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Cissampelos sympodialis Eichl (Menispermaceae) leaf extract as a possible novel and safe treatment for psoriasis

LETTER TO THE EDITOR

Cissampelos sympodialis Eichl (Menispermaceae) leaf extract as a possible novel and safe treatment for psoriasis

Amir FeilyI; Mohammad Reza NamaziII

IMD. Resident in Dermatology, Department of Dermatology, Jondishapur University of Medical Sciences, Ahvaz, Iran

IIMD. Assistant professor in the Dermatology, Medicinal and Natural Product Chemistry Research Center and Dermatology Department, Shiraz University of Medical Sciences, Shiraz, Iran

Address for correspondence Address for correspondence: Amir Feily Jondishapur University of Medical Sciences Ahvaz, Iran Tel: 00989177204638 E-mail: Dr.feily@yahoo.com E-mail: namazi_mr@yahoo.com

Psoriasis is an inflammatory disorder characterized by a T helper cell type 1 cytokine pattern. Interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), interleukin-2 (IL-2) and interleukin-1 (IL-1) are predominantly expressed in this disorder. This immunological pathway is stimulated by interleukin-12 (IL-12) released from activated dendritic cells and by exposure of T cells to type 1 cytokines during maturation.1 Systemic administration of T helper 2 (Th2) cytokines such as interleukin-4 (IL-4) or interleukin-10 (IL-10) neutralizes the T helper 1 (Th1) bias and improves psoriasis.2,3 TNF-α is believed to be a key pro-inflammatory cytokine involved in psoriasis pathogenesis, and anti-TNF blockers initially developed for rheumatoid arthritis therapy have dramatically decreased the clinical activity of psoriasis lesions.4 In psoriatic epidermis, the level of cyclic adenosine monophosphate (cAMP) decreases. It has been reported that beta-blockers may exacerbate psoriatic plaques through decreasing the concentration of intracellular cAMP. Topical caffeine, which is a methylxanthine, induces a higher concentration of intracellular cAMP and hence is an effective treatment for psoriasis.5 Nitric oxide synthesis is increased in psoriasis and a role for nitric oxide in the development of psoriasis has been suggested by some researchers.1

Leaves from Cissampelos sympodialisEichl (Menispermaceae) were collected in João Pessoa, State of Paraíba, Brazil, in January 1998. Infusions of C. sympodialis roots are popularly used in northeastern Brazil for treating asthma, bronchitis and rheumatism, among other inflammatory diseases. The immunomodulatory effect of the aqueous fraction of the ethanolic extract of the leaves (AFL) of C. sympodialis has been described. This effect was associated with inhibition of IL-2 production and increased production of both IL-10 and IL-4. AFL thus has a potent anti-inflammatory effect through downregulation of inflammatory cytokines.6

It has been shown that AFL inhibits cyclic nucleotide phosphodiesterase activity and increases cAMP levels in intact smooth cell cultures, pig bronchoalveolar leukocytes and murine B cells. Recent findings have shown that cAMP mimetic or activating reagents inhibit secretion of both TNF-alpha and IL-12 by activated peritoneal macrophages. This inhibitory effect has been shown to be mediated by increased IL-10 secretion. It has also been shown that AFL increased Trypanosoma cruzi growth through reduction of NO production. This effect may be mediated by an autocrine mechanism that depends on secretion of IL-10 by macrophages.6

Taking all the above facts together, given the potent effect of AFL towards decreasing the production of NO and inflammatory cytokines involved in the pathogenesis of psoriasis and increasing the production of anti-inflammatory cytokines (which are known to ameliorate this disease), we hereby suggest that Cissampelos sympodialis Eichl (Menispermaceae) leaf extract could be a novel and safe addition to the antipsoriatic weaponry.

Sources of funding: Not declared

Conflict of interest: Not declared

Date of first submission: January 19, 2009

Last received: February 16, 2009

Accepted: March 17, 2009

  • 1. Namazi MR. Nicotinamide: a potential addition to the anti-psoriatic weaponry. FASEB J. 2003;17(11):1377-9.
  • 2. Kimball AB, Kawamura T, Tejura K, et al. Clinical and immunologic assessment of patients with psoriasis in a randomized, double-blind placebo-controlled trial using recombinant human interleukin 10. Arch Dermatol. 2002;138(10):1341-6.
  • 3. Ghoreschi K, Thomas P, Breit S, et al. Interleukin-4 therapy of psoriasis induces Th2 responses and improves human autoimmune disease. Nat Med. 2003;9(1):40-6.
  • 4. Oh CJ, Das KM, Gottlieb AB. Treatment with anti-tumor necrosis factor alpha (TNF-alpha) monoclonal antibody dramatically decreases the clinical activity of psoriasis lesions. J Am Acad Dermatol. 2000;42(5 Pt 1):829-30.
  • 5. Vali A, Asilian A, Khalesi E, Khoddami L, Shahtalebi M, Mohammady M. Evaluation of the efficacy of topical caffeine in the treatment of psoriasis vulgaris. J Dermatolog Treat. 2005;16(4):234-7.
  • 6. Alexandre-Moreira MS, Freire-de-Lima CG, Trindade MN, Castro-Faria-Neto HC, Piuvezam MR, Peçanha LM. Cissampelos sympodialis Eichl (Menispermaceae) leaf extract induces interleukin-10-dependent inhibition of Trypanosoma cruzi killing by macrophages. Braz J Med Biol Res. 2003;36(2):199-205.
  • Address for correspondence:

    Amir Feily
    Jondishapur University of Medical Sciences
    Ahvaz, Iran
    Tel: 00989177204638
    E-mail:
    E-mail:
  • Publication Dates

    • Publication in this collection
      07 Dec 2009
    • Date of issue
      July 2009
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