipid phase.

2, 9, 25, 40

Hemopoietic Modulation

The studies are further supported by hemopoietic modulatory ability of the semi-purified extract. The semi-purified extract exhibited significant recovery in hemoglobin content as compared to irradiated group. Total leukocytes content was fairly high on 30th post-treatment day and also the differential leukocyte count was restored to an extent. The activity was found to be attributed to the hydroxyl ion scavenging activity of the extract. The extract prophylactic treatment causes the recovery of the animals on 10th day from bone-marrow aplasia caused due to lethal exposure of gamma radiation (10Gy). In a recent study using a hydro-alcoholic extract of Podophyllum hexandrum, the enhanced expression of heme-oxygenase-1 and pro-survival multi domain Bcl-2 proteins revealed that the extract-induced modulation of hemopoietic system is linked to the expression levels of these proteins. The above studies are in coherence with the immunostimulatory ability and cytoprotective potential of the extract. The extract also exhibited an inherent potential to chelate iron at in vitro level indicating its ability to reduce the amplification process.

5, 14, 16, 24, 35

Role of secondary metabolites of Podophyllum hexandrum in radiation protection


The comparative studies using the comparable levels of aryltetralin lignans exhibited an indicative correlation between the pro-antioxidant behavior of the extracts of Podophyllum hexandrum and the content of individual lignans. The study was just a step towards revealing the role of lignans in radiation protection. In addition, a novel galactoside of quercetin was identified in aquo-alcoholic extract of High-altitude Podophyllum hexandrum and the extract exhibited significant (p<0.05) protein protection and peroxyl radical scavenging activity in ex vivo model. These studies indicated the probable role of polyphenolics in addition to lignans in radiation protection. These leads revealed that the ratio of lignans:polyphenolics might play a critical role in providing overall radiation protection. The endophytic Trametes hirsuta is reported as a novel alternative source of podophyllotoxin and related aryltetralin lignans. An isolated study using endophyte Trametes hirsuta exhibited the independent synthesis of podophyllotoxin and related aryl-tetralin lignans. The isolated lignans, even in combinations of two or more lignans, exhibited significant antioxidant activities relevant to radiation protection. The studies at the compound levels are still in infancy and require augmenting for the development of an effective radioprotective alternative for human use.

10, 11, 33



  1. Arora R, D Gupta, R Chawla, R Sagar, A Sharma, R Kumar, J Prasad, S Singh, N Samanta and RK Sharma (2005) Radioprotection by plant products: Present status and future prospects. Phytotherapy Research 19:1-22.
  2. Jagetia GC (2007). Radioprotective potential of plants and herbs against the effects of ionizing radiation. Journal of Clinical Biochemistry and Nutrition 40:74-81.
  3. Bala M and HC Goel (2004) Radioprotective effect of podophyllotoxin in Saccharomyces cerevisiae. Journal of Environmental Pathology, Toxicology and Oncology 23:139-144.
  4. Cairnie A (1983) Adverse effects of WR-2721. Radiation Research 94: 221-226.
  5. Dorr WF, R Noack, R Spekl, K Farell, (2001) Modification of oral mucositis by keratinocyte growth factor: single radiation exposure. International Journal of Radiation Research 77:341-347.
  6. Kligerman MM, DJ Gloverand AT Turrisi (1984) Toxicity of WR-2721 administered in single and multiple doses. International Journal of Radiation Oncology Biology Physics 10:1773-1776.
  7. Arora R, R Chawla, S Singh, R Kumar, AK Sharma, SC Puri, AK Sinha, RP Tripathi and RK Sharma (2006) Radioprotection by Himalayan High-Altitude Region Plants. In: Herbal Drugs: A Twenty-first Century Perspective, RK Sharma and R Arora (Eds.) Jaypee Brothers Medical Publishing Limited, New Delhi pp. 301-325.
  8. Arora R, R Chawla, S Singh, RK Sagar, R Kumar, A Sharma, J Prasad, S Singh, GU Gurudutta and RK Sharma (2006) Bioprospection for Radioprotective Molecules from Indigenous Plants. In: Recent Progress in Medicinal Plants. Vol 16 - Phytomedicine. JN Govil (Ed.) Studium Press LLC, Houston, Texas, USA pp 179-219.
  9. Patwardhan B, ADB Vaidya and M Chorghade (2004). Ayurveda and natural products drug discovery. Current Science 86:789-799.
  10. Singh J and NC Shah (1994) Podophyllum: a review. Current Research on Medicinal and Aromatic Plants 16:53-83.
  11. Sultan P, AS Shawl, PW Ramteke, A Jan, N Chisti, N Jabeen and S Shabir (2006) In vitro propagation for mass multiplication of Podophyllum hexandrum: a high value medicinal herb. Asian Journal of Plant Sciences 5:179-184.
  12. Goel HC, H Prakash, A Ali and M Bala (2007) Podophyllum hexandrum modulates gamma radiation-induced immunosuppression in Balb/c mice: Implications in radioprotection. Molecular and Cellular Biochemistry 295:93-103.
  13. Goel HC, R Arora and J Prasad (2000) A process for preparation of a radioprotective herbal extract - I and II. Indian Patent filed, Patent Office, New Delhi, India.
  14. Goel HC, R Arora and J Prasad (2001) A process for preparation of a radioprotective herbal formulation. Indian patent filed, Patent Office, New Delhi, India.
  15. Arora R, R Chawla, SC Puri, R Sagar, S Singh, R Kumar, AK Sharma, J Prasad, S Singh, G Kaur, P Chaudhary, GN Qazi and RK Sharma. (2005) Radioprotective and antioxidant properties of low-altitude Podophyllum hexandrum (LAPH). Journal of Environmental Pathology Toxicology and Oncology 24:299-314.
  16. Arora R, R Sagar, S Singh, R Kumar, AK Sharma, J Prasad, S Singh, M Gupta, RK Sharma, SC Puri, B Krishna, MS Siddiqui, SS Lahiri, RP Tripathi and GN Qazi (2007) Cytoprotective effect of Podophyllum hexandrum against gamma radiation is mediated via hemopoietic system stimulation and up-regulation of heme-oxygenase-1 and the prosurvival multidomain protein Bcl-2. Integrative Cancer Therapy 6:54-65.
  17. Kumar R, PK Singh, AK Sharma, J Prasad, RK Sagar, S Singh, R Arora and RK Sharma (2005) Podophyllum hexandrum (Himalayan mayapple) extract provides radioprotection by modulating the expression of proteins associated with apoptosis. Biotechnology and Applied Biochemistry 42: 81-92.
  18. Kumar R, PK Singh, AK Sharma, J Prasad, RK Sagar, S Singh, R Arora and RK Sharma (2005) Radioprotection by Podophyllum hexandrum in the liver of mice: a mechanistic approach. Environmental Toxicology and Pharmacology 20: 326-334.
  19. Kumar R, PK Singh, AK Sharma, J Prasad, RK Sagar, S Singh, R Arora and RK Sharma (2006) Modulation of vital protein expression in intestine of mice by Podophyllum hexandrum: implications in radiation protection. In: Recent Progress in Medicinal Plants. Vol 16 - Phytomedicine. JN Govil (Ed.) Studium Press LLC, Houston, Texas USA pp 236-264.
  20. Chawla R, R Arora, R Kumar, AK Sharma, J Prasad, S Singh, RK Sagar, P Chaudhary, S Shukla, G Kaur, RK Sharma, SC Puri, KL Dhar, G Handa, VK Gupta and GN Qazi (2005) Antioxidant activity of fractionated extracts of rhizomes of high-altitude Podophyllum hexandrum: role in radiation protection. Molecular and Cellular Biochemistry 273:193-208.
  21. Chawla R, R Arora, RK Sagar, S Singh, SC Puri, R Kumar, S Singh, AK Sharma, J Prasad, HA Khan, RK Sharma, KL Dhar, M Spiteller and GN Qazi (2005) 3-O-beta-D-Galactopyranoside of quercetin as an active principle from high altitude Podophyllum hexandrum and evaluation of its radioprotective properties. Zeitschrift fur Naturforschung - Section C [Journal of Biosciences (C)] 60:728-38.
  22. Chawla R, R Arora, S Singh, RK Sagar, RK Sharma, R Kumar, A Sharma, RP Tripathi, SC Puri, HA Khan, AS Shawl, P Sultan, T Krishan and GN Qazi (2006) Podophyllum hexandrum offers Radioprotection by Modulating Free Radical Flux: Role of Aryl-Tetralin Lignans. Evidence Based Complementary and Alternative Medicine 3:503-11.
  23. Goel HC, PK Agrawala, V Pathania, N Malhotra (2003). Immunomodulatory and cytoprotective role of RP-1 in g-irradiated mice. Molecular and Cellular Biochemistry 254:73-81.
  24. Goel HC, J Prasad, A Sharma and B Singh (1998) Antitumour and radioprotective action of Podophyllum hexandrum. Indian Journal of Experimental Biology 36:583-587.
  25. Goel HC, S Sajikumar and A Sharma (2002) Effects of Podophyllum hexandrum on radiation induced delay of postnatal appearance of reflexes and physiological markers in rats irradiated in utero. Phytomedicine 9:447-454.
  26. Gupta D, R Arora, AP Garg and HC Goel (2003) Radiation protection of HepG2 cells by Podophyllum hexandrum royale. Molecular and Cellular Biochemistry 250:27-40.
  27. Gupta D, R Arora, AP Garg, M Bala and HC Goel (2004) Modification of radiation damage to mitochondrial system in vivo by Podophyllum hexandrum: Mechanistic aspects. Molecular and Cellular Biochemistry 266:65-77.
  28. Kumar IP and HC Goel (2000) Iron chelation and related properties of Podophyllum hexandrum, a possible role in radioprotection. Indian Journal of Experimental Biology 38:1003-1006.
  29. Kumar IP, SVS Rana, N Samanta and HC Goel (2003) Enhancement of radiation-induced apoptosis by Podophyllum hexandrum. Journal of Pharmacy and Pharmacology 55:1267-1273.
  30. Mittal A, V Pathania, PK Agrawala, J Prasad, S Singh, and HC Goel (2001) Influence of Podophyllum hexandrum on endogenous antioxidant defence system in mice: Possible role in radioprotection. Journal of Ethnopharmacology 76:253-262.
  31. Sagar RK, R Chawla, R Arora, S Singh, B Krishna, RK Sharma, SC Puri, P Singh, R Kumar, AK Sharma, S Singh, J Prasad, B Gupta, B Ahmed, KL Dhar, HA Khan, ML Gupta and GN Qazi (2006) Protection of hematopoietic system by Podophyllum hexandrum. Planta Medica 72:114-120.
  32. Salin CA, N Samanta and HC Goel (2001) Protection of mouse jejunum against lethal irradiation by Podophyllum hexandrum. Phytomedicine 8:413-422.
  33. Samanta N, K Kannan, M Bala, HC Goel (2004) Radioprotective mechanism of Podophyllum hexandrum during spermatogenesis. Molecular and Cellular Biochemistry 267:167-176.
  34. Sajikumar S and HC Goel (2003) Podophyllum hexandrum prevents radiation-induced neuronal damage in postnatal rats exposed in utero. Phytotherapy Research 17:761-766.
  35. Shukla SK, P Choudhary, IP Kumar, F Afrin, SC Puri, GN Qazi and RK Sharma (2006) Radiomodifying effects of a fractionated extract of Podophyllum hexandrum: A mechanistic study. Environmental Toxicology and Pharmacology. 22:113-120.
  36. Ravagnan L, S Gurbuxani, SA Susin, C Maisse, E Daugas, N Zamzami, T Mak, M Jaattela, JM Penninger, C Garrido and G Kroemer (2001) Heat shock protein 70 antagonizes apoptosis-inducing factor. Nature Cell Biology 3:839-843.
  37. Brach MA, R Hass, ML Sherman, H Gunji, R Weichselbaun and K Donald (1991) Ionizing radiation induces expression and binding activity of nuclear factor kB. Journal of Clinical Investigation 88:691-695.
  38. Mercurio F and AM Manning (1999) NFkB as a primary regulator of the stress response. Oncogene 18: 6163-6171.
  39. Nylandsted J, M Rohde, K Brand, L Bastholm, F Elling and M Jaattela (2000) Selective depletion of heat shock protein 70 activates a tumour-specific death program that is dependent of caspases and bypass Bcl-2. Proceeding of the National Academy of Sciences, USA 97(14):7871-7876.
  40. Gilbert MS, AH Saad, BA Rupnow and SJ Knox (1996) Association of Bcl-2 with membrane hyperpolarization and radioresistance. Journal of Cell Physiology 86(11): 5593-5599.
  41. Puri SC, A Nazir, R Chawla, R Arora, S Riyaz-ul-Hassan, T Amna, B Ahmed, V Verma, S Singh, RK Sagar, AK Sharma, R Kumar, RK Sharma and GN Qazi (2006) The endophytic Trametes hirsuta as a novel alternative source of podophyllotoxin and related aryl tetralin lignans. Journal of Biotechnology 122:494-510.

View this Article by:
Print PDF | Discussion (0 comments)

Add Comment

 Copyright © 2024 Trees for Life Journal
 All trademarks and copyrights on this page are owned by their respective owners.

Powered By Geeklog