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Year : 2013  |  Volume : 34  |  Issue : 2  |  Page : 215-219  

Effect of Drakshavaleha in cyclophosphamide induced weight loss and reduction in crown-rump length in developing mice embryo

1 Associate Professor Department of Sharira Rachana, National Institute of Ayurveda, Jaipur, India
2 Prof of Anatomy and Ex. Director, Institute of Medical Sciences, BHU, Varanasi, India
3 Associate Prof. Department of Rasashastra, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India

Date of Web Publication10-Oct-2013

Correspondence Address:
Sunil Kumar
Associate Professor, Department of Sharira Rachana, National Institute of Ayurveda, Jaipur - 302 002, Rajasthan
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0974-8520.119686

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Being an anti-mitotic and apoptosis inducing agent, Cyclophosphamide (CP) causes stunting in size and loss of body weight of the pups on intra-peritoneal injection (10 mg/kg) to pregnant mice on day 11 of gestation. Loss of body weight due to CP administration could be minimized by feeding Drakshavaleha (16 g/kg) orally to pregnant mice from day "0" to day "18" of their gestation. Recovery observed in terms of body weight of the pups was statistically significant (P < 0.001) in Drakshavaleha treated pups. Drakshavaleha also recovered the crown-rump length of the pups occurred due to CP administration. Growth retardation with decreased fetal weight was observed in all CP treated pups when compared with the controls.

Keywords: Cyclophosphamide, Drakshavaleha, mice, Rasayana, vitamins, weight-loss

How to cite this article:
Kumar S, Singh G, Reddy K. Effect of Drakshavaleha in cyclophosphamide induced weight loss and reduction in crown-rump length in developing mice embryo. AYU 2013;34:215-9

How to cite this URL:
Kumar S, Singh G, Reddy K. Effect of Drakshavaleha in cyclophosphamide induced weight loss and reduction in crown-rump length in developing mice embryo. AYU [serial online] 2013 [cited 2023 May 31];34:215-9. Available from: https://www.ayujournal.org/text.asp?2013/34/2/215/119686

   Introduction Top

Programmed cell death is a part of normal development of an individual during his intra-uterine life. Altered rate of programmed cell death at a critical period of development may lead to serious structural defects. Likewise, altered rate of cell proliferation may also induce malformations. [1] Thus agents that interfere with the cell proliferation or differentiation cause congenital malformations. Cyclophosphamide (CP) is one of such agents.

Rasayana therapy is one of the eight branches of Ayurveda, constitute a group of single or polyherbal preparations made from plant extracts, commonly used to improve health and longevity. It has been reported that Rasayanas have immunomodulatory, anti-oxidant and anti-tumor functions improve memory, intelligence, youthfulness, luster, complexion, and efficiency. [2] It helps to preserve harmony in three psychobiological dimensions known as Doshas[3] and biological rhythms, which regulate the entire functioning of the physiology. [4] Drakshavaleha has been indicated to treat Pandu (anemia) and Kamala (jaundice). [5] Due to anti-anemic properties and nutritional values, it has been used as a Naimittika Rasayana (promoter of specific vitality in specific disease) by some of the Ayurvedic physicians in Rajasthan to a woman during her pregnancy expecting a good health of both mother and her offspring.

Prenatal supplementation with multiple micronutrients has a greater positive impact on birth weight than supplementation with iron/folic acid. [6] Keeping this fact in mind, the objective of the study was to investigate the protective effect of Drakshavaleha against CP induced growth retardation in mice pups in terms of body weight and crown-rump (CR) length. As most of the teratogens act by causing hypoxia, the protecting nature of the Drakshavaleha may neutralize their damaging effects by its Rasayana functions (oxygenating/anti-oxidant nature).

   Materials and Methods Top

Avaleha or Leha intended for internal administration is a semi solid preparation of drugs by addition of Sharkara (sugar), decoctions, juices, etc., Its acceptance is more as compared to other classical Ayurvedic drugs. Drakshavaleha (one such Avalehas) used in the study was prepared as per the procedure of the Avaleha Kalpana.[7]

Ethical guidelines for use and care of laboratory animals were followed as per the guidelines of Indian Council of Medical Research, New Delhi ICMR. [8] Eighty mice (40 male and 40 female) with an average age of 50 days weighing 25 ± 5 g used in the study were procured. All mice were kept in isolation for 19 days to confirm that they are non-pregnant and had a normal estrous cycle. Mice found in proestrous phase of the cycle were caged with normal males of the same strain overnight in an air cooled room at 75°F with 50% humidity. Animals were provided standard food pellets and tap water 'ad libitum' throughout the study. Mating was accomplished by placing one male and one female mouse in the polypropylene cage. Vaginal smear of the female mice were examined for spermatozoa at 8 a.m. next morning. Mating was confirmed by the presence of sperms in the vaginal smear. Mid night of the day of mating was designated as day "0" of the embryo development and subsequent 24 h period was considered as day "1" of the gestation. Sperm positive females were isolated and divided into the following groups:

Group I (Control): Pregnant mice (n = 10) received 0.2 ml of vehicle (distilled water) intra-peritoneal on day 11 of pregnancy. Group II (Drakshavaleha): Pregnant mice (n = 10) received Drakshavaleha (16 g/kg) orally from day "0" to day "18" of pregnancy. Group III (CP): Pregnant mice (n = 10) received CP (10 mg/kg) intra-peritoneal on day 11 of pregnancy. Group IV (CP + Drakshavaleha) : Pregnant mice (n = 10) received CP (10 mg/kg) intra-peritoneal on day 11 under cover of Drakshavaleha (16 g/kg) orally from day "0" to day "18" of pregnancy [Table 1].
Table 1: Grouping of the animals and posology

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On day 19 of pregnancy i.e., 1 day prior to full term (20 days) mice were put under ether anesthesia and hysterectomy was done. The uterine sacs were inspected and recorded for sites of resumptions and viable fetuses. The fetuses were removed from the uterus and dried by wiping on a blotting paper. Every pup was weighed and measured (CR length) with the help of weighing machine (least count of 10 mg) and slide Vernier caliper respectively. These pups were examined under magnifying lens and dissecting microscope for external malformations.

Dose of Drakshavaleha was 16 g/kg body weight. CP manufactured by Biochem Pharmaceutical Industries Ltd, Mumbai, India with a trade name of "Inj. Cycloxan" was used in the experiment.

Statistical analysis

All the results expressed as mean ± Standard Deviation SD intergroup comparisons have been done by one way ANOVA followed by Post-hoc test Statistical Package for the Social Sciences (SPSS, Version 13).

   Observations and Results Top

As seen in [Table 2], the pups which were administered after Drakshavaleha throughout the period of gestation, average weight was 1.27 ± 0.10 g (93 pups) as against controls which had weight of 1.17 ± 0.17 g (67 pups). Its statistical correlation was highly significant (P < 0.001). The comparison was suggestive of significant gain of the weight of pups following Drakshavaleha administration to the mother mice. The CR length was also of same conclusion i.e., 2.47 ± 0.12 cm versus 2.35 ± 0.16 cm in the Drakshavaleha and controls respectively [Table 3]. It was therefore concluded beyond doubt that Drakshavaleha increases size and weight of pups born to mothers who were fed Drakshavaleha during pregnancy. In CP group these two observations (weight and CR length) showed a significant decrease i.e., 0.84 ± 0.20 g (61 pups) and 1.97 ± 0.22 cm as compared with controls in which mean weight and CR length was 1.17 ± 0.17 g (67 pups) and 2.35 ± 0.16 cm respectively. The difference between two groups, i.e., CP versus control shows a significant decrease in size of pups (P < 0.001). In the group where mother mice were administered CP undercover of Drakshavaleha (group IV) the loss in the weight and size of the pups showed a significant recovery (P < 0.001). However, size remained smaller as compared with controls and animals fed with Drakshavaleha alone. The average weight of the pups of CP + Drakshavaleha group was 1.00 ± 0.16 g versus control and Drakshavaleha alone group, i.e., 1.17 ± 0.17 g and 1.27 ± 0.10 g respectively. The CR length showed recovery from an average of 1.97 ± 0.22 cm in CP group to 2.24 ± 0.18 cm in CP + Drakshavaleha group [Figure 1]. Though, there is obvious recovery from the CP group, the weight and size still remained smaller as compared to controls and Drakshavaleha groups.
Table 2: Effect of Drakshavaleha on weight of pups

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Table 3: Effect of Drakshavaleha on crown-rump length of pups

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Figure 1: Pups of mice collected on day 19 of pregnancy. (a) Treated with cyclophosphamide (CP) (10 mg/kg on 11th day) showing the crown-rump length as compared with (b) Treated with both CP (10 mg/kg, 11th day) under cover of Drakshavaleha (16 g/kg, 0-18 days)

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In the present investigation, the effect of CP causing growth retardation and decreased fetal weight were seen [Table 3], [Graph 1] [Additional file 1] when the drug was injected on 11 th day of gestation in CP group. Among litters whose mothers received the drug (CP) on the same day in same dose under Drakshavaleha cover (group IV) the pups were seen with significant weight gain, which however, was lower as compared to the pups born to mothers with administration of Drakshavaleha alone (group II). CR length was also of same conclusion, i.e. 2.47 ± 0.12 versus 2.35 ± 0.16 cm in group II and group I respectively [Graph 2]. [Additional file 2] The above observation suggests that Drakshavaleha (alone) increases the size and weight of pups when given to mother mice during gestation period and the difference between the two groups is statistically significant (P < 0.001).

   Discussion Top

CP is known to reduce fetal weight drastically and is an established teratogen. This reduction of weight is due to intensive anti-mitotic activity of CP. It also increases the rate of apoptosis. Teratogenic doses of CP on day 11 after copulation is associated with a dose-related increase in embryo lethality, gross morphological abnormality and cephalic Deoxyribonucleic acid DNA strand breaks and a reduction in fetal weight DNA is the primary target of embryo-toxic mechanism of CP. [9]

The precise reasons for the protective effects of Drakshavaleha against any teratogen induced malformation are not clear till date however, the possibilities can be considered.

Multivitamin supplementation use among pregnant women is as effective as iron-folic acid in improving anemia status and appears to have other benefits for maternal and child nutritional status. [10] Ascorbic acid (vitamin C) is an important intracellular reducing agent. Its anti-oxidant properties protect against the adverse effects of free radicals reactions. Ascorbate inhibits CP induced sister-chromatids exchanges in mice. [11] Vitamin C supplementation may help to reduce the risk of pregnancy complications like pre-eclampsia, intrauterine growth restriction and maternal anemia. [12] Vitamin P enhances the action of vitamin C and for this reason they should be taken together. (Rhyme for ancient wanderer.) Large, transient increases in the total anti-oxidant capacity of plasma have often been observed after the consumption of flavonoid rich foods by humans. [13] Vitamins and minerals referred to collectively as micronutrients have important influences on the health of pregnant women and the growing fetus. [14] To prevent teratogen induced DNA damage, optimum dose of vitamins is required to be given during their intra-uterine life than more doses of the vitamins.

By Ayurvedic concept of physiology, it may be presumed that a Rasayana agent promotes nutrition through one of the following modes: [15] (a) By direct enrichment of the nutritional quality of Poshaka Rasa, i.e., the nutrient plasma. (b) By promoting nutrition through improving the Agnivyapara i.e., digestion and metabolism. In general, all Rasayanas are nutrition promoters but some are specific to certain organs or diseases called Naimittika Rasayana, [16] for example, Hridaya Rasayana for heart, Twachya Rasayanas for skin, Chaksusya Rasayanas for eyes and others. Due to rich in nutritional values and iron supplements Drakshavaleha can been used as a Naimittika Rasayanas pregnancy which may help to promote the health of the pregnant women and facilitates full growth and development of progeny in the womb.

   Conclusion Top

In the present context, Drakshavaleha [Table 4] can be conceived to be a Naimittika Rasayana during pregnancy to obtain a healthy progeny. Whether a single ingredient of Drakshavaleha such as vitamin C, vitamin P, folic acid, minerals, etc., was effective in the current research or the result was a collective outcome is such difficult to conclude at this level. Rasayana as a whole has been the approach by Ayurveda and the current research follows this trend while being less analytical.
Table 4: Formulation composition of Drakshavaleha

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   References Top

1.Diamantis A, Magiorkinis E, Sakorafas GH, Androutsos G. A brief history of apoptosis: From ancient to modern times. Onkologie 2008;31:702-6.  Back to cited text no. 1
2.Mohandas Rao KG, Muddanna Rao S, Gurumadhva Rao S. Centella asiatica (L.) leaf extract treatment during the growth spurt period enhances hippocampal CA3 neuronal dendritic arborization in rats. Evid Based Complement Alternat Med 2006;3:349-57.  Back to cited text no. 2
3.Patwardhan B, Warude D, Pushpangadan P, Bhatt N. Ayurveda and traditional Chinese medicine: A comparative overview. Evid Based Complement Alternat Med 2005;2:465-73.  Back to cited text no. 3
4.Joshi H, Parle M. Brahmi rasayana improves learning and memory in mice. Evid Based Complement Alternat Med 2006;3:79-85.  Back to cited text no. 4
5.Vagbhatta, Astanga Hridayam, Chikitsa Sthan 16/29. In: Murthy KR, editor. 1 st ed. Varanasi: Krishnadas Academy; 1992. p. 451.  Back to cited text no. 5
6.Zagré NM, Desplats G, Adou P, Mamadoultaibou A, Aguayo VM. Prenatal multiple micronutrient supplementation has greater impact on birthweight than supplementation with iron and folic acid: A cluster-randomized, double-blind, controlled programmatic study in rural Niger. Food Nutr Bull 2007;28:317-27.  Back to cited text no. 6
7.Sharangadhara, Sharangadhara Samhita Madhyama Khanda, 8/1. In: Tripathi B, editor. 1 st ed. Varanasi: Chaukhambha Surbharati Prakashan; 2007. p. 210.  Back to cited text no. 7
8.ICMR guidelines, Available from: http://www.icmr.nic.in/ethical_guidelines.pdf. [Last accessed on 2010 Dec 10].  Back to cited text no. 8
9.Pillans PI, Ponzi SF, Parker MI. Effects of ascorbic acid on the mouse embryo and on cyclophosphamide-induced cephalic DNA strand breaks in vivo. Arch Toxicol 1990;64:423-5.  Back to cited text no. 9
10.Sunawang, Utomo B, Hidayat A, Kusharisupeni, Subarkah. Preventing low birthweight through maternal multiple micronutrient supplementation: A cluster-randomized, controlled trial in Indramayu, West Java. Food Nutr Bull 2009;30:S488-95.  Back to cited text no. 10
11.Krishna G, Nath J, Ong T. Inhibition of cyclophosphamide and mitomycin C-induced sister chromatid exchanges in mice by vitamin C. Cancer Res 1986;46:2670-74.  Back to cited text no. 11
12.Rumbold A, Crowther CA. Vitamin C supplementation in pregnancy. Cochrane Database Syst Rev 2005;2CD004072.  Back to cited text no. 12
13.Lotito SB, Frei B. Consumption of flavonoid-rich foods and increased plasma antioxidant capacity in humans: Cause, consequence, or epiphenomenon? Free Radic Biol Med 2006;41:1727-46.  Back to cited text no. 13
14.Black RE. Micronutrients in pregnancy. Br J Nutr 2001;85:S193-7.  Back to cited text no. 14
15.Singh RH. Positive health potentials of Rasayan-Vajikaran therapy in Ayurveda. Bangalore: Ayurmedline. 2000; 2,1-9.  Back to cited text no. 15
16.Dalhan, Susruta Samhita, Chikitsa Sthana 27/12. In: Shastry A. 11 th ed. Varanasi: Chaukhamba Sanskrit Sansthan; 1997.  Back to cited text no. 16


  [Figure 1]

  [Table 1], [Table 2], [Table 3], [Table 4]

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