Login   |  Users Online: 36 Home Print this page Email this page Small font sizeDefault font sizeIncrease font size
Search Article 
  
Advanced search 
   Home | About us | Editorial board | Search | Ahead of print | Current issue | Archives | Submit article | Instructions | Subscribe | Contacts


 
  Table of Contents  
CLINICAL RESEARCH
Year : 2015  |  Volume : 36  |  Issue : 4  |  Page : 387-396  

Therapeutic evaluation of “Ayush Tulsi Jiwan Plus” oil for chronic musculoskeletal pain relief


1 Department of Pharmacology, IMS and SUM Hospital, SOA University, Bhubaneswar, Odisha, India
2 Department of Orthopaedics, IMS and SUM Hospital, SOA University, Bhubaneswar, Odisha, India
3 Central Research Institute of Ayurveda Drugs Development (Under CCRAS, New Delhi), Salt Lake, Kolkata, West Bengal, India
4 Department of Samhita Sharir, Institute of Post Graduate Ayurveda Medical Educations and Research, Shyamadas Vaidya Shastra Pith Hospital, Kolkata, West Bengal, India

Date of Web Publication16-Sep-2016

Correspondence Address:
Kunal Sharma
Resident and Tutor, Department of Pharmacology, IMS and SUM Hospital, P.O. Ghatikia, Bhubaneswar - 751 003, Odisha
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-8520.190687

Rights and Permissions
   Abstract 

Background: Chronic pain of musculoskeletal origin is a very common symptom and has major effect on the physical, mental, and economic aspects of the patients. There is always a crave among physicians and patients for effective analgesic, curable preparation that can be locally applied. Aim: The aim of this study is to assess the efficacy and safety of “Ayush Tulsi Jiwan Plus” oil in chronic pain management of musculoskeletal origin. Materials and Methods: Fifty patients of chronic musculoskeletal pain of unknown origin of mild to moderate condition were advised to apply “Ayush Tulsi Jiwan Plus” oil locally twice daily for 6 weeks and examined weekly. After completion of the treatment, the efficacy of the therapy was assessed on the basis of the subjective criteria such as perception of pain, tenderness, swelling, and joint mobility. Results: In this study, mean baseline score versus last visit score of pain (2.84 ± 0.68 vs. 1.33 ± 0.76), tenderness (1.64 ± 0.74 vs. 0.36 ± 0.56), and swelling (0.64 ± 0.85 vs. 0.38 ± 0.66) was significantly decreased, and also clinical improvement was seen in the study participants along with no evidence of adverse drug reactions. Conclusion: The analysis of the overall effect of this “Ayush Tulsi Jiwan Plus” oil preparation was found efficacious and topically safe in chronic pain conditions. However, further study will be required with larger sample size and in heterogeneous population to elicit long-term effect of this polyherbal preparation.

Keywords: Ayush Tulsi Jiwan Plus, chronic musculoskeletal pain, polyherbal oil


How to cite this article:
Sharma K, Sahoo J, Sahu D, Chattopadhyay A, Kumar S, Mishra SS. Therapeutic evaluation of “Ayush Tulsi Jiwan Plus” oil for chronic musculoskeletal pain relief. AYU 2015;36:387-96

How to cite this URL:
Sharma K, Sahoo J, Sahu D, Chattopadhyay A, Kumar S, Mishra SS. Therapeutic evaluation of “Ayush Tulsi Jiwan Plus” oil for chronic musculoskeletal pain relief. AYU [serial online] 2015 [cited 2017 May 29];36:387-96. Available from: http://www.ayujournal.org/text.asp?2015/36/4/387/190687


   Introduction Top


Chronic musculoskeletal pain is a common symptom of the human population. It has been reported since time immemorial. The most acceptable definition of chronic pain is the pain which last for more than 3–6 months.[1],[2] Another popular alternative definition of chronic pain, not required arbitrarily fixed timeline, is “pain that exerts beyond the expected period of healing.”[2] There is only a few cogent evidence for treating most types of chronic pain with opioids.[3]. Opioids may improve pain for the scrimpy duration but overall improvement in functioning and its analgesic effect is doubtful with high risk of overdose and dependence.[4] In the United States alone, about 100 million people have chronic pain, in which 25 million have more or frenetic chronic pain.[3]

Chronic pain may be further subdivided into “nociceptive” and “neuropathic” pain.[5] The superficial pain is originated by activation of nociceptors in the superficial tissues or skin, and the deep somatic pain is initiated by provocation of nociceptors in blood vessels, muscles, fasciae, ligaments, tendons, and bones. The temper of the deep somatic pain is poorly localized and dull-aching. Visceral pain is the pain originating from several visceral organs when inflamed or damaged due to any etiological factors.[6] Neuralgia (neuropathic pain) is divided into “peripheral neuropathic pain” and “central neuropathic pain” according to its origin.[7] The type of nerve fibers that are considered to propagate the chronic pain signals are C-fibers since these carry impulse in a very tardy nature and produce painful sensation that prevails for a long time.[8] Once the process is established, it is very difficult to reverse or eradicate in case of chronic pain.[9] In some genetic variants, the interference with neuronal differentiation leads to permanent reduction in the pain threshold, which ultimately results in chronic pain.[10]

Chronic musculoskeletal pain is mainly a consequence of a complex reciprocation of biochemical, mechanical, psychological, and social components.[11] Dynamic management of chronic pain is different from that of acute musculoskeletal pain to a great extent. Insight to the pain physiology, modulation, and perception is decisive for effective management. Pharmacotherapy and nonpharmacological therapies such as psychotherapy and biofeedback practice can be used to deal chronic pain. Many evidence-based therapeutic recommendations have been formed for chronic pain conditions such as low backache, osteoarthritic, neuropathic, and posttraumatic pain. However, complete and sustained subsidence of many types of chronic pain is difficult though some can be done to improve quality of life.[9] Apart from analgesics, limitations to conventional medical management of chronic pain indicate a genuine need for novel, safe, and effective treatments for these type of patients. Now, Ayurvedic medicine has been recognized by the World Health Organization as a complete system of natural medicine, which may have the potential to provide a solution to this problem.[12] In this study, the Ayurvedic polyherbal oil treatment for chronic musculoskeletal pain has been studied for its safety and efficacy and looked for the symptomatic relief without harmful side effects. Therefore, this study was in search for effective alternative and additional therapies for chronic pain.


   Materials and Methods Top


Outdoor patients, having chronic pain of musculoskeletal origin (e.g., low backache, knee, shoulder, elbow, wrist, ankle, and neck pain for more than 12 weeks) fulfilling the inclusion criteria, willingly ready to give informed written consent to participate in this study and also ready to attend scheduled outpatient department visits of Department of Orthopeadics, Institute of Medical Sciences and SUM Hospital, Bhubaneswar, Odisha, India, were screened for the present clinical trial. Total numbers of fifty patients were selected irrespective of sex, race, caste, religion, income, literacy, etc., However, some other data such as sociodemographic profile and relevant clinical data of participants were also recorded. The permission was taken from the Institutional Ethical Committee (No. 147-1/16/1/2015) and also registered to the Clinical Trial Registry of India (CTRI/2015/02/005523) before conducting this clinical trial.

Inclusion criteria

  • Patients of either sex aged between 25 and 65 years
  • Patients with idiopathic primary backache, knee pain, and any musculoskeletal pain for more than 12 weeks.


Exclusion criteria

  • History of any trauma/fractured joint/surgical/diagnostic intervention with reference to the affected joint(s)
  • Gross disability in performing daily normal routine, i.e., bed-ridden patients or confined to a wheelchair
  • Patients with co-morbidities such as gouty arthritis, rheumatoid arthritis, and psoriatic arthritis
  • Patients having any deformity of knee hip or back altering their gait and posture
  • Patients with uncontrolled hypertension (>160/100 mm of Hg)
  • Patients with uncontrolled diabetes mellitus (HbA1c >9%)
  • Patients with evidence of malignancy
  • Patients on prolonged (>6 weeks) medication with corticosteroids, antidepressants, anticholinergics, etc., or any other drugs that may have an influence on the outcome of the study
  • Patients who have a history of atrial fibrillation, acute coronary syndrome, myocardial infarction, stroke, or severe arrhythmia in the last 6 months
  • Patients with any severe renal or hepatic or any other disorder which may interfere in the study
  • Pregnant/lactating woman.
  • Patients who are currently participating in any other clinical trial
  • Any other condition which the Principal Investigator thinks may jeopardize the study.


Study design and drug intervention

This study was an open, prospective, and time bound clinical trial, performed in a small group of population with chronic pain to assess the efficacy and safety of the interventional drug “Ayush Tulsi Jiwan Plus” oil. The amount of “Ayush Tulsi Jiwan Plus” oil used was directly proportional to the area of the joint having pain. It was advised to apply locally as few drops for small joints and up to 2–3 ml for the larger joints, twice daily for 6 weeks. The formulation and percent composition of each ingredient of this oil has been decided and prepared by the sponsor [Table 1].
Table 1: Contents of “Ayush Tulsi Jiwan Plus” oil (polyherbal Ayurvedic formulation)

Click here to view


The patients were examined weekly, and suitable scoring pattern and objective signs were recorded to assess any change present in the patients. The initial findings were considered as baseline score, and subsequent scores at first visit (on 1st week), second visit (on 2nd week), third visit (on 3rd week), fourth visit (on 4th week), and last visit (on 6th week) were recorded. After completion of 6 weeks of the treatment, the efficacy of the therapy was assessed on the basis of the subjective criteria as stated below.

Perception of the pain

The slight modification was done in universally accepted, “The Faces Pain Scale” for easier assessment of pain and termed it as, “Modified Universal Pain Assessment Tool.”[13]



Swelling

In the similar way, the swelling and tenderness [14] assessment tools were applied for the proper and easier clinical assessment.



Tenderness



Joint mobility

The joint mobility was assessed in terms of severe restriction (about 75% loss of total joint mobility), moderate restriction (25–75% loss of total joint mobility), and mild restriction (<25% loss of total joint mobility).

Assessment of compliance

Among the various available methods to assess the compliance, integration method was used. On each visit, information regarding the use of oil was given to the every studied participant, and all participants were advised to bring their remaining oil container and empty bottles on the next visit. The participants were also interviewed regarding the use of the oil and residual volume of oil measurement done on every visit. The consumption of ≥80% of prescribed oil was considered as compliance.

Statistical analysis

The information gathered on the basis of above observations was subjected to statistical analysis. The data collected were analyzed using IBM SPSS Statistics for Windows. (Version 20.0. Armonk, NY: IBM Corp.). Continuous data were presented as mean values and standard deviation (SD) while categorical data were presented as percentages. Descriptive statistics were used to analyze the data, and results were represented in tabular form or graphically. The repeated measures ANOVA followed by Bonferroni post hoc analysis was used to evaluate the efficacy of the oil, taking consideration into baseline and last visit. The level of statistical significance (P value) was set at 0.05.

The subjective effect was decided on the basis of individual improvement in symptoms and the assessment tools parameters.

Observations

During the study period, a total of fifty patients were selected to participate in this study. All patients willingly provided consent and participated. Female patients (n = 27, 54.00%) participated more as compared to male patients (n = 23, 46.00%) [Figure 1]. The mean age of the study population was found to be 40.54 ± 11.31 years. Of 35 total study populations, overweight patients were 22 (44%) and obese patients were 13 (26%). Total 39 (78.00%) patients were under the age of 50 years, of which 20% patients were below 30 years [Figure 2]. The sociodemographic parameters of the study participants are shown in [Table 2].
Figure 1: Age and sex distribution of the chronic pain patients visited in outpatient department

Click here to view
Figure 2: Age distribution of the study participants

Click here to view
Table 2: Sociodemographic parameters of study participants

Click here to view


The clinical variables of all participants are shown in [Table 3]. The mean duration of pain was 8.16 ± 6.30 months and 64% of participants were suffering from knee pain and low backache. The patients having chronic pain of less than a year contributed more to this study (76%). The most common site of pain was low backache (34%), which was followed by knee pain (30%) in the study population. Thirty-two percent of the participants had multiple joint pain. Sixty percent of the participants presented with limitations of joint movement, in which only two patients with severe limitation of joint movement successfully qualified the screening criteria. The hypertensive and diabetic patients participated equally in this study (30% each). There were only two patients who had previous history of allergy: One with non-steroidal anti-inflammatory drug and another one with sulfur-containing drugs.
Table 3: Clinical variables of the study population

Click here to view



   Results Top


In this study, the appreciable differences seen between the mean scores of baseline and last visit of pain, tenderness, and swelling were 2.84 ± 0.68 versus 1.33 ± 0.76, 1.64 ± 0.74 versus 0.36 ± 0.56, and 0.64 ± 0.85 versus 0.38 ± 0.66, respectively. The pattern of mean score of pain, tenderness, and swelling gradually decreased on subsequent visits, which graphically represents downward slope [Figure 3],[Figure 4],[Figure 5].
Figure 3: Effect of “Ayush Tulsi Jiwan Plus” oil over pain

Click here to view
Figure 4: Effect of “Ayush Tulsi Jiwan Plus” oil over tenderness

Click here to view
Figure 5: Effect of “Ayush Tulsi Jiwan Plus” oil over swelling

Click here to view


The further statistical comparison of means was done by applying repeated measures ANOVA individually for pain, tenderness, and swelling and also found that there was a significant difference between the means on subsequent visits at P < 0.05 [Table 4]. Further Bonferroni post hoc test, was applied for visit-wise comparisons, which showed the significant difference in pain score in all the visits except in the second and 3rd third visit [Table 5]. There was also a significant difference in tenderness score, which was found in all visits except in 4th week visit and last (6th week) visit [Table 6]. The further significant difference in means of the swelling score was seen after third visit from the baseline [Table 7]. This oil has also shown the effect on joint mobility; 15 participants out of 17 showed excellent result over limitation to joint movement [Figure 6].
Table 4: Repeated measures ANOVA of “Ayush Tulsi Jiwan Plus” oil (Tests of Within-Subjects Effects)

Click here to view
Table 5: Bonferroni post hoc test (visit-wise comparisons over pain)

Click here to view
Table 6: Bonferroni post hoc test (visit-wise comparisons over tenderness)

Click here to view
Table 7: Bonferroni post hoc test (visit-wise comparisons over swelling)

Click here to view
Figure 6: Effect of “Ayush Tulsi Jiwan Plus” oil on joint movement

Click here to view


During the study period, no patient had any adverse reaction associated with this polyherbal oil preparation.


   Discussion Top


Chronic pain has a lot of impact on our day to day life. A review of recent literature observing the neurobiology and pathophysiology of chronic pain showed that this highly prevalent condition has negative impacts on multiple aspects of patient health such as sleep, cognitive processes and function of brain, mood or mental health, cardiovascular wellness, sexual function, and overall quality of life. In addition, the chronic pain can become more complex in its pathophysiology, and thus, it is potentially harder to treat over time. The chronic pain can also incur significant economic consequences along with various health complications for patients.[15]

The mean ± SD age of patients in this study was 40.54 ± 11.31 years with ranges between 25 and 65 years; this may be due to the strict inclusion and exclusion criteria and small number of study participants for this clinical trial. The female patients (54.00%) participated more as compared to males; this sex distribution is comparable to the study done in the elderly where females had more prevalence of chronic pain.[15] Seventy percent of total study participants were obese or overweight, which is in accordance to the previous study.[16],[17] A maximum number of patients, i.e. 78%, were under the age of 50 years, mainly due to other patients with chronic pain having other associated comorbidities or diagnosed with other autoimmune/inflammatory arthritic conditions were excluded from this study. Of fifty participants, 64% of participants were having chronic low backache and knee pain. The mean duration of pain in this study was 8.16 ± 6.30 months, which may be due to small sample size. The 16 participants had more than one joint pain, among these multiple joint pain patients, most of them had the history of pain more than a year which gradually increased by the time. The other common metabolic disorders such as, diabetes (30%) and hypertension (30%) were evenly distributed in this study group.

Mustard oil (Brassica juncea [L.] Czern.) contains about 60% monounsaturated fatty acids (42% erucic acid and 12% oleic acid), 21% polyunsaturated fatty acids (6% the omega-3 alpha-linolenic acid and 15% the omega-6 linoleic acid), and about 12% of saturated fats.[18] Omega-3 fatty acids have potency to improve rheumatoid arthritis due as its metabolites have inhibitory role in the production of inflammatory cytokines responsible for arthritic pain and also effective against arthritic pain as well as other symptoms, including joint stiffness.[19],[20] Mustard oil has stimulant and counter irritant properties and it is also mentioned in classical Ayurvedic literatures.[21] Due to these properties, it is included in “The Ayurvedic Pharmacopoeia of India”.[22]

Turpentine oil (Pinus bhutanica Grierson), has been used since ancient times. It is counter irritant, rubefacient, inflammation and swelling resolver. Turpentine oil may cause warmth and redness which can help relieve pain in the tissues underneath. It has been considered helpful for wound healing, treating scurvy, healing of ulcers, reducing vascular inflammation and valuable in the pain of rheumatic origin.[23],[24] Garlic (Allium sativum L.) has gained a reputation in various traditions as a prophylactic as well as therapeutic medicinal plant. It has played important dietary and medicinal roles throughout the history. Garlic has anti-inflammatory activity [25] and antibacterial property.[26],[27],[28]

Traditionally, almost all parts of Ratanjot (Onosma echioides L.) plants have medicinal properties.[29] Plants are used as a stimulant in bladder pain, palpitation of heart, kidney irritation, and rheumatism [30] while roots have cooling, astringent, demulcent, and diuretic action. O. echioides has various medicinal properties such as anti-inflammatory, antipyretic, analgesic, antiseptic, cardiac tonic, and wound healing. It is also used in skin disease.[31],[32],[33],[34],[35],[36]

Numerous studies on Pudina Satwa (Mentha longifolia [L.] Huds.) have shown various pharmacological and therapeutic effects of the plant.[37],[38]M. longifolia has significant antimicrobial activities,[39],[40] antinociceptive, antipyretic, antiemetic, antispasmodic, and carminative.[41],[42],[43] It has also central nervous system stimulant and antioxidant properties.[40]

Ajwain Satwa (Trachyspermum ammi Sprague.), with its characteristic aromatic smell and pungent taste, is widely used as a spice in curries. It has been shown to possess digestive stimulant,[44] hypolipidemic,[45] anti-inflammatory,[46] antimicrobial,[47] anthelmintic,[48] bronchodilating, antihypertensive, hepatoprotective, antispasmodic,[49] antilithiasis, diuretic,[50] abortifacient,[51] galactogogic,[52] antiplatelet-aggregatory,[53] antitussive,[54] antifilarial,[55] gastroprotective,[56] nematicidal,[57] anthelmintic,[48] detoxification of aflatoxins,[58] and ameliorative effects.[59]

Camphor (Camphora officinarum Baub.) has long been prescribed in traditional medicine for the treatment of inflammatory diseases such as musculoskeletal pains, rheumatic condition, sprains, and bronchitis. C. officinarum has anti-inflammatory mechanisms blocked the production of interleukin-1, interleukin-6, and tumor necrosis factor-α from RAW264.7 cells and nitrous oxide, prostaglandin E2 production in lipopolysaccharide or interferon-γ-activated macrophages.[60] Camphor has also diaphoretic action with mild analgesic properties.[61],[62]

In view of anti-inflammatory, antiseptic, and analgesic properties of each ingredient, hypothesis was made that this novel A yurvedic combination can have synergistic effect over chronic pain. Hence, clinical trial was conducted to observe the efficacy and safety of this polyherbal preparation.

In this study, mean baseline parameters versus last visit (i.e., 6th week) parameters of pain (2.84 ± 0.68 vs. 1.33 ± 0.76), tenderness (1.64 ± 0.74 vs. 0.36 ± 0.56), and swelling (0.64 ± 0.85 vs. 0.38 ± 0.66) were statistically decreased significantly, and also clinical improvement was seen in the study participants. The gradual downward slope of the means was observed due to gradual decrease in the mean score of pain, tenderness, and swelling, which suggests the efficacy of “Ayush Tulsi Jiwan Plus” oil, and decreasing trend of graphical representations of these parameters showed gradual improvements in subsequent follow-ups.

The effect of “Ayush Tulsi Jiwan Plus” polyherbal topical oil preparation has shown significance difference between its means in detailed statistical analysis. The means of pain score in all the visits were significantly decreased except in between the second and third visits. Significant difference in tenderness score was found in all visits except in 4th week visit and last (6th week) visit. The oil effect in swelling has been seen after 3 weeks of therapy as significant difference in means of the swelling score was seen only after third visit from the baseline. After application of this oil, a significant number of patients with decreased joint mobility were also improved. This may be due to the combined effect of decrease in pain, tenderness, and swelling, which contributed to improvement of joint condition and its mobility.

In the present study, only fifty patients (aged between 25 and 65 years) of chronic pain of unknown origin, those were in mild to moderate pain condition, were selected. Hence, further study will be required with larger sample size and in heterogeneous population. Regarding the efficacy of “Ayush Tulsi Jiwan Plus” oil, it was found effective for chronic pain of musculoskeletal origin and showed continuous reduction of pain, tenderness, and swelling and improvement of joint mobility with clinically significant results seen within 45 days of treatment. In view of zero evidence of major or minor adverse drug reaction, it is considered being safe as topical application.


   Conclusion Top


Concisely, this clinical study, which investigated the effects of “Ayush Tulsi Jiwan Plus” Oil on patients who were suffering from chronic pain of musculoskeletal origin, showed that this polyherbal topical preparation was effective in reducing patient's subjective pain, tenderness, and swelling along with improvement in joint mobility. These results suggest that the local application of “Ayush Tulsi Jiwan Plus” oil might be a valuable polyherbal preparation for chronic pain relief of musculoskeletal origin.

Acknowledgement

I acknowledge Dr. Soumya Santra, PG Resident, Dept. Of Pharmacology, IMS and SUM Hospital, for reviewing the manuscript.

Financial support and sponsorship

The trial was sponsored by the Ayush Arihant Industries Pvt. Ltd. Subash Chowk Rajgangpur, Sundergarh, Odisha.PIN 770017.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Debono DJ, Hoeksema LJ, Hobbs RD. Caring for patients with chronic pain: Pearls and pitfalls. J Am Osteopath Assoc 2013;113:620-7.  Back to cited text no. 1
    
2.
Turk DC, Okifuji A. Pain terms and taxonomies. In: Loeser D, Bustler SH, Chapman JJ, editors. Bonica's management of pain. 3. Philadelphia: Lippincott Williams and Wilkins; 2001. pp. 18–25.  Back to cited text no. 2
    
3.
Reuben DB, Alvanzo AA, Ashikaga T, Bogat GA, Callahan CM, Ruffing V, et al. National Institutes of Health Pathways to Prevention Workshop: The role of opioids in the treatment of chronic pain. Ann Intern Med 2015;162:295-300.  Back to cited text no. 3
    
4.
Franklin GM; American Academy of Neurol ogy. Opioids for chronic noncancer pain: A position paper of the American Academy of Neurology. Neurology 2014;83:1277-84.  Back to cited text no. 4
    
5.
Keay KA, Clement CI, Bandler R. The neuroanatomy of cardiac nociceptive pathways. In: Horst GJ, editor. The Nervous System and the Heart. Totowa, New Jersey: Humana Press; 2000. p. 304.  Back to cited text no. 5
    
6.
Coda BA, Bonica JJ. General considerations of acute pain. In: Loeser D, Bonica JJ, editors. Bonica's Management of Pain. 3rd ed. Philadelphia: Lippincott Williams & Wilkins; 2001.  Back to cited text no. 6
    
7.
Bogduk N, Merskey H. Classification of Chronic Pain: Descriptions of Chronic Pain Syndromes and Definitions of Pain Terms. 2nd ed. Seattle: IASP Press; 1994. p. 212.  Back to cited text no. 7
    
8.
Reddi D, Curran N, Stephens R. An introduction to pain pathways and mechanisms. Br J Hosp Med 2013;74:C188–91.  Back to cited text no. 8
    
9.
Vadivelu N, Sinatra R. Recent advances in elucidating pain mechanisms. Curr Opin Anaesthesiol 2005;18:540-7.  Back to cited text no. 9
    
10.
Rusanescu G, Mao J. Notch3 is necessary for neuronal differentiation and maturation in the adult spinal cord. J Cell Mol Med 2014;18:2103-16.  Back to cited text no. 10
    
11.
Uhl RL, Roberts TT, Papaliodis DN, Mulligan MT, Dubin AH. Management of chronic musculoskeletal pain. J Am Acad Orthop Surg 2014;22:101-10.  Back to cited text no. 11
    
12.
World Health Organization. Benchmarks for Training in Traditional/Complementary and Alternative Medicine: Benchmarks for Training in Ayurveda. Geneva, Switzerland: World Health Organization; 2010.  Back to cited text no. 12
    
13.
Hicks CL, von Baeyer CL, Spafford PA, van Korlaar I, Goodenough B. The faces pain scale-revised: Toward a common metric in pediatric pain measurement. Pain 2001;93:173-83.  Back to cited text no. 13
    
14.
Hubbard DR, Berkoff GM. Myofascial trigger points show spontaneous needle EMG activity. Spine (Phila Pa 1976) 1993;18:1803-7.  Back to cited text no. 14
    
15.
Fine PG. Long-term consequences of chronic pain: Mounting evidence for pain as a neurological disease and parallels with other chronic disease states. Pain Med 2011;12:996-1004.  Back to cited text no. 15
    
16.
McCarthy LH, Bigal ME, Katz M, Derby C, Lipton RB. Chronic pain and obesity in elderly people: Results from the Einstein aging study. J Am Geriatr Soc 2009;57:115-9.  Back to cited text no. 16
    
17.
Narouze S, Souzdalnitski D. Obesity and chronic pain: Systematic review of prevalence and implications for pain practice. Reg Anesth Pain Med 2015;40:91-111.  Back to cited text no. 17
    
18.
Entry for Mustard Oil in the United States Department of Agriculture, Agriculture Research Service. National Database for Standard Reference. Release 27. Available from: http://www.ndb.nal.usda.gov/ndb/foods/show/668?fg=&man=&lfacet=&count=&max=&sort=&qlookup=&offset=& format=Full&new=. [Last accessed on 2015 Apr 13].  Back to cited text no. 18
    
19.
Zainal Z, Longman AJ, Hurst S, Duggan K, Caterson B, Hughes CE, et al. Relative efficacies of omega-3 polyunsaturated fatty acids in reducing expression of key proteins in a model system for studying osteoarthritis. Osteoarthritis Cartilage 2009;17:896-905.  Back to cited text no. 19
    
20.
Goldberg RJ, Katz J. A meta-analysis of the analgesic effects of omega-3 polyunsaturated fatty acid supplementation for inflammatory joint pain. Pain 2007;129:210-23.  Back to cited text no. 20
    
21.
Panda H, Herbs cultivation and medicinal uses. Delhi: NIIR.2004, 183-4.  Back to cited text no. 21
    
22.
Anonymous. 1st ed. Vol. 6. New Delhi: Ministry of Health and Family welfare, Department of AYUSH Government of India; 2008. The Ayurvedic Pharmacopoeia of India, Part 1; 210.  Back to cited text no. 22
    
23.
Maroon JC, Bost JW, Maroon A. Natural anti-inflammatory agents for pain relief. Surg Neurol Int 2010;1:80.  Back to cited text no. 23
[PUBMED]  Medknow Journal  
24.
Seraj S, Jahan FI, Chowdhury AR, Monjur-Ekhuda M, Khan MS, Aporna SA, et al. Tribal formulations for treatment of pain: A study of the Bede community traditional medicinal practitioners of Porabari Village in Dhaka District, Bangladesh. Afr J Tradit Complement Altern Med 2012;10:26-34.  Back to cited text no. 24
    
25.
Sarrell EM, Cohen HA, Kahan E. Naturopathic treatment for ear pain in children. Pediatrics 2003;111(5 Pt 1):e574-9.  Back to cited text no. 25
    
26.
Janes ME, Nannapaneni R, Johnson MG. Identification and characterization of two bacteriocin-producing bacteria isolated from garlic and ginger root. J Food Prot 1999;62:899-904.  Back to cited text no. 26
    
27.
Bayan L, Koulivand PH, Gorji A. Garlic: A review of potential therapeutic effects. Avicenna J Phytomed 2014;4:1-14.  Back to cited text no. 27
    
28.
Viswanathan V, Phadatare AG, Mukne A. Antimycobacterial and Antibacterial Activity of Allium sativum Bulbs. Indian Journal of Pharmaceutical Sciences. 2014;76(3):256-261.  Back to cited text no. 28
    
29.
Kumar N, Kumar R, Kishore K. Onosma L.: A review of phytochemistry and ethnopharmacology. Pharmacogn Rev 2013;7:140-51.  Back to cited text no. 29
    
30.
Zhou L, Zheng G, Wang S, Gan F. Metabolic regulation of pigment formation of Onosma paniculatum cultured cells. Chin J Biotechnol 1992;8:263-8.  Back to cited text no. 30
    
31.
Kandemir A, Turkmen Z. The flora of Uzumlu-Sakaltutan (Erzincan-Gumuflhane). Turk J Bot 2008;32:265-304.  Back to cited text no. 31
    
32.
Teppner H. Remarks to the Onosma species O. bourgaei, O. spruneri and O. stellulata (Boraginaceae) offered. Samentauschverzeichnis. Bot. Garten Inst. Bot. Univ. Graz 1996;33-9.  Back to cited text no. 32
    
33.
Binzet R, Akcin OE. The anatomical properties of two Onosma L. (Boraginaceae) species from Turkey. J Med Plants Res 2012;6:3288-94.  Back to cited text no. 33
    
34.
Riedl H. Additional notes on Cwoiswa-species (Boraginaceae) from Turkey. Linzer Biol Beitr 1987;19:461-5.  Back to cited text no. 34
    
35.
Ghahremaninejad F, Joharchi M, Vitek E. New plant records for Khorassan province, Iran. Ann Narurhist Mus Wien B 2005;106:255-93.  Back to cited text no. 35
    
36.
Kandemir A, Hedge IC. An anomalous new Ferulago (Apiaceae) from Eastern Turkey. Willdenowia 2007;37:273-6.  Back to cited text no. 36
    
37.
Buckle J. Use of aromatherapy as a complementary treatment for chronic pain. Altern Ther Health Med 1999;5:42-51.  Back to cited text no. 37
    
38.
Mikaili P, Mojaverrostami S, Moloudizargari M, Aghajanshakeri S. Pharmacological and therapeutic effects of Mentha longifolia L. and its main constituent, menthol. Anc Sci Life 2013;33:131-8.  Back to cited text no. 38
    
39.
Mimica-Dukic N, Bozin B, Sokovic M, Mihajlovic B, Matavulj M. Antimicrobial and antioxidant activities of three Mentha species essential oils. Planta Med 2003;69:413-9.  Back to cited text no. 39
    
40.
Gulluce M, Sahin F, Sokmen M, Ozer H, Daferera D, Sokmen A, et al. Antimicrobial and antioxidant properties of the essential oils and methanol extract from Mentha longifolia L. ssp. longifolia. Food Chem 2007;103:1449-56.  Back to cited text no. 40
    
41.
Jan S, Khan MA, Uddin S, Murad W, Hussain M, Ghani A. Herbal recipes used for gastrointestinal disorders in Kaghan Valley, NWFP, Pakistan. Pak J Weed Sci Res 2008;14:169-200.  Back to cited text no. 41
    
42.
Khan SW, Khatoon S. Ethnobotanical studies on some useful herbs of Haramosh and Bugrote valleys in Gilbit, northern areas of Pakistan. Pak J Bot 2008;40:43-58.  Back to cited text no. 42
    
43.
Hussain K, Shahazad A, Zia-ul-Hussnain S. An ethnobotanical survey of important wild medicinal plants of Hattar District Haripur, Pakistan. Ethnobotanical Lealf 2008;12:29-35.  Back to cited text no. 43
    
44.
Vasudevan K, Vembar S, Veeraraghavan K, Haranath PS. Influence of intragastric perfusion of aqueous spice extracts on acid secretion in anesthetized albino rats. Indian J Gastroenterol 2000;19:53-6.  Back to cited text no. 44
    
45.
Kumari KS, Prameela M. Effect of incorporating Carum copticum seeds in a high fat diet for albino rats. Med Sci Res 1992;20:219-20.  Back to cited text no. 45
    
46.
Thangam C, Dhananjayan R. Antiinflammatory potential of the seeds of Carum copticum Linn. Indian J Pharmacol 2003;35:388-91.  Back to cited text no. 46
  Medknow Journal  
47.
Bonjar GH. Anti yeast activity of some plants used in traditional herbal-medicine of Iran. J Biol Sci 2004;4:212-5.  Back to cited text no. 47
    
48.
Priestley CM, Williamson EM, Wafford KA, Sattelle DB. Thymol, a constituent of thyme essential oil, is a positive allosteric modulator of human GABA(A) receptors and a homo-oligomeric GABA receptor from Drosophila melanogaster. Br J Pharmacol 2003;140:1363-72.  Back to cited text no. 48
    
49.
Gilani AH, Jabeen Q, Ghayur MN, Janbaz KH, Akhtar MS. Studies on the antihypertensive, antispasmodic, bronchodilator and hepatoprotective activities of the Carum copticum seed extract. J Ethnopharmacol 2005;98:127-35.  Back to cited text no. 49
    
50.
Ahsan SK, Shah AH, Tanira MO, Ahmad MS, Tariq M, Ageel AM. Studies on some herbal drugs used against kidney stones in Saudi folk medicine. Fitoterapia 1990;61:435-8.  Back to cited text no. 50
    
51.
Nath D, Sethi N, Srivastav S, Jain AK, Srivastava R. Survey on indigenous medicinal plants used for abortion in some districts of Uttar Pradesh. Fitoterapia 1997;68:223-5.  Back to cited text no. 51
    
52.
Kaur H. Estrogenic activity of some herbal galactogogue constituents. Indian J Anim Nutr 1998;15:232-4.  Back to cited text no. 52
    
53.
Srivastava KC. Extract of a spice – Omum (Trachyspermum ammi)-shows antiaggregatory effects and alters arachidonic acid metabolism in human platelets. Prostaglandins Leukot Essent Fatty Acids 1988;33:1-6.  Back to cited text no. 53
    
54.
Boskabady MH, Jandaghi P, Kiani S, Hasanzadeh L. Antitussive effect of Carum copticum in Guinea pigs. J Ethnopharmacol 2005;97:79-82.  Back to cited text no. 54
    
55.
Mathew N, Misra-Bhattacharya S, Perumal V, Muthuswamy K. Antifilarial lead molecules isolated from Trachyspermum ammi. Molecules 2008;13:2156-68.  Back to cited text no. 55
    
56.
Ramaswamy S, Sengottuvelu S, Haja SS, Jaikumar S, Saravanan R, Prasadkumar C, et al. Gastroprotective activity of ethanolic extract of Trachyspermum ammi fruit. Int J Pharm Biosci 2010;1:1-15.  Back to cited text no. 56
    
57.
Pelczar MJ, Chan EC, Krieg NR. Control of microorganism by physical agents. In: Microbiology. New York: McGraw Hill International; 1988. p. 469-509.  Back to cited text no. 57
    
58.
Velazhahan R, Vijayanandraj S, Vijayasamundeeswari A, Paranidharan V, Samiyappan R, Iwamoto T, et al. Detoxification of aflatoxins by seed extracts of the medicinal plant, Trachyspermum ammi (L.) Sprague ex Turrill structural analysis and biological toxicity of degradation product of aflatoxin G1. Food Control 2010;21:719-25.  Back to cited text no. 58
    
59.
Anilakumar KR, Saritha V, Khanum F, Bawa AS. Ameliorative effect of ajwain extract on hexachlorocyclohexane-induced lipid peroxidation in rat liver. Food Chem Toxicol 2009;47:279-82.  Back to cited text no. 59
    
60.
Lee HJ, Hyun EA, Yoon WJ, Kim BH, Rhee MH, Kang HK, et al. In vitro anti-inflammatory and anti-oxidative effects of Cinnamomum camphora extracts. J Ethnopharmacol 2006;103:208-16.  Back to cited text no. 60
    
61.
McGuffin M, Hobbs C, Upton R, Goldberg A. American Herbal Products Association's Botanical Safety Handbook. Boca Raton, FL: CRC Press, 1997. p. 153.  Back to cited text no. 61
    
62.
Sweetman SC. Martindale: The Complete Drug Reference. 36th ed. London: The Pharmaceutical Press; 2009. p. 2273.  Back to cited text no. 62
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
   Conclusion
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed1451    
    Printed13    
    Emailed0    
    PDF Downloaded224    
    Comments [Add]    

Recommend this journal