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Abstract

Psoriasis is a common inflammatory skin condition that can affect any region of the body and is characterised by red, scaly plaques. It mostly affects every body part, with the hands, feet, and limbs being most affected. In contrast to only 1-3% of contemporary medications, skin diseases are treated using almost one-third of all ancient treatments. While conventional treatments exist, many patients seek alternative natural therapies. This systematic review evaluates the efficacy and safety of dietary interventions, herbal remedies, mind-body therapies, and topical natural treatments for psoriasis. Herbal Remedies: Turmeric/Curcumin, Neem, Aloe vera, Tea tree oil, Mahonia aquifolium Mind-Body. Therapies: 1. Meditation/mindfulness 2. Yoga 3. Acupuncture 4. Hypnosis Topical Natural Treatments:1. Coconut oil 2. Olive oil3. Dead Sea salts4. Mud therapy5. Phototherapy (UVB, narrowband UVB)Herbal Remedies: 1. Turmeric/Curcumin2. Neem 3. Aloe vera4. Tea tree oil5. Mahonia aquifolium Mind-Body Therapies:1. Meditation/mindfulness 2. Yoga 3. Acupuncture 4.Hypnosis Topical Natural Treatments: 1. Coconut oil 2.Olive oil 3.Dead Sea salts 4.Mud therapy 5.Phototherapy (UVB, narrowband UVB) There are two categories for skin diseases: acute and chronic. Although there is usually no cure for chronic skin diseases, they can be controlled with medication. However, a great deal of medicinal plants are also utilized to cure skin condition.

Keywords

Psoriasis, Alternative medicine, Natural treatments, Dietary interventions, Herbal remedies, Mind-body therapies, Topical treatments.

Introduction

Psoriasis is a long-term, non-communicable, autoimmune inflammatory condition affecting the skin and joints. The Greek word Psora, which meaning itching, is where the name "psoriasis" originates.[1] The autoimmune disease psoriasis is a chronic, non-contagious condition marked by patches of defective skin. These areas are scaly, dry, itchy, and red, pink, or purple. Although there isn't a permanent cure for this chronic illness, there are some treatments that can be used to manage its symptoms. An autoimmune skin condition known as psoriasis, which affects 1-3% of people worldwide, is hyperproliferative Both men and women can get psoriasis, but women and those with a family history are more likely to develop it earlier in life. Most people believe that psoriasis is a hereditary condition brought on by environmental triggers. Although there isn't a recognized cure for psoriasis, there are treatments that can help manage the symptoms. Among these treatments are lotions containing steroids, vitamin D3, UV radiation, immunosuppressive medications like methotrexate and cyclosporins, and herbal remedies like aloe vera. Greek medical texts mention psoriasis as an illness, and patients with it were shunned by their communities. People's misunderstanding that psoriasis was an infectious disease was the primary cause of this. In addition to this misperception, psoriasis was not acknowledged by medical professionals in earlier times as a chronic, non-infectious dermatological condition.[2] Psoriasis is a chronic ailment that cannot spread to other parts of the body, yet it can affect skin. The severity of psoriasis can vary from quite mild to extremely significant. Psoriasis cannot currently be cured, although it can be effectively managed with a variety of treatments.[3] The incidence of the illness is 4.6% in developed nations worldwide.[4]

What organs are impacted by psoriasis?

On your skin, a psoriasis rash may appear anywhere.

Psoriasis frequently affects your:

Elbows

Lower back

Fingernails

Toenails

Face and inside your mouth

Chop

The hands and feet

Psoriasis causes include :

stress,

skin injuries

infections like strep throat

dry weather

heavy alcohol use

alterations in harmonic balance

smoking

skin injuries including cuts, scrapes, Insect bites

sunburns

Medications, including blood pressure medication

antimalarial medications

lithium and other mood stabilizer

antibiotic and NSAIDs

The signs of psoriasis

Individuals could encounter:

Joints: the source of pain

Skin: redness, fissures, rashes, and dryness

Additionally typical:

Depression

Itching

Minor  nail dents

Burning or painless

Psoriasis Complication :

Psoriasis can lead to several issues. When you receive the diagnosis, ask your physician:

Eye disorders such as pinkeye

Certain malignancies; psoriatic arthritis

Heart illness

Obesity

Psoriasis Types :

There are different kinds of psoriasis.

       
            Types Of Psoriasis.png
       

Fig.no 1: Types Of Psoriasis

1) Psoriasis plaque

Between 85% and 90% of people have plaque psoriasis, which is the most prevalent kind of the condition. It results in skin that is patchy and thick. Usually, they show up on the lower back, knees, elbows, etc. Usually, it has red areas with white scaling.

        
            Plaque Psoriasis.png
       

Fig.no 2: Plaque Psoriasis

Dermatitis guttate

Eruptive psoriasis, also known as guttate psoriasis, is frequently observed in children following an upper respiratory tract infection and streptococcal pathogen infection. It mostly affects the trunk and back, where it manifests as erythematous, scaly lesions shaped like raindrops

       
            Dermatitis guttate.png
       

Fig.no 3 : Dermatitis guttate

3)  Psoriasis in reverse

One skin disorder that affects the folds on your skin is called inverse psoriasis. In specific areas, you may notice red, glossy patches if you have inverse psoriasis. Skin folds beneath your breast, between your buttocks, and around your genital area, just like it does under your armpits. The skin may have cracks that are itchy, smell bad, or both. It may also be wet and macerated. Intertriginous psoriasis and flexural psoriasis are other names for inverse psoriasis.

       
            Inreverse Psoriasis.png
       

Fig.no 4 : Inreverse Psoriasis

Psoriasis pustular

One kind of psoriasis that results in pus-filled blisters on plaque is called pustular psoriasis. You may have pustular psoriasis on your hands and feet. There are two varieties: generalised and localised. Hypocalcaemia is linked to generalised pustular psoriasis, which manifests as sterile pustules on an erythematous plaque that covers the entire body.

       
            Pustular Psoriasis.png
       

Fig.no 5 : Pustular Psoriasis

Psoriasis erythrodermicum

A rare skin disorder called erythrodermic psoriasis results in a crimson rash that covers much of your body. Erythrodermic psoriasis, the least prevalent kind of psoriasis, can cause a peeling rash that might burn or itch all over the body. Psoriasis can be either acute or persistent. When erythrodermic psoriasis occurs, more than 90% of the body is covered in exfoliated skin and erythema, a widespread kind of inflammation. Severe discomfort, swelling, and itching are linked to it.

       
            Erythrodermicum Psoriasis.png
       

Fig.no 6 : Erythrodermicum Psoriasis

6) Nail psoriasis

Psoriasis can affects your nails,too. When it does it’s called nail psoriasis. Nail psoriasis also known as psoriatic nail dystrophy. Fingernails and toenails can be affected by nail psoriasis. It causing abnormal nail growth and discoloration. Nail changes in psoriasis are seen as pitting, oil spots, subungual

hyperkeratosis, nail dystrophy, and anchylosis. If you have Psoriasis, it’s important to check your Fingernails and toenails for signs of nail psoriasis.

 Common signs includes:

• Tiny dents in your nails

• White, yellow, or brown discoloration

• Crumbling nails

• Nail (s) separating from your finger

• Build up beneath your nail

• Blood under your nail

       
            Nail Psoriasis.png
       

Fig.no 7 : Nail Psoriasis

Pathophysiology:

The study of the pathophysiology of psoriasis has significantly advanced our understanding of skin biology in general. Over the last fifteen years, advances in our knowledge of the pathophysiology of psoriasis have resulted in very successful, targeted therapies that have given us a better understanding of the pathophysiology of chronic inflammatory illnesses that are dominated by the IL-23/Th17 axis

       
            Pathophysiology of Psoriasis.png
       

Fig no. 8 :  Pathophysiology of Psoriasis

Dendritic cells are recognized to be important during the early phases of illness. Professional antigen- presenting cells are dendritic cells. It's unclear exactly how they are activated in psoriasis, though. The identification of antimicrobial peptides (AMPs), which are overexpressed in psoriatic skin and released by keratinocytes in reaction to damage, is one of the hypothesized processes. The most researched AMPs linked to psoriasis include S100 proteins, ?-defensins, and LL37. It has been suggested that LL37 or cathelicidin plays a pathogenic function in psoriasis. injured keratinocytes release it, and it then combines with self-genetic material from other injured cells to form complexes. Toll-like receptor (TLR) 9 in plasmacytoid dendritic cells (pDCs) is stimulated by LL37 coupled to DNA.

The production of type I IFN (IFN-? and IFN-?) is a hallmark of pDC activation, which is crucial in

initiating the development of psoriatic plaque. Myeloid dendritic cells (mDC) phenotypic maturation is facilitated by type I IFN signaling, which has also been linked to Th1 and Th17 differentiation and function, including the generation of interleukin (IL)-17 and IFN-?, respectively. LL37 coupled to RNA activates pDCs through TLR7, whereas LL37–DNA complexes stimulate pDCs through TLR9. Furthermore, mDCs are impacted by LL37–RNA complexes through TLR8. Tumor necrosis factor (TNF)-?, IL-23, and IL-12 are secreted by activated mDCs when they migrate into draining lymph nodes; the latter two factors influence the differentiation and proliferation of Th1 and Th17 cell subsets, respectively. Additionally, LL37-RNA activation causes slan+ monocytes—important pro-inflammatory cells present in psoriasis skin lesions—to secrete large amounts of TNF-?, IL-12, and IL-23. The maintenance phase of psoriatic inflammation is driven by the activation of the adaptive immune response through the various T cell subsets. In the epidermis, Th17 cytokines, specifically IL-17, IL-21, and IL-22, stimulate keratinocyte growth. Through TNF-?, IL-17, and IFN-?, the inflammatory environment stimulates keratinocyte growth. Additionally, LL37 and DNA stimulate keratinocytes, which significantly boost type I IFN synthesis. Additionally, they actively contribute to the inflammatory cascade by secreting AMP, chemokines, and cytokines (IL-1, IL-6, and TNF-?). The TLR7/8 disease initiation concept is supported by a commonly used psoriasis-like inflammatory animal model that depends on the action of the TLR7/8 agonist imiquimod. Furthermore, mice lacking IL-23 or IL-17R could not respond to imiquimod, indicating that the IL-23/IL-17 axis plays a role in skin inflammation and psoriasis-like pathogenesis. Psoriasis of the plaque type is characterized by the TNF?– IL-23–Th17 inflammatory cascade. There are six members of the IL-17 cytokine family: IL-17A–F. They are crucial modulators of inflammatory responses and are generated by various cell types. As of right now, IL-17A and IL-17F are primarily responsible for the clinically significant signaling in psoriasis; they both operate via the same receptor but have varying potencies. The effects of IL-17A and IL-17F heterodimers are moderate, with IL-17A having a greater effect than IL-17F. The ACT1 adaptor protein is drawn in when IL-17A attaches to its trimeric receptor complex, which is made up of two IL- 17RA subunits and one IL-17RC subunit. A number of intracellular kinases, such as extracellular signal- regulated kinase (ERK), p38 MAPK, TGF-beta-activated Kinase 1 (TAK1), I-kappa B kinase (IKK), and glycogen synthase kinase 3 beta (GSK-3 beta), are activated when ACT1 and the IL-17 receptor complex interact.

The transcription of pro-inflammatory cytokines, chemokines, and antimicrobial peptides is made possible by these kinases through NF?B, AP-1, and C/EBP. While Th17 responses are driven by ACT1 and NF?B, Th1 and Th2 cytokines function via Janus kinase (JAK)-STAT signaling pathways . On the other hand, ?? T cells can generate IL-17A without the IL-23 stimulation . Plaque psoriasis can be effectively managed clinically with medications that target TNF?, IL-23, and IL-17 as well as signaling pathways like JAK/STAT.[5]

Psoriasis and Stress :

Stress and psoriasis have intricate relationships. A review of the research on the connection between stress and psoriasis is suggested in this article. Patients say that stress is a trigger for their psoriasis in 31– 88% of cases. Additionally, those who experienced a stressful incident in the last year reported a higher incidence of psoriasis, indicating that stress may have a role in causing the illness among predisposed individuals. Psoriasis breakouts can also lead to stress. When suggesting treatment to psoriasis sufferers, it is appropriate to address stress because of its function. People with psoriasis have shown success with behavioral and cognitive stress management therapy, biofeedback, hypnosis, and relaxation in a number of controlled studies.[6]

Climatotherapy :

The use of climate therapy Alternative therapeutic approaches known as "climatotherapy" make use of the restorative properties of natural elements such as light, temperature, humidity, air, and barometric pressure.One For thousands of years, people have utilized sea and spa water and items for their therapeutic and restorative qualities. Hippocrates even proposed that an imbalance in bodily fluids is the root cause of all illnesses. He suggested changing routines and surroundings, such as taking a bath, sweating, walking, and getting a massage, in order to achieve equilibrium. Seawater was one of the most popular medicinal substances in the history of the Mediterranean people during the Greek and Roman eras. A well-known quote from one of Euripides' tragedies is "sea water cures all human diseases." 2. Galen (131–201 CE), who lived during the Roman era, also promoted the use of water to heal a number of illnesses.[7]

Another Natural Treatment For Psoriasis :

Herbal remedies do not cause as many adverse effects as synthetic medications do. Herbal remedies are becoming increasingly essential in the treatment of inflammatory diseases of the skin. Herbal remedies are widely accessible. A change in food and lifestyle may help alleviate the symptoms of psoriasis, according to certain research. A few herbal remedies for treating psoriasis naturally and the potential explanation for thair's anti-psoriatic effects.

Aloe vera

Family - Liliaceae

Common name: Kathalai

aloes plant parts: leaf

Aloe Vera is a well-known plant that is used to treat thermal damage and cosmetic concerns. The green to grey-green leaves are meaty and thick. In theory, aloe vera gel may aid in reducing inflammation, which causes psoriasis symptoms on the skin and joints. Salicylic acid, steroids, antraquinones, and saponins are found in aloe vera and have antibacterial properties. The active ingredients have strong anti-inflammatory, analgesic, and wound-healing properties. Its anti- inflammatory characteristics, supporting the idea that aloe vera is a useful treatment for psoriasis.[8,9]

Angelica sinensis

Family: Apiaceae 

Common Name : Chinese

angelica Utilised plant parts: root

People refer to it dung quay. Angelicas are members of the Apiaceae family and are either biennials or short-lived perennials. When oral treatment with these plant extracts was administered to psoriasis patients, two thirds of the patients experienced total alleviation from their condition (Koo & Arain, 1998).[10,11,12]

Azadirachta  indica

Family : Meliaceae

Common name: Veppam, neem

Used plant parts : stem, bark, and leaves.

Burning the stem bark leaves ash that is applied topically on boils. A leaf decoction bath is used to cure Infections on the body. The same condition is also treated by taking its decoction orally. The oil from the seeds is used to cure dandruff and eradicate lice.[13]The bark and leaves possess antiviral and antibacterial qualities.

Zingiberaceae, or Alpinia galanga

Family: zingiberaceae

Common name: Akkulati, Thai

Ginger Plant parts used : Rhizome

The leaves of Thai ginger grow up to around five feet in height. Galanga has long been used in traditional medicine to treat a variety of conditions, such as psoriasis, inflammation, and microbial infections. It also functions as an anti-inflammatory and anti-cancer agent. The anti- psoriatic properties of the plants Annona squamosa, curcuma longa, and Alpinia galanga were reported by Chanachai et al. (2009).[14]  

Curcuma Longa

Family: Zingiberaceae Common name

Termeric Used plant parts: rhizome

As a rhizomatous herb, tarragon can reach a height of three to five feet.  The section of the rhizome that the herb that has therapeutic uses. Additionally, it has been found that decreased phk activity in groups treated with curcumin and calciumpotriol correlated with decreased keratinocyte transferrin receptor expression, as well as decreased densities of epidermal CD8+T cells and parakeratosis severity.[15]

Matricaria recutita

Family: Asteraceae

Common name: mookuthi poo, chamomile Plant parts used: Flower

M. chamomilla had long, narrow leaves and an upright, smooth, branching stem. There is evidence to suggest that psoriasis plaques are associated with elevated LTB4 development. [16,17]

Mahonia aquifolium

Family: Berberidaceace

Common name: oregon grape

Plant parts used – stem and leaves

Mahonia aquifolium is a flowering plant that comes from the mahonia shrub. It is very popular plant used in skin disorders, especially in psoriatic plaques. It is also called as barberry or oregon grape. The stem and leaves of the plant can be ground into a powder or distilled into an extract that is then used to manufacture a topical skin lotion. Mahonia aquifolium includes berberine, which may help to decrease some of the inflammation that psoriasis generates. Additionally, the herb exhibited antiproliferative properties, which means that it can inhibit skin cell proliferation.

Nigella sativa

Family: Ranunculaceae

Common name: Karunjiragam, Black

Cumin Used portion of plant: seeds

The seeds are administered externally to promote skin eruption. The seeds are traditionally used to treat psoriasis tropicalus, which causes patches to appear and generalised pain.[18]

Pharmacological studies on the seed extract show that it has a variety of properties, including as anti-inflammatory, antibacterial, antifungal, and anthelminthic properties.[19]

Simplex Phyllanthus

family: Phyllanthaceae

Common name: leaf behind the seed

used the entire plant as a plant component

The seed beneath the leaf is a hairless, slender plant that grows to a height of 60 cm and is woody in the lower portion. Tiny blossoms dangle on thin stalks.[20]

Marianum Silibum

Family: Asteraceae

Common name: Vishnu kranti, or milk thistle

Studies on milk thistle have demonstrated its ability to prevent psoriasis-related human T-cell activation.[21] Most people refer to it as milk thistle. It is generally known that this plant has hepatoprotective properties.

Smilax china

Family - smilacaceae

Common name: Parangichekkai, or China root

plant portion used: rhizome

China Smilax Linn. Used to treat a variety of illnesses, including psoriasis, rheumatism, gout, epilepsy, skin conditions, long-term neurological disorders, syphilis, flatulence, dyspepsia, constipation, colic, neuralgia, and seminal weakness.[22,23]

Thespesia populnea

Family : Malvaceae

Common name: Puvarasu, Indian tulip tree

Plant part used: Bark

It has long been believed that the Indian tulip tree, Thespesia populnea, can help with skin conditions like psoriasis, ringworm, dermatitis, and herpes infection. External application of coconut oil-boiled powdered bark is used to treat psoriasis.[24]

Ulmus rubhra Family: Ulmacea

Common name: Slipperyelm

Plant parts used: Barks

It is sometimes referred to as slippery elm, so called because of the mucilage component that comes from the elm's inner bark. Native Americans applied this extract topically on wounds, boils, and plaque-type psoriasis.[25]

Indica Urgenia

Family : Liliaceae

Common name: I Narivengayam, Indian squil Used plant portion: bulbs

has been applied to psoriasis treatment.[26]

Tinctoria Wrightia L. Family: Apocynaceae

Common name: Paalai, delicious Indrajao

When compared to isoretinoic acid as the reference, the hydroalcoholic extract of Wrightia tinctoria leaves was found to have a substantial anti-psoriatic impact in the mice tell test model. Significant orthokeratotic response, strong antioxidant activity in DPPH, nitric oxide, and hydrogen peroxide scavenging assays were seen in the extract.[27,28]

Biosimilars in psoriasis :

The current pharmaceutical arsenal is being revolutionized by the emergence of biosimilars for various diseases. Biosimilar versions of numerous biologics are being developed or are currently on the market as their patents are about to expire. A biosimilar is a biological product that satisfies two criteria: it must be very similar to an approved biologic product and, when compared to the reference product, it must not differ clinically in any significant ways in terms of safety, purity, or potency. The World Health Organization, the FDA, and the European Medicines Agency have all released guidelines for the creation and approval of biosimilars. Currently, Europe has approved two etanercept biosimilars, four infliximab biosimilars, and eight adalimumab biosimilars. Biosimilars have the potential to expand access to biologics by reducing the cost of systemic treatment for psoriasis patients.[29]

Final Verdict (Conclusion)

In the dermatological world, psoriasis is still a common condition, but for a variety of reasons, it is still seen as an underdiagnosed and improperly treated condition. The synthetic medications used to treat it have side effects, and some of them have been observed to cause psoriasis. Then the obvious choice—a herbal natural medicine that is both safe and just as effective as synthetic medications—is the herbal remedy. The majority of contemporary medications originate from plants, either directly or indirectly. This article has emphasised many plant sources based on reports from various studies and traditional knowledge. The publication also mentions the investigative factors, which are the key components for screening for herbal medications. This information should be helpful to researchers studying this topic.

REFERENCES

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  2. Boehncke, W. H., & Schön, M. P. Diseaseburden and epidemiology. Lancet. 2015;386,983-994.
  3. https://www.sign.ac.uk/pdf/pat121.pdf
  4. Parisi R, Symmons DPM, Griffiths CEM,Ashcroft DM. The Identification and Management of Psoriasis and Associated Comorbidity project Team. Globalepidemiology of psoriasis: a Systematic review of incidence and prevalence. J In
  5. Adriana Rendon Knut Schakel https://pubmed.ncbi.nlm.nih.gov/?term=Rendon+A&c
  6. Laurie Rousset MD Bruno Halioua MD https://onlinelibrary.wiley.com/authored-by/Rousset/Laurie
  7. Jana Kazandjieva MD, Ivan Grozdev MD, Razvigor Darlenski MD, Nikolai Tsankov MD Department of Dermatology and Venereology, Medical Faculty, Sofia, Bulgaria, 1431 Sofia, Bulgaria
  8. Dhanabal SP, Priyanka Dwarampudi L,Muruganantham N, Vadivelan R. (2012)Evaluation of the antipsoriatic Activity of Aloe vera leaf extract using a mouse tail Model of psoriasis. Phytother Res. 26:617–19.
  9. Klein AD, Penneys NS. Aloe vera. (1988)J Am Acad Dermatol. 18:714-720.
  10. Thitiporn Charueksereesakul visa Thongrakard and Tewin Tencomnao, (2011)In Vitro Effect of Thai herbal Extracts with anti-psoriatic activity on the expression of Caspase 9J. Chem. Pharm. Res. 3(4):196-203.
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  12. Koo J, Arain S. (1998) Traditional Chinese medicine for The treatment of dermatologic disorders. Arch Dermatol. 134: 1388- 1393.
  13. Mundada et al. A. S. Mundada, m.s. Mahajan,h.h. Gangurde, v.s. Borkar, v. S. Gulecha, r.a. Khandare (2009)formulation and evaluation of polyherbal Antipsoriatic cream pharmacology online 2: 1185-1191
  14. Saelee C, Thongrakard V, Pencomnao T. (2011) Effects Of high medicinal herb extract with anti-psoriatic Activity on the expression of NF-KB signaling Biomarkers in HaCaT keratinocytes. Molecules.16:3908-32
  15. Joe B, Lokesh BR. (1997) Effect of curcumin and Capsaicin on arachidonic acid metabolism and Lysosomal enzyme secretion by rat peritoneal Macrophages. Lipids, 32:1173-1180.
  16. Murti K, Panchal MA, Gajera V, Solanki J. (2012) Pharmacological properties of Matricaria recutita: A Review. Pharmacologia, 3:348-51.
  17. H, Sabieraj J, Sailer ER, Ammon HP. Chamazulene: (1994) an antioxidant-type inhibitor of Leukotriene B4 formation. Planta Medica, 60:410-413.
  18. Dwarampudi LP, Palaniswamy D, Nithyanantham M,Raghu PS. (2012) Anti-psoriatic activity and cytotoxicity Of ethanolic extract of Nigella sativa seed. Pharmacogn Mag. 8:268-72. 120
  19. Ghosheh OA, Houdi AA, Crooks PA. (1999) High Performance liquid chromatographic analysis of the Pharmacologically active quinones and related Compounds in the oil of the black seed (Nigella sativa L.) J Pharm Biomed Anal. 19:757–62.
  20. Sushil K. Chouhan HS, Sahu AN, Narayan G.Singh (2015)Assessment of in vitro antipsoriatic activity of Selected Indian medicinal plants Pharmaceutical Biology Volume 53, Issue 9, pages 1295-1301.
  21. Sabir S, Arsshad M, Asif S, Chaudhari SK. (2014) An Insight into medicinal and therapeutic potential of Silybum marianum (L.) Gaertn. Int J Biosci. 4:104-15.
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  30. RGB Langley, G G Krueger, CEM Griffiths

Reference

  1. Ritchlin, Christopher; Fitzgerald, Oliver.Psoriatic and Reactive Arthritis: A Companion to Rheumatology (1st ed.). Maryland Heights,Miss: Mosby; 2007. P.4. ISBN 978-0-323-03622.
  2. Boehncke, W. H., & Schön, M. P. Diseaseburden and epidemiology. Lancet. 2015;386,983-994.
  3. https://www.sign.ac.uk/pdf/pat121.pdf
  4. Parisi R, Symmons DPM, Griffiths CEM,Ashcroft DM. The Identification and Management of Psoriasis and Associated Comorbidity project Team. Globalepidemiology of psoriasis: a Systematic review of incidence and prevalence. J In
  5. Adriana Rendon Knut Schakel https://pubmed.ncbi.nlm.nih.gov/?term=Rendon+A&c
  6. Laurie Rousset MD Bruno Halioua MD https://onlinelibrary.wiley.com/authored-by/Rousset/Laurie
  7. Jana Kazandjieva MD, Ivan Grozdev MD, Razvigor Darlenski MD, Nikolai Tsankov MD Department of Dermatology and Venereology, Medical Faculty, Sofia, Bulgaria, 1431 Sofia, Bulgaria
  8. Dhanabal SP, Priyanka Dwarampudi L,Muruganantham N, Vadivelan R. (2012)Evaluation of the antipsoriatic Activity of Aloe vera leaf extract using a mouse tail Model of psoriasis. Phytother Res. 26:617–19.
  9. Klein AD, Penneys NS. Aloe vera. (1988)J Am Acad Dermatol. 18:714-720.
  10. Thitiporn Charueksereesakul visa Thongrakard and Tewin Tencomnao, (2011)In Vitro Effect of Thai herbal Extracts with anti-psoriatic activity on the expression of Caspase 9J. Chem. Pharm. Res. 3(4):196-203.
  11. Bhuchar S, Katta R, Wolf J. (2012) Complementary and Alternative medicine in dermatology: An overview of Selected modalities for the practicing dermatologist. Am J Clin Dermatol. 13:311-317.
  12. Koo J, Arain S. (1998) Traditional Chinese medicine for The treatment of dermatologic disorders. Arch Dermatol. 134: 1388- 1393.
  13. Mundada et al. A. S. Mundada, m.s. Mahajan,h.h. Gangurde, v.s. Borkar, v. S. Gulecha, r.a. Khandare (2009)formulation and evaluation of polyherbal Antipsoriatic cream pharmacology online 2: 1185-1191
  14. Saelee C, Thongrakard V, Pencomnao T. (2011) Effects Of high medicinal herb extract with anti-psoriatic Activity on the expression of NF-KB signaling Biomarkers in HaCaT keratinocytes. Molecules.16:3908-32
  15. Joe B, Lokesh BR. (1997) Effect of curcumin and Capsaicin on arachidonic acid metabolism and Lysosomal enzyme secretion by rat peritoneal Macrophages. Lipids, 32:1173-1180.
  16. Murti K, Panchal MA, Gajera V, Solanki J. (2012) Pharmacological properties of Matricaria recutita: A Review. Pharmacologia, 3:348-51.
  17. H, Sabieraj J, Sailer ER, Ammon HP. Chamazulene: (1994) an antioxidant-type inhibitor of Leukotriene B4 formation. Planta Medica, 60:410-413.
  18. Dwarampudi LP, Palaniswamy D, Nithyanantham M,Raghu PS. (2012) Anti-psoriatic activity and cytotoxicity Of ethanolic extract of Nigella sativa seed. Pharmacogn Mag. 8:268-72. 120
  19. Ghosheh OA, Houdi AA, Crooks PA. (1999) High Performance liquid chromatographic analysis of the Pharmacologically active quinones and related Compounds in the oil of the black seed (Nigella sativa L.) J Pharm Biomed Anal. 19:757–62.
  20. Sushil K. Chouhan HS, Sahu AN, Narayan G.Singh (2015)Assessment of in vitro antipsoriatic activity of Selected Indian medicinal plants Pharmaceutical Biology Volume 53, Issue 9, pages 1295-1301.
  21. Sabir S, Arsshad M, Asif S, Chaudhari SK. (2014) An Insight into medicinal and therapeutic potential of Silybum marianum (L.) Gaertn. Int J Biosci. 4:104-15.
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Mayuri Raut
Corresponding author

Nandkumar Shinde College of Pharmacy Vaijapur, Maharashtra: 423701

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Shivprasad Deokar
Co-author

Nandkumar Shinde College of Pharmacy Vaijapur, Maharashtra: 423701

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Dr. Kawade Rajendra M.
Co-author

Nandkumar Shinde College of Pharmacy Vaijapur, Maharashtra: 423701

Mayuri Raut*, Sivprasad Deokar, Dr. Kawade Rajendra M., Alternative Natural Treatment of Psoriasis, Int. J. of Pharm. Sci., 2024, Vol 2, Issue 12, 553-562. https://doi.org/10.5281/zenodo.14282435

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