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PHARMACOLOGICAL RESEARCH
Year : 2011  |  Volume : 32  |  Issue : 2  |  Page : 275-278  

Immunomodulatory activity of Vachadhatryadi Avaleha in albino rats


1 Assistant Professor, Department of Kaumarabhritya, Institute for Post Graduate Teaching and Research in Ayurveda, Gujarat Ayurved University, Jamnagar, Gujarat, India
2 Research Assistant, Pharmacology Laboratory, Institute for Post Graduate Teaching and Research in Ayurveda, Gujarat Ayurved University, Jamnagar, Gujarat, India
3 Ex.Head, Pharmacology Laboratory, Institute for Post Graduate Teaching and Research in Ayurveda, Gujarat Ayurved University, Jamnagar, Gujarat, India

Date of Web Publication2-Feb-2012

Correspondence Address:
S Rajagopala
Department of Kaumarabhritya, Institute for Post Graduate Teaching and Research in Ayurveda, Gujarat Ayurved University, Jamnagar - 361 008, Gujarat
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-8520.92546

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   Abstract 

The present study is carried out to evaluate the immuno-modulatory activity of Vacha Dhatryadi Avaleha in albino rats. Vacha Dhatryadi Avaleha was prepared by classical method and evaluated for humoral antibody formation and cell-medicated immunity in established experimental models. Test formulation was administered at the dose of 900 mg/kg and parameters like hemagglutination titer, ponderal changes, histopathology of immunological organs and immunological paw edema were recorded. Vacha Dhatryadi Avaleha significantly enhanced antibody formation and moderately suppressed the immunological edema. The present study concludes that Vachadhatryadi Avaleha has immunopotentiating activity.

Keywords: Cell mediated immunity, hemagglutination titer, Vachadhatryadi


How to cite this article:
Rajagopala S, Ashok B K, Ravishankar B. Immunomodulatory activity of Vachadhatryadi Avaleha in albino rats. AYU 2011;32:275-8

How to cite this URL:
Rajagopala S, Ashok B K, Ravishankar B. Immunomodulatory activity of Vachadhatryadi Avaleha in albino rats. AYU [serial online] 2011 [cited 2019 Jul 23];32:275-8. Available from: http://www.ayujournal.org/text.asp?2011/32/2/275/92546


   Introduction Top


Ayurveda is the art and science of life, and is one of the richest heritages gifted to mankind by our great ancestors. One of the main strategies in Ayurvedic medicine is to increase body's natural resistance to the disease-causing agent rather than directly neutralizing the agent itself in practice. Ayurveda has propounded the concept of immunity as "Vyadhikshamatwa".[1]

The use of herbs for improving the overall resistance of body against common infections and pathogens has been a guiding principle of Ayurveda [2] and for this there is a separate class of immunomodulatory drugs known as Rasayanas. [3],[4],[5],[6] They are supposed to have the ability of protecting the body against external factors that induce disease. This implied resistance against disease may represent the modern concept of immunity. [7]

Prakara Yoga (indigenous method or practice of enhancing body immunity) narrated in the 35 th chapter of text Arogya Raksha Kalpadrumam,[8] in which the drug schedule starts with birth and continues to the age of 12 years for the purpose of enhancing non-specific immunity of the body. In whole regimen of Prakara Yoga, good numbers of drugs are used at various developmental stages in which some drugs were found to be repeated at almost every level. The drugs which are used several times in this schedule and which are reported to have immunomodulatory activity were selected and a Avaleha (Confection) form was prepared for the clinical trials on children (Avaleha formulation being ideal for administration in children as the question of palatability and acceptability are made easier). Thus prepared formulation was subjected to pharmacological screening in experimental models of immunomodulatory activity to provide experimental basis to clinical findings.

Test formulations

Vachadhatryadi Avaleha contains Vacha (Acorus calamus Linn.), Dhatri (Emblica officinalis Garten.), Musta (Cyperus rotundus Linn), Pushkaramula (Inula racemosa Hook.), Jeeraka (Cuminum cyminum Linn.), Shankhapushpi (Convolvulus pluricaulis Chois.), Pippali (Piper longum Linn.), Sita (sugar), Kshaudra (honey), Sarpi (ghee) and Trikatu (three pungent drugs viz. powders of Shunti (Zingiber officinale Roxb), Maricha (Piper nigrum Linn.) and Pippali (Piper longum Linn.). [9] The combination was named after the first drug of the combination as Vachadhatryadi Avaleha.

The Adjuvant Yoga comprised the following drugs except the herbal drugs of the Vachadhatryadi Avaleha i.e., Kshaudra (honey), Sarpi (ghee), Sita (sugar) and Trikatu as Prakeshepa. This combination is formulated in order to elicit the action of the drugs under trial or to separate the action of Sita, Kshaudra and Sarpi, which are used as media for the preparation of Avaleha in Vachadhatryadi Avaleha formulaiton.

These two formulations (Avaleha) were prepared in Pharmacy attached to the institute as per classical procedures [10] and stored in an air tight container for experimental purposes.

Animals

Charles Foster strain albino rats of either sex weighing between180 ± 30g were selected from the animal house attached to the institute. They were housed at 22 ± 03°C with constant humidity of 50-70% on a 12 h natural day and night cycles. They were fed with diet Amrut brand rat pellet food supplied by Pranav Agro Industries, Baroda and tap water was given ad libitum. The experiments were carried out in accordance of the Institutional animal ethics committee after obtaining its permission.

Dose selection and schedule

The classical dose of Vachadhatryadi Avaleha is 10 g/day. [10] The dose for experimental animals was calculated by extrapolating the human dose to animals (900 mg/kg) based on the body surface area ratio by referring to the standard table of Paget and Barnes. [11] The drug solutions were made with distilled water (90mg/ml) and administered to animals in the dose of 1 ml/100 g body weight with the help of gastric catheter sleeved to syringe. The drugs were administered to overnight fasted animals.

Effect on humoral antibody formation

The effect of test drugs on anti-body formation against sheep red blood cells (SRBC) was studied as described by Puri et al. [12] The selected animals were divided into three groups. First group received distilled water and served as the control group. Second group received Vachadhatryadi Avaleha and third group received Adjuvant Yoga. The drugs were administered for 10 consecutive days. On third day, sheep blood was collected from the city slaughter house in a sterilized bottle containing Alsever's solution (2% dextrose, 0.8% sodium citrate, 0.5% citric acid and 0.42% sodium chloride) aseptically so that agglutination of blood does not take place. The collected sheep blood was thoroughly washed with sterile normal saline through repeated centrifugation until the supernatant fluid became colorless and made to 30% SRBC solution. This sensitizing agent was injected subcutaneously in the dose of 0.5 ml/100 g of body weight to the rats.

On the eleventh day, the animals were sacrificed by ether over dose and the blood was collected in sterile test tubes. Serum was separated from it and complement in it was inactivated by incubating it for 30 min at 56°C temperature in a serological water bath.

Estimation of antibody titer

The micro-titer plate was filled with 0.1 ml sterile normal saline and serial two fold dilutions of 0.1 ml of the serum in sterile saline solution were made in the micro-titer plate up to 16 times. 0.1 ml of thrice saline washed with 3% SRBC was added to each well of the tray. Blood from the same animal (sheep) was used for both sensitization and to determine antibody titer. The trays were covered and placed in refrigerator overnight. Antibody titer (hemagglutination titer) was noted on the next day. The titer was converted to log 2 values for easy comparison. [13]

Spleen, thymus and lymph nodes were dissected out from the animals and their weight was recorded. Tissues were transferred to 10% formaldehyde solution for fixation and the histopathological slides were prepared by referring standard procedure. [14] The slides were viewed under binocular research Carl-Zeiss's microscope (Germany) at various magnifications to note down the changes in the microscopic features of the tissues studied.

Effect on cell-mediated immunity

Effect on cell-mediated immunity was evaluated by following the procedure of Bhattacharya. [15] First group received distilled water and served as the control group. Second group received Vachadhatryadi Avaleha and third group received Adjuvant Yoga. All the animals were sensitized subcutaneously (0.5 ml/100 g body weight) on first day of drug administration by following solution; triple antigen (DPT) - 1ml, normal saline (0.9%) -4 ml and potash alum (10%) - 1 ml. The pH of the above solution was maintained between 5.6 and 6.8 using 10% sodium carbonate. The drug administration was continued for seven consecutive days. On the seventh day, 1 h after drug administration the initial paw volume of left hind paw was noted and 0.1 ml of above solution was injected into plantar aponeurosis of same paw. Volume of immunological edema thus produced was measured by volume displacement method [16] after 24 h and 48 h of injection with plethysmograph. Percentage increase in paw volume, which is the index of edema formation over initial value, was calculated. The values from control group were compared with the values from test and adjuvant drug administered groups to assess the cell-mediated immunity response of the drugs.

Statistical analysis

Results were presented as Mean ± SEM, difference between the groups was statistically determined by unpaired Student's 't' test [17] with the level of significance set at P<0.05. The level of significance was noted and interpreted accordingly.


   Results Top


The data on the effect of test drugs on body weight gain changes in experimental animals are shown in [Table 1]. In comparison to the control group where the percentage increase of body weight was 19.63%, the rate of increase in body weight was less in Vachadhatryadi Avaleha (8.33%) and Adjuvant Yoga (13.93%) treated groups. The decreased rate of body weight gain observed in Vachadhatryadi group was found to be statistically significant (P< 0.001) in comparison to body weight gain in control group.
Table 1: Effect of Vachadhatryadi Avaleha and Adjuvant Yoga on ponderal changes in SRBC sensitized rats

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Both Vachadhatryadi Avaleha and Adjuvant Yoga significantly (***P< 0.001) enhanced antibody titer [Table 2] in comparison to control group, the percentage of increase in Adjuvant Yoga (29.39%) was comparatively less as compared to the Vachadhatryadi Avaleha treated group (32.32%).
Table 2: Effect of Vachadhatryadi Avaleha and adjuvant Yoga on hemagglutination titer in SRBC pre-sensitized rats

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The data on the effect of test drugs on triple antigen induced immunological edema have been presented in [Table 3]. In Vachadhatryadi Avaleha administered group an apparent but statistically non-significant decrease in the paw volume was observed with respect to both 24 and 48 h recordings. In Adjuvant Yoga administered group no apparent effect was observed.
Table 3: Effect of Vachadhatryadi Avaleha and adjuvant Yoga on immunological paw edema in triple antigen sensitized rats

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   Discussion Top


A normal immune system develops through the interaction of many cellular and humoral components that develop at different rates during fetal and early postnatal life. [18] The main objective of Rasayana therapy is to equip the body in such a manner that it is toned up to combat its exposure to adverse conditions. The main mechanism is to enhance different body defense mechanisms in a non-specific manner to endow it with better capacity to get adapted to different kinds of adverse conditions. [19] Among these effects is the enhancement of immune responsiveness of an organism against a pathogen by non-specifically activating the immune system using immunomodulating agents of plant origin.

Vachadhatryadi Avaleha and Adjuvant Yoga significantly (P<0.001) increased the antibody titer. This clearly shows that adjuvant Yoga (viz. comprised of Kshaudra (honey), Sarpi (ghee), Sita (sugar) and Trikatu as Prakshepa) per se have anti-body enhancing effect [P<0.001; [Table 2]]. Combining adjuvant with primary drugs leads to further moderate increase in anti-body formation. In comparison to control group, adjuvant-administered group shows significant enhancement in anti-body titer (29.39%) and combination of Vacha, Dhatri, Musta, Pushkaramula etc. drugs with adjuvant further enhanced the anti-body formation (32.32%) [Table 2]. The possible stages for this can be accelerated processing of antigen by the macrophages, enhanced secretion of cytokines like IL- 4 and tissue growth factor-b (TGB-b) both of which stimulate B-lymphocytes to proliferate. [20] The other possible mechanisms can be enhanced response to the effect of cytokines released during the induction and proliferative phases possibly through up-regulation of the receptors involved, modulation of cytokine gene expression. Further both the formulations did not have any significant influence on the ponderal and histopathology of organs related to immune system.

Vachadhatryadi Avaleha decreased the immunological paw edema both at 24 and 48 h which indicates that the formulation has only weak to moderate CMI suppression effect. Adjuvant Yoga did not produce any desirable effect on the CMI.

Many of the drugs used in this formulations are reported to have immune-modulatory activity; viz., Vacha,[21] Dhatri,[22],[23],[24] Musta,[25],[26] Pushkaramula,[27] Pippali,[28],[29] Shunti[30] and Maricha.[31] Further, the immune-potentiating properties of Madhu[32],[33],[34] and Ghrita[35],[36] are also well established. Thus, the observed activity may be attributed to one or more bioactive principles present in these drugs. From this study, it can be concluded that the Vachadhatryadi Avaleha has immunopotentiating activity and can be used to enhance the immune system in children.


   Acknowledgments Top


Authors are thankful to Director, IPGT and RA, Gujarat Ayurved University, Jamnagar for providing essential technical and financial support for this study.

 
   References Top

1.Agnivesha, Charaka Samhita, commentary by Chakrapani 'ayurveda Dipika', edited by Vaidya Jadavaji Trikamji Acharya, Chaukhambha Sanskrit Sansthan. Varanasi: reprint 2004, Sutrasthana, chapter 28, shloka 07.  Back to cited text no. 1
    
2.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. 2
[PUBMED]  [FULLTEXT]  
3.Bhattacharyaa SK, Muruganandam AV. Adaptogenic activity of Withania somnifera - an experimental study using a rat model of chronic stress. Pharmacol Biochem Behav 2003;75: 547-55.  Back to cited text no. 3
    
4.Agnivesha, Charaka Samhita, commentary by Chakrapani 'ayurveda Dipika', edited by Vaidya Jadavaji Trikamji Acharya, Chaukhambha Sanskrit Sansthan. Varanasi: reprint 2004, Chikitsasthana, chapter 01, shloka 1/4, 1/7-8, 1/23, 4/6.  Back to cited text no. 4
    
5.Sushruta, sushtura Samhita, commentary by Sri Dalhanacharya 'Nibandhasangraha', chaukhambha Orientalia. chapter 27 and 30. 8 th ed. Varanasi, India: Chikitsasthana; 2005.  Back to cited text no. 5
    
6.Vahata, Astangasamgraha, commentary by Indu, 'sasilekha', Chowkhamba Sanskrit series office. Varanasi, India: Uttara Tantra; chapter 49, shloka 1, 2.   Back to cited text no. 6
    
7.Singh RH, Udupa KN. Clinical and experimental studies on Rasayana drugs and Rasayana therapy. In: Bhattacharyaa SK, Muruganandam AV,editor. Adaptogenic activity of Withania somnifera - an experimental study using a rat model of chronic stress. Pharmacol Biochem Behav 2003;75:547-55.  Back to cited text no. 7
    
8.Kaikulangara Variath Rama Varier. 'Arogyarakshakalpadrumam'. Chapter 35. In: Vaidya KS, editor. Kollam: Gopalan Pillai; 1946.  Back to cited text no. 8
    
9.Sri Bhavamishra, 'Bhavaprakasha Nighantu'. commentary by Chunekar KC. Varansi, India: Chaukhambha Bharati Academy; 2006. P.11,13,14,16,17,19,31,43,80,94,95,243,342,454.  Back to cited text no. 9
    
10.Sharangadhara. 'Sharangadhara Samhita', commentaries by Aadhamalla 'Dipika' and Kashiram 'Gudartha- Dipika'. 4 th ed. Choukhambha Orientalia. Varanasi, India: Prathama Khanda; 2000, chapter 8, Shloka 01-04.  Back to cited text no. 10
    
11.Paget GE, Barnes JM. Evaluation of drug activities. In: Lawrence DR, Bacharach AL, editor. Pharmacometrics. Vol. 1. New York: Academic press New York; 1969. p. 161.  Back to cited text no. 11
    
12.Puri A, Saxena RP, Saxena KC, Srivastava V, Tandon JS. Immunostimulant activity of Nyctanthes arbortristis L. J Ethenopharmacol 1994;42:31-7.  Back to cited text no. 12
    
13.Khan T, Tatke P, Gabhe SY. Immunological studies on the aerial roots of the Indian Banyan. Indian J Pharm Sci 2008;70:287-91.  Back to cited text no. 13
[PUBMED]  Medknow Journal  
14.Raghuramulu N, Nair KM, Kalyanasundaram S. A Manual of Laboratory Techniques. Hyderabad, India: National Institute of Nutrition (NIN); 1983. p. 246-53.  Back to cited text no. 14
    
15.Bhattacharya. Manual Pre-conference, Annual conference of Indian Pharmacological society. Workshop on Research Methodology in pharmacology. 1993.  Back to cited text no. 15
    
16.Bhatt KR, Mehta RK, Srivastava PN. A simple method to assess anti-inflammatory activity. Ind J Physiol Pharmac 1977;21:399.  Back to cited text no. 16
    
17.Snedecor GW and Cochran WG. Statistical methods. 6 th ed. Ames, Iowa: Iowa State University Press; 1967. p. 258-96.   Back to cited text no. 17
    
18.Kondo M, Weissman IL, Akashi K. Identification of clonogenic common lymphoid progenitors in mouse bone marrow. Cell 1997;91:661-77.   Back to cited text no. 18
[PUBMED]  [FULLTEXT]  
19.Patwardhan B, Kalbag D, Patki PS, Nagasampagi BA. Search of Immunomodulatory Agents - a review. Indian Drugs 1991;28:249-54.  Back to cited text no. 19
    
20.Scanlon VC, Sanders T. Essentials of anatomy and physiology. 5 th ed. Philadelphia: F A Davis Company; 2003. p. 319-38.  Back to cited text no. 20
    
21.Vohra SB. Antibacterial, antipyretic, analgesic, and anti-inflammatory studies on Acorus calamus Linn. Ann Natl Acad Med Sci 1989;25:13-20.  Back to cited text no. 21
    
22.Dhir H, Agarwal K, Sharma A, and Talukder G. Modifying role of Phyllanthus emblica and ascorbic acid against nickel clastogenicity in mice. Cancer Lett 1991;59;9-18.  Back to cited text no. 22
    
23.Suresh K, Vasudevan DM. Augmentation of murine natural killer cell and antibody dependent cellular cytotoxicity activities by Phyllanthus emblica, a new immunomodulator. J Ethnopharmacology 1994;44:55-60.  Back to cited text no. 23
    
24.Tewari A, Sen SP, Guru LV. The effect of Amalaki (Phyllanthus emblica) Rasayana on biologic system. J Res Ind Med 1968;2:189.   Back to cited text no. 24
    
25.Sharma RC, Gupta SK, Khurana SC, Arora RB. Some Parmacological properties of Cyperus scariosus. Indian J Physiol Pharmacol 1970;14:38.  Back to cited text no. 25
    
26.Singh N, Kulshreshtha VK, Gupta HB, Bhargava KP. Pharmacological studies on Cyperus rotundus. Indian J Pharmacol 1969;1:19.  Back to cited text no. 26
  Medknow Journal  
27.Anonymus. Pharmacological Investigations of certain medicinal plants and compound formulations used in Ayurveda and Siddha. New Delhi: CCRAS; 1996. p. 282.  Back to cited text no. 27
    
28.Dahanukar SA, Karandikar SM, Desai M. Efficacy of Piper longum on childhood asthama. Indian Drugs 1984;21:384-8.  Back to cited text no. 28
    
29.Rege NN, Thatte UM, Dahanukar S. Adaptogenic properties of six Rasayana herbs used in Ayurvedic medicine. Phytotherapy Res 1999;13:275-91.  Back to cited text no. 29
    
30.Ali BH, Blunden G, Tanira MO, Nemmar MO. Some phytochemical, pharmacological and toxicological properties of ginger (zingiber officinale roscoe): A review of recent research. Food Chem Toxicol 2008;46:409-20.  Back to cited text no. 30
    
31.Sunila ES, Kuttan G. Immunomodulatory and anti-tumour activity of piper longum Linn. and Piperine. J Ethnopharmacol 2004;90:339-46.  Back to cited text no. 31
[PUBMED]  [FULLTEXT]  
32.Kassim M, Mansor M, Achoui M, Yan OS, Devi S, Yusoff KM. Honey as an immunomodulator during sepsis in animal model. Sepsis 2009;13:16.  Back to cited text no. 32
    
33.Marcucci MC. Propolis; chemical composition, biological properties and therapeutical utility. Apidologie 1995;26:83-9.  Back to cited text no. 33
    
34.Viuda Martos M, Ruiz-Navajas Y, Fern´Andez-L´Opez J, P´Erez-´Alvarez JA. Functional Properties of Honey, Propolis and Royal Jelly. J Food Sci 2008;73:116-24.  Back to cited text no. 34
    
35.Shriram Sheshgir Savrikar. 'Comparative Study of Physico-chemical characteristics of 'Accha Sneha' and 'Siddha Sneha' with reference to 'Guduchi Ghrita', the butter fat, medicated with Tinospora cordifolia (Willd.) Miers . PhD thesis submitted to Nanded, Maharashtra India: Swami Ramanand Teerth Marathwada University; 2006.  Back to cited text no. 35
    
36.Ashok BK. "A detailed investigation on the gender and formulation influences on the expression of pharmacological activity in Guduchi (Tinospora cordifolia (Willd.) Miers.)". PhD thesis submitted to Jamnagar, Gujarat, India: Gujarat Ayurved University; 2009.  Back to cited text no. 36
    



 
 
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