Polypodium
leucotomos 50:1 standardized extract
Although
the literature on Kalawalla (Polypodium leucotomos
extract) is not limited to all of the trials summarized
below, you can find a compendium of some of the most
important trials that have been carried out with Polypodium
leucotomos extract under its different registered
brands.
TOXICOLOGY
OF POLYPODIUM LEUCOTOMOS EXTRACT (PLE)
Authors: Pablo Cambar+, MD, MSc Pharmacology, University
of Pennsylvania, Danilo Alvarado+, MD, MSc Pathology,
University of Illinois
- Toxicology performed on rats type Wistar, Albino
mice type C3H and rabbits type New Zealand White*.
Lethal Dose 50 (LD50) of PLE intraperithoneal in rats:
LD50 = 2,800 mg / kg, Lethal Dose 50 (LD50) of PLE
intraperithoneal in mice: LD50=3,900 mg / kg
Lethal Dose 50 (LD50) of PLE intraperithoneal in rabbits:
LD50=3,700 mg / kg
Lethal Dose 50 (LD50) of PLE orally in rats: LD50=7000
mg / kg **
Lethal Dose 50 (LD50) of PLE orally in mice: LD50=20,000
mg / kg **
Lethal Dose 50 (LD50) of PLE orally in rabbits: LD50=35,000
mg / kg **
SUB ACCUTE TOXICOLOGY OF PLE
1. Hemathological Parameters Measured (at initial
time, 4 weeks and 12 weeks):
Estrocytes, Leucocytes, Hematocrites, Hemoglobin
2. Biochemical (at initial time, 4 weeks and 12 weeks):
Glucose, Cholesterol, Urea, Creatinine, Total lipids,
TGO, TGP, Total protein, Triglicerids
3. Physical (measured daily):
Water intake, Food intake, Excreted urine, Body weight
- Length of study: 12 weeks
Additional parameters: Blood analyzed taken from the
heart. Once the toxicology was completed, the animals
were sacrificed and the following organs were extracted,
weighed and preserved in formalin for a histopathological
analysis: heart, lungs, liver, kidneys, stomach, suprarhenal,
pancreas, testicles, ovaries, large intestine, small
intestine, bladder.
Results:
No abnormalities or alterations attributed to the
administering of PLE were found.
* Complete toxicology data is fully available for
rats, mice and rabbits.
** This dose is over 1200 times the recommended dose
for a 70 kg adult in a single serving or approximately
1.4 kilos of pure PLE extract (2.8 kilos of PLE powder).
This dose did not provoke the death in any of the
rats, mice or rabbits in the study, rendering the
product completely non toxic when used at suggested
dose.
Anticancer
Res. 2000 May-Jun;20(3A):1567-75. Related Articles,
Links
An extract of the fern Polypodium leucotomos
(Difur) modulates Th1/Th2 cytokines balance in vitro
and appears to exhibit anti-angiogenic activities
in vivo: pathogenic relationships and therapeutic
implications.
Gonzalez
S, Alcaraz MV, Cuevas J, Perez M, Jaen P, Alvarez-Mon
M, Villarrubia VG.
Wellman
Laboratories of Photomedicine, Harvard Medical
School, Boston, MA, USA.
In
the present study we show the capacity of an extract
of the fern Polypodium leucotomos (PLE) to partially
inhibit the production of cytokines showing a Th1
pattern (IL-2, IFN-gamma and TNF-alpha) in human PHA-stimulated
peripheral blood mononuclear cells. The percentage
of inhibition was 24% for IL-2, 72% for INF-gamma
and 53% for TNF-alpha. With regard to Th2 cytokines,
the addition of PLE resulted in a significant increase
(33%) in IL-10 production. Surprisingly, the production
of the inflammatory cytokine IL-6 was completely abolished
(100% inhibition) by PLE at all doses tested.
In a second experiment in vivo we show that, the topical
application of PLE to the skin of hairless albino
mice (Skh-1) significantly diminished the mast cell
infiltrate as well as the number of blood vessels
triggered by chronic ultraviolet B (UVB) irradiation.
These data show that PLE moderately inhibits the immunological
Th1 responses, thus explaining the immunosuppressive
as well as the anti-inflammatory and antioxidant activities
reported in other studies carried out with PLE. The
clear inhibitory effect on TFN-alpha and IL-6 production
strongly suggest that this may be the mechanism by
which PLE: (a) inhibits angiogenesis in vivo in the
mouse model described here, and (b) prevents Langerhans'
cells depletion caused by solar irradiation in humans.
Taken together, these data suggest that PLE works
through the induction of suppressive/anti-inflammatory
cytokines such as IL-10 and/or TGF-beta which in turn
appear to allow the partial deactivation of macrophages
or other accessory cells. These features suggest
that PLE could be useful in the treatment of autoaggressive/inflammatory
conditions due to an exacerbation of Th1 responses.
PMID:
10928072 [PubMed - indexed for MEDLINE]
Immunological
Phenotype and Treatment with Polypodium leucotomos
(Kalawalla) in Multiple Sclerosis (MS) Patients
Spanish
Society of Neurology, XLVI Annual Symposium
MM
Carreño, P Castro, Dept. of Neurology, Navarra
University, Pamplona, Spain
Introduction
and Obejectives
Several studies have shown the existence of abnormal
immunological phenotypes in MS, and more specifically
a imbalance in the suppressor function.
Objectives:
To determine quantitavive abnormalities in the lymphocyte
subpopulation of MS patients, to establish the relationship
with the different clinical pictures and to study
the response to the treatment with an extract of Polypodium
leucotomos.
Patients
and Methods: 12 patients, 10 women and 2 men, with
well established MS; mean age of 43.7 years; evolution
time 6.5 years; treated for one yeat only with an
extract of Polypodium leucotomos (360 – 720
mg / day). The immunological phenotype was studied
counting the lymphocyte sub population.
Statistical
analysis were carried out by non parametric techniques.
Results:
More frequent basal immunological alterations were
increased CD4 in d LB (62.5%), decreased CD8 suppressors
(50%). There was no correlation between the increase
in ICD4 in LB – progressive form and decrease
ICD8 – relapsing / remitting form. The treatment
brought the lymphocyte count to normal in 100% of
the patients with increased CD4 in B. the clinical
evolution, according to the EDSS scale was: Normal
development of course of disease 3 patients (37.5%),
stabilization and improvement 5 patients (62.5%) Increased
in ICD8 suppressor figures were normalized in 3 patients
(50%); worsening was recorder in only 1 patient.
Conclusions
The most frequent immunological alterations of the
phenotype in MS are increase L ind B and decreased
L supp. They are not related to classical forms. The
treatment of Multiple Sclerosis with an extract of
Polypodium leucotomos is useful to correct these phenotype
imbalance and can contribute to a clinical stabilization.
Med Cutan Ibero Lat Am. 1983;11(1):65-72. Related Articles,
Links
2 years personal experience in Anapsos (Polypodium
leucotomos extract) treatment of psoriasis in various
clinical forms
[Article
in Spanish]
Pineiro
Alvarez B.
A
personal experience on 495 patients affected by several
forms of psoriasis and its answer to the treatment
with Anapsos (Polypodium leucotomos extract) is presented.
The whitenings between 80% and 100% of the affected
skin were achieved on 304 patients (61.41%); 46 patients
whitened between 30% and 80% of their lesions, 15
obtained null results and only 11 had relapses. It
is remarkable the high number of abandonments to treatment
which came at 119 patients (24.04%) due to slowness
of process and other reasons probably. The association
with PUVA which shortens the treatment and gives other
advantages is pointed out as positive. The average
time of treatment was 6 months, and daily doses were
from 80 mg. and 720 mg. depending on age, weight and
treatment phase. Side effects appeared in two patients
only: one with intense pruritus and the other one
with gastric disturbances. In both cases, these side
effects disappeared when the treatment was interrupted.
PMID:
6348443 [PubMed - indexed for MEDLINE]
Comments:
Out of 495 patients 93% of those who completed the
6 months treatment with Polypodium leucotomos extract
showed good results.
Vitiligo
repigmentation with Anapsos (Polypodium leucotomos
extract). Mohammad A International journal
of dermatology (1989 Sep), 28(7), 479. Journal code:
0243704. ISSN:0011-9059. Letter written in English.
PubMed ID 2777452 AN 89379534 MEDLINE (Copyright 2004
U.S. National Library of Medicine on SciFinder (R))
Anapsos
(Polypodium leucotomos extract): neuroimmunotrophic
treatment in Alzheimer disease and neurodegenerative
disorders. Alvarez, Anton; Miguel-Hidalgo,
Jose J.; Fernandez-Novoa, Lucia; Diaz, Joaquin; Sempere,
Jose M.; Cacabelos, Ramon. EuroEspes Biomedical Research
Center, Basic and Clinical Neurosciences Research
Center, A Coruna, Spain. CNS Drug Reviews (1997),
3(2), 181-206. CODEN: CDREFB ISSN: 1080-563X. Journal;
General Review written in English. CAN 128:83971 AN
1997:791966 CAPLUS (Copyright 2004 ACS on SciFinder
(R))
Double-blind,
randomized, placebo-controlled pilot study with Anapsos
(Polypodium leucotomos extract) in senile dementia:
effects on cognition, brain bioelectrical activity
and cerebral hemodynamics. Alvarez X A; Pichel
V; Perez P; Laredo M; Corzo D; Zas R; Fernandez-Novoa
L; Sempere J M; Diaz J; Cacabelos R EuroEspes Biomedical
Research Center, A Coruna, Spain. me-direccion@lcg.servicom.es
Methods and findings in experimental and clinical
pharmacology (2000 Sep), 22(7), 585-94. Journal code:
7909595. ISSN:0379-0355. (CLINICAL TRIAL); Journal;
Article; (JOURNAL ARTICLE); (RANDOMIZED CONTROLLED
TRIAL) written in English. PubMed ID 11196347 AN 2001177090
MEDLINE (Copyright 2004 U.S. National Library of Medicine
on SciFinder (R))
Abstract
The
aim of this study was to evaluate the effects of two
doses of Anapsos (Polypodium leucotomos extract) in
comparison with placebo on cognitive performance,
brain bioelectrical activity pattern and cerebral
hemodynamic parameters in patients with mild to moderate
senile dementia of vascular type and Alzheimer type.
Forty-five patients (age 73.8 +/- 7.6 years; range
56-89 years) with mild to moderate senile dementia
(Global Deterioration Scale: stages 3-5) of the vascular
(VD; n = 22) or the Alzheimer type (AD; n = 23) were
included in a double-blind randomized placebo-controlled
clinical trial. After a 2-week period of drug washout,
patients were treated with placebo (n = 15; age 72.7
+/- 7.5 years), 360 mg/day of Anapsos (Polypodium
leucotomos extract) (n = 15; age 75.5 +/- 7.2 years),
or 720 mg/day of Anapsos (Polypodium leucotomos extract)
(n = 15; age 73 +/- 7.7 years) for 4 weeks (28 days).
At baseline and after the 4-week period of double-blind
treatment, cognitive performance, brain bioelectrical
activity power and blood flow hemodynamics in the
middle cerebral arteries were evaluated with ADAScog,
brain mapping and transcranial Doppler ultrasonography,
respectively. Patients receiving 360 mg/day of Anapsos
(Polypodium leucotomos extract) showed a significant
improvement in cognitive performance after treatment
(ADAScog scores: p < 0.05) that was not observed
in patients treated with placebo or 720 mg/day of
Anapsos (Polypodium leucotomos extract). As compared
to placebo, Anapsos (Polypodium leucotomos extract)
(360 mg/day) induced a significant improvement in
ADAScog scores in mild senile dementia patients (p
< 0.01) and in the subset of patients with AD (p
< 0.05). Anapsos (Polypodium leucotomos extract)
(360 mg/day) also increased cerebral blood flow velocities
in left and right middle cerebral arteries in the
subgroup of AD patients, whereas with the dose of
720 mg/kg this increase was only observed in the left
side. Patients treated with Anapsos (Polypodium leucotomos
extract) (360 mg/day) showed a decrease in relative
delta power and an increase in relative theta and
alpha brain bioelectrical activity frequencies, indicating
an acceleration of the EEG pattern.
The present results show that Anapsos (Polypodium
leucotomos extract) (360 mg/day) improves cognitive
performance, cerebral blood perfusion and brain bioelectrical
activity in patients with senile dementia. These effects
of Anapsos (Polypodium leucotomos extract) were more
marked in demented patients with mild mental deterioration
and/or with dementia of the Alzheimer type.
In
vitro studies on the immunomodulating effects of Polypodium
leucotomos extract on human leukocyte fractions.
Brend, A.; Ramirez-Bosca, A.; Huber, H.; Diaz, Alperi,
J.; Thaci, D.; Sewell, A.; Quintanilla, Almagro, E.
Zentrum der Dermatologie und Venerologie, Wolfgang
Goethe-Universitaet, Frankfurt/Main, Germany. Arzneimittel-Forschung
(1995), 45(8), 901-4. CODEN: ARZNAD ISSN: 0004-4172.
Journal written in English. CAN 123:275468 AN 1995:862800
CAPLUS (Copyright 2004 ACS on SciFinder (R))
Abstract
The
in vitro effect of Anapsos (Polypodium leucotomos
extract), a water based ext. of the naturally occurring
fern Polypodium leucotomos (Calagualine), on human
leukocyte fractions was investigated. Calagualine
inhibited interleukin-2 secretion and Con A (Con A)
stimulated proliferation of T-lymphocytes in a concn.-dependent
manner. In contrast, a greatly enhanced secretion
of IL-1a, IL-1? and tumor necrosis factor a was induced
suggesting a stimulation of monocytes and dendritic
cells also present in this system. Endotoxin induced
stimulation was excluded. Also in the absence of Con
A, calagualine stimulated cytokine prodn. The presented
data show for the first time that calagualine exerts
an immunomodulating effect on leukocyte fractions,
paving the way for further detailed studies related
to possible clin. efficacy.
1.
Capella Perez MC, Castells RA. [Double-blind study
using "Polypodium leucotomos" 120 mg. in
the treatment of psoriasis]. Actas Dermosifiliogr
1981;72(9-10):487-494.
Comments: 61 psoriatic patients were treated
for a period of 6 months with Polypodium leucotomos
extract. 90% of the patients showed significant improvement
within this period.
Comparative
study between 120 mg. of Anapsos (Polypodium leucotomos
extract) and a placebo in 37 psoriasis patients. Del
Pino Gamboa J; De Sambricio Guiu F; Colomo Gomez C
Medicina cutanea ibero-latino-americana (1982), 10(3),
203-8. Journal code: 7601805. ISSN:0210-5187. (CLINICAL
TRIAL); (CONTROLLED CLINICAL TRIAL); Journal; Article;
(JOURNAL ARTICLE) written in Spanish. PubMed ID 6759814
AN 83113784 MEDLINE (Copyright 2004 U.S. National
Library of Medicine on SciFinder (R))
Abstract
It
is presented a comparative and clinical study on 37
patients affected by psoriasis, 13 of them took placebo
and 22 finished treatment with Anapsos (Polypodium
leucotomos extract) in capsules of 120 mg. One patient
abandoned treatment by intolerance and another one
with possible laryngeal neoplasm, the drug showed
a discordant result. 9 out of 22 who used Anapsos
(Polypodium leucotomos extract), obtained full whitening,
5 got whitenings between 40% and 80% of the affected
surface, 5 got a maximum of 40% and 3 had null result.
The absence of side effects, minimum intolerance of
product and the amount of obtained successes make
the authors to consider the future of Anapsos (Polypodium
leucotomos extract) optimistically for the treatment
of psoriasis.
Comments:
Most patients treated with Polypodium leucotomos extract
showed significant improvement while placebo patients
did not.
J Am Acad Dermatol. 2004 Jan;50(1):41-9. Related Articles,
Links
Orally administered Polypodium leucotomos
extract decreases psoralen-UVA-induced phototoxicity,
pigmentation, and damage of human skin.
Middelkamp-Hup
MA, Pathak MA, Parrado C, Garcia-Caballero T, Rius-Diaz
F, Fitzpatrick TB, Gonzalez S.
Wellman
Laboratories of Photomedicine, Department of Dermatology,
Massachusetts General Hospital, Harvard Medical School,
Boston 02114, USA.
BACKGROUND:
The use of psoralen-UVA (PUVA) in patients of skin
phototype I to II is limited by side effects of acute
phototoxicity and possible long-term carcinogenesis.
OBJECTIVE: We sought to assess oral Polypodium leucotomos
(PL) extract in decreasing PUVA-induced phototoxicity
of human skin on a clinical and histologic level.
METHODS: A total of 10 healthy patients with skin
phototypes II to III were exposed to PUVA alone (using
0.6 mg/kg oral 8-methoxypsoralen) and to PUVA with
7.5 mg/kg of oral PL. RESULTS: Clinically, phototoxicity
was always lower in PL-treated skin after 48 to 72
hours (P<.005), and pigmentation was also reduced
4 months later. Histologically, PL-treated skin showed
a significant numeric reduction of sunburn cells (P=.05),
preservation of Langerhans cells (P< or =.01),
decrease of tryptase-positive mast cell infiltration
(P<.05), and decrease of vasodilation (P< or
=.01). No differences were found in Ki-67+ proliferating
cells. CONCLUSIONS: PL is an effective chemophotoprotector
against PUVA-induced skin phototoxicity and leads
to substantial benefits of skin protection against
damaging effects of PUVA as evidenced by histology.
PMID:
14699363 [PubMed - indexed for MEDLINE]
Metabolic
effects of calagualine, an antitumoral saponine of
Polypodium leucotomos. Horvath A; Alvarado
F; Szocs J; de Alvardo Z N; Padilla G Nature (1967
Jun 17), 214(94), 1256-8. Journal code: 0410462. ISSN:0028-0836.
Journal; Article; (JOURNAL ARTICLE) written in English.
PubMed ID 6066125 AN 68089646 MEDLINE (Copyright 2004
U.S. National Library of Medicine on SciFinder (R))
Anapsos
(Polypodium leucotomos extract) modifies immunological
parameters and improves the clinical course in atopic
dermatitis. Jimenez D; Doblare E; Naranjo
R; Munoz C; Vargas J F Dermatologica (1986), 173(3),
154-5. Journal code: 0211607. ISSN:0011-9075. (CLINICAL
TRIAL); Letter written in English. PubMed ID 3533665
AN 87031144 MEDLINE (Copyright 2004 U.S. National
Library of Medicine on SciFinder (R))
Anapsos
(Polypodium leucotomos extract), an antipsoriatic
drug, in atopic dermatitis. Jimenez D; Naranjo
R; Doblare E; Munoz C; Vargas J F Departamento de
Dermatologia y Venereologia, Universidad de Granada,
Spain Allergologia et immunopathologia (1987 Jul-Aug),
15(4), 185-9. Journal code: 0370073. ISSN:0301-0546.
Journal; Article; (JOURNAL ARTICLE) written in English.
PubMed ID 2891287 AN 88073810 MEDLINE (Copyright 2004
U.S. National Library of Medicine on SciFinder (R))
Abstract
An
open, controlled study was carried out in young patients
with atopic dermatitis, who during one month received
oral anti-psoriatic drug, Anapsos (Polypodium leucotomos
extract) (n = 46), or antihistamines (n = 30), simultaneously
with topic applications. The activity and extension
of the cutaneous lesions improved under both treatments,
but more markedly with Anapsos (Polypodium leucotomos
extract) in spite of the fact that topical applications
did not contain steroids in the group treated with
Anapsos (Polypodium leucotomos extract), and the effect
was still appreciable several months after interruption
of medication. Anapsos (Polypodium leucotomos extract),
which was well tolerated, considerably relieved the
respiratory symptoms of all patients with asthma.
Studies performed on patients with atopic dermatitis
have shown high IgE levels, eosinophils and T4 counts,
and a marked decrease in T8 suppressor cells in peripheral
blood. Our data also show a slight decrease in T8
cells (%), a significant increase in T4 sub-sets (%)
and a high T4/T8 ratio as a previously reported by
several authors. Such an imbalance between helper
and suppresor cells may cause alterations in the response
to extrinsic and intrinsic antigens, as shown in particular
by the abnormally high IgE levels observed in atopic
dermatitis. Anapsos (Polypodium leucotomos extract)
was associated with a correction in T lymphocytes
imbalances, specifically through the increase of the
initially low T8 cells levels and subsequent normalization
of the mean T4/T8 index. The tolerance and promising
therapeutic activity of this antipsoriatic drug deserve
further research in other conditions characterized
by a deficit of suppressor cells.
Cancer Lett. 2003 Feb 20;190(2):171-82. Related Articles,
Links
Calagualine inhibits nuclear transcription
factors-kappaB activated by various inflammatory and
tumor promoting agents.
Manna
SK, Bueso-Ramos C, Alvarado F, Aggarwal BB.
Cytokine
Research Laboratory, Department of Bioimmunotherapy,
The University of Texas M. D. Anderson Cancer Center,
1515 Holcombe Boulevard, Box 143, Houston, TX 77030,
USA
Calagualine
derived from the fern of the genus Polypodium, commonly
called calaguala, has had clinically documented medicinal
uses in South America and Spain and been shown to
block tumor metastasis, proliferation, and inflammation,
all known to require the activation of nuclear transcription
factor-kappaB (NF-kappaB). Therefore, we investigated
the effect of calagualine on NF-kappaB activation
induced by various inflammatory and tumor promoting
agents. Calagualine blocked tumor necrosis factor
(TNF)-induced activation of NF-kappaB through inhibition
of phosphorylation and degradation of IkappaBalpha,
an inhibitor of NF-kappaB. The effects of calagualine
were not cell type-specific, as it blocked TNF-induced
NF-kappaB activation in a variety of cells. NF-kappaB-dependent
reporter gene transcription activated by TNF was also
suppressed by calagualine. The TNF-induced NF-kappaB
activation cascade involving TNFR1-TNF receptor-associated
death domain-TNF receptor-associated factor 2 (TRAF2)-NF-kappaB-inducing
kinase (NIK)-IkappaBalpha kinase was interrupted at
the TRAF2 and NIK sites by calagualine, which would
account for its suppression of NF-kappaB reporter
gene expression. Calagualine blocked NF-kappaB activation
induced by phorbol ester and lipopolysaccharide. Overall
our results indicate that calagualine inhibits activation
of NF-kappaB and this may provide a molecular basis
for calagualine's ability to suppress inflammation
and tumorigenesis.
PMID:
12565172 [PubMed - indexed for MEDLINE]
Preliminary
communication on the treatment of psoriasis with Anapsos
(Polypodium leucotomos extract).
Mercadal Peyri O; Maesci Cappitanio F Actas dermo-sifilograficas
(1981 Jan-Feb), 72(1-2), 65-8. Journal code: 0373062.
ISSN:0001-7310. Journal; Article; (JOURNAL ARTICLE)
written in Spanish. PubMed ID 7257904 AN 81252352
MEDLINE (Copyright 2004 U.S. National Library of Medicine
on SciFinder (R))
Comments: Most patients
showed significant improvement within the period of
treatment.
Br J Rheumatol. 1998 Aug;37(8):912. Related Articles,
Links
Modification of the inflammatory activity of psoriatic
arthritis in patients treated with extract of Polipodium
leucotomos (Anapsos (Polypodium leucotomos extract))
Navarro-Blasco
FJ, Sempere JM.
Comments:
The use of Polypodium leucotomos proved beneficial
to most patients in the study.
A
new agent (hydrophilic fraction of polypodium leucotomos)
for management of psoriasis. Padilla H C;
Lainez H; Pacheco J A International journal of dermatology
(1974 Sep-Oct), 13(5), 276-82. Journal code: 0243704.
ISSN:0011-9059. (CLINICAL TRIAL); (CONTROLLED CLINICAL
TRIAL); Journal; Article; (JOURNAL ARTICLE) written
in English. PubMed ID 4609374 AN 75035388 MEDLINE
(Copyright 2004 U.S. National Library of Medicine
on SciFinder (R))
Int J Immunopharmacol. 1997 Jan;19(1):9-14. Related
Articles, Links
An extract of the fern Polypodium leucotomos
inhibits human peripheral blood mononuclear cells
proliferation in vitro.
Rayward
J, Villarrubia VG, Guillen C, Prieto A, Rodriguez-Zapata
M, Sada G, Alvarez-Mon M.
Departamento
De Medicina, Hospital Principe De Asturias, Universidad
De Alcala De Henares, Madrid, Spain.
An
alcoholic extract of the fern polypodium leucotomos
(PLE) has been empirically used as an immunosuppressor
for the treatment of several autoimmune diseases.
In this paper, we investigated the effects of PLE
on activation and proliferative responses of peripheral
blood mononuclear cells (PBMNC) from healthy donors
to T lymphocyte polyclonal mitogens. PLE shows a significant
inhibitory effect on the proliferative response of
PBMNC to stimulation with phytohaemagglutinin (PHA)
or anti CD3 monoclonal antibodies (p < 0.05). In
contrast, PLE did not modify the proliferative response
of PBMNC to phorbol esters (p > 0.05). The inhibitory
effect of PLE upon mitogen induced PBMNC proliferation
is time dependent and can be overcome by the exogenous
addition of interleukin-2 to the culture medium (p
< 0.05). The decreased proliferative response of
PBMNC to PHA stimulation in the presence of PLE is
not associated with a significant modification of
expression of the alpha chain (CD25) of the IL-2 receptor
(p > 0.05). In conclusion, PLE shows an inhibitory
effect on the polyclonal proliferative response of
PBMNC to T lymphocyte mitogens that interact with
cytoplasmic membrane molecules.
PMID:
9226474 [PubMed - indexed for MEDLINE]
F. Alvarado, JA Pacheco, PR
Portillo, Z Alvarado, Polypodium leucotomos extract,
an effective treatment against psoriasis. Internal
company document.
Comments: Out of 42 patients treated with
Polypodium leucotomos during a 4 month period, all
of them showed a 75 – 100% clearing of the lesions
within this period.
Effect
of Anapsos (Polypodium leucotomos extract) on in vitro
production of cytokines. Sempere, J. M.;
Rodrigo, C.; Campos, A.; Villalba, J. F.; Diaz, J.
Scientific Dept., ASAC Pharmaceutical International,
Alicante, Spain. British Journal of Clinical Pharmacology
(1997), 43(1), 85-89. CODEN: BCPHBM ISSN: 0306-5251.
Journal written in English. CAN 126:198476 AN 1997:146151
CAPLUS (Copyright 2004 ACS on SciFinder (R))
Abstract
The
aim of the study was to test the immunomodulating
capacity of Anapsos (Polypodium leucotomos extract),
in vitro to explore how this ext. acts from an immunol.
point of view and thus to identify a common link capable
of explaining most of its effects. Polypodium leucotomos
rhizomes were harvested in Guatemala and the ext.,
Anapsos (Polypodium leucotomos extract), obtained.
Mononuclear cells were obtained by d. gradient centrifugation
from healthy donors, and stimulated with phytohemagglutinin
or pokeweed with and without Anapsos (Polypodium leucotomos
extract) and with Anapsos (Polypodium leucotomos extract)
alone. Cell proliferation was detd. by thymidine incorporation.
Cells were also stimulated and the following cytokines
detd. by ELISA at 0, 12, 24, 48, 72, and 96 h: IL-1?,
TNF-?, IL-2, IFN-?, IL-4 and IL-10. Anapsos (Polypodium
leucotomos extract), has a modulating effect on the
in vitro prodn. and release of cytokines by peripheral
blood mononuclear cells of healthy subjects. At doses
effective in vivo, Anapsos (Polypodium leucotomos
extract) can stimulate PBMC proliferation, delay IL-1?
secretion and at the same time increase that of IL-2,
IL-10, and IFN-?. Anapsos (Polypodium leucotomos extract)
may have an antagonistic effect on some of the cytokines
released on cell stimulation with LPS and/or PHA,
which suggests that this product has a pleiotropic
effect on different populations in the immune system.
Anapsos
(Polypodium leucotomos extract), an antipsoriatic
drug which increases the proportion of suppressor
cells in human peripheral blood. Vargas,
J.; Munoz, C.; Osorio, C.; Garcia-Olivares, E. Dep.
Fisiol. Bioquim., Fac. Med., Granada, Spain. Annales
d'Immunologie (Paris) (1983), 134C(3), 393-400. CODEN:
ANIMCZ ISSN: 0300-4910. Journal written in English.
CAN 99:151816 AN 1983:551816 CAPLUS (Copyright 2004
ACS on SciFinder (R))
Abstract
Anapsos
(Polypodium leucotomos extract), an antipsoriatic
drug, was administered to normal volunteers. After
3 days of treatment, the drug decreased the lymphoblastic
response to pokeweed mitogen (PWM) and very slightly
reduced the serum levels of Igs. After 5 days of treatment,
however, both values were normal. The response to
ConA decreased, and there was an increase in the suppressor
index and in the proportion of T-cells of the OKT
8+ subpopulation. The drug did not vary the proportion
of OKT 4+ and OKT 3+ cells. These results suggest
that Anapsos (Polypodium leucotomos extract) acts
by increasing the no. of suppressor cells. Such Anapsos
(Polypodium leucotomos extract)-induced suppressor
cells are probably responsible for the diminished
response to ConA, but did not seem to affect the response
to PWM and serum levels of Ig after 5 days of treatment.
Effects
of calaguala and an active principle, adenosine, on
platelet activating factor. Tuominen, M.;
Bohlin, L.; Rolfsen, W. Dep. Pharmacogn., Uppsala
Univ., Uppsala, Swed. Planta Medica (1992), 58(4),
306-10. CODEN: PLMEAA ISSN: 0032-0943. Journal written
in English. CAN 117:245226 AN 1992:645226 CAPLUS (Copyright
2004 ACS on SciFinder (R))
Abstract
Calaguala,
an ext. from the fern Polypodium decumanum, is used
to treat psoriasis and related immunol. disorders.
The inhibitory activity of the ext. was studied in
2 blood platelet-activating factor (PAF)-related models.
PAF was used to release the proteolytic enzyme elastase
from human neutrophils. Calaguala inhibited this effect
with an IC50 = 0.1 mg/mL. The PAF antagonist ginkgolide
(BN 52021) was used as a pos. control with an IC50
= 0.034 mg/mL. In the second model the inhibition
of PAF biosynthesis in neutrophils was studied using
lyso-PAF and labeled acetyl-CoA. Calaguala showed
a concn.-dependent activity with the IC50 = 0.2 mg/mL.
Since PAF may be involved in the pathogenesis of psoriasis,
the activity of calaguala seen in these PAF assays
may contribute to the clin. efficacy of the ext.
The
flavonoid constituents of two Polypodium species (Calaguala)
and their effect on the elastase release in human
neutrophils. Vasaenge, Mervi; Liu, Boling;
Welch, Christopher J.; Rolfsen, Wenche; Bohlin, Lars.
Division Pharmacognosy, Department Pharmacy, Biomedical
Center, Uppsala University, Uppsala, Swed. Planta
Medica (1997), 63(6), 511-517. CODEN: PLMEAA ISSN:
0032-0943. Journal written in English. CAN 128:119490
AN 1998:2481 CAPLUS (Copyright 2004 ACS on SciFinder
(R))
Abstract
Five
flavonoid compds. were isolated from 2 Polypodium
species (P. decumanum and P. triseriale) with the
common name Calaguala. Structure elucidation was carried
out using different NMR techniques and revealed the
presence of 1 new glycoside (kaempferol 3-O-?-D-xylopyranosyl-(1-2)-?-D-arabinopyranoside)
(I), 2 known flavonoid glycosides, rutin and kaempferol
3-O-?-D-arabinopyranoside, the trimeric proanthocyanidin,
selligueain, and the coumarinic acid deriv., melilotoside.
The compds. were tested for their activity in platelet
activating factor (PAF) induced exocytosis in human
neutrophils but none of the compds. showed PAF specific
activity. Instead, they showed more general effects
on the neutrophil including inhibition of the spontaneous
elastase release (melilotoside) and potentiation of
the release induced by PAF I. Selligueain inhibited
the proteolytic enzyme, elastase in vitro.
A
sulphonoglycolipid from the fern Polypodium decumanum
and its effect on the platelet activating-factor receptor
in human neutrophils. Vasange M; Rolfsen
W; Bohlin L Department of Pharmacy, Uppsala University,
Sweden Journal of pharmacy and pharmacology (1997
May), 49(5), 562-6. Journal code: 0376363. ISSN:0022-3573.
Journal; Article; (JOURNAL ARTICLE) written in English.
PubMed ID 9178195 AN 97321474 MEDLINE (Copyright 2004
U.S. National Library of Medicine on SciFinder (R))
Abstract
The
South American fern Polypodium decumanum, traditional
name calaguala, has documented clinical use in oral
treatment of skin disorders, including psoriasis.
The inflammatory mediator platelet-activating factor
(PAF), has been implicated in the pathogenesis of
psoriasis. A constituent of a calaguala extract has
been shown to have inhibitory activity in a PAF-induced
exocytosis model in human neutrophils. The compound
was identified as the sulphoquinovosyl diacylglycerol
1,2-di-O-palmitoyl-3-O-(6-sulpho-alpha-D-quinovopyranosyl)-glycero
l by spectroscopic means. When subsequently studied
in an in-vitro model for [3H]PAF binding in neutrophils
from man the compound caused dose-dependent displacement
of [3H]PAF from its receptor with an IC50 value of
2 microM. It is suggested that the compound acts through
PAF receptor antagonism in intact human neutrophils.
The
fern Polypodium decumanum, used in the treatment of
psoriasis, and its fatty acid constituents as inhibitors
of leukotriene B4 formation. Vasange-Tuominen,
M.; Perera-Ivarsson, P.; Shen, J.; Bohlin, L.; Rolfsen,
W. Dep. Pharm., Uppsala, Swed. Prostaglandins, Leukotrienes
and Essential Fatty Acids (1994), 50(5), 279-84. CODEN:
PLEAEU ISSN: 0952-3278. Journal written in English.
CAN 120:315432 AN 1994:315432 CAPLUS (Copyright 2004
ACS on SciFinder (R))
Abstract
The
fern P. decumanum, commonly called Calaguala, has
a clin. documented use in South America and Spain
in the treatment of psoriasis. One of the inflammatory
mediators isolated in abnormally high quantities in
the psoriatic skin is leukotriene B4 (LTB4). Calaguala
was tested in an in vitro model using human leukocytes
for its ability to inhibit the LTB4 formation. The
inhibition was found to be caused by the polyunsatd.
fatty acids (PUFAs) linoleic, linolenic and arachidonic
acid. IC50 values were detd. for the isolated acids
and compared to a group of closely related acids also
commonly found in nature. IC50 values for most acids
tested were of the same magnitude (20-60 ?M) except
for arachidonic acid which showed stimulatory activity
and 8-(R)-hydroxylinoleic acid which gave 30% inhibition
with the highest dose tested (120 ?M). The amts. of
PUFAs in different Calaguala ext. were quant. analyzed
and it is concluded that the fatty acid constituents
of Calaguala may contribute to the clin. effects of
the ext.
Quantitative
determination of antiinflammatory principles in some
Polypodium species as a basis for standardization.
Liu, B.; Diaz, F.; Bohlin, L.; Vasaenge, M. Div. Pharmacognosy,
Dep. Pharmacy, Biomedical Center, Uppsala Univ., Uppsala,
Swed. Phytomedicine (1998), 5(3), 187-194. CODEN:
PYTOEY ISSN: 0944-7113. Journal written in English.
CAN 129:140525 AN 1998:371470 CAPLUS (Copyright 2004
ACS on SciFinder (R))
Abstract
Polyunsatd.
fatty acids (linoleic, linolenic, arachidonic acid),
the triflavonoid selligueain, and a sulfonoglycolipid
(SQDG) were detd. quant. by high-performance liq.
chromatog. in the leaves and rhizomes of 5 Polypodium
species (Calaguala). Exts. of the 5 ferns were studied
in 3 in vitro bioassays using platelet activating
factor and leukotriene B4. SQDG was present in pharmacol.
detectable amts. in the crude exts. The anal. method
for quant. detn. of SQDG was recommended to be used
for standardization of Calaguala ext. in herbal drug
prepns.
Therapeutic
properties of Polypodium angustifolium (Calahuala).
Pareja, Bertha; et al. Fac. Farm. Bioquim., Univ.
Nac. Mayor San Marcos, Lima, Peru. Boletin de la Sociedad
Quimica del Peru (1988), 54(2), 89-95. CODEN: BSQPAQ
ISSN: 0037-8623. Journal written in Spanish. CAN 111:219163
AN 1989:619163 CAPLUS (Copyright 2004 ACS on SciFinder
(R))
Abstract
Calahuala
is a folk medicine, derived from the fern P. angustifolium,
which is used in South America as an anti-inflammatory
prepn. and for other purposes. Anal. of an EtOH ext.
of the leaves of this plant indicates that the active
component of Calahuala is an anthraquinone which may
be suitable for use as a starting material for synthesis
of corticosteroid hormones.
J Photochem Photobiol B. 2003 Apr;70(1):31-7. Related
Articles, Links
Photoprotective properties of a hydrophilic
extract of the fern Polypodium leucotomos on human
skin cells.
Alonso-Lebrero
JL, Dominguez-Jimenez C, Tejedor R, Brieva A, Pivel
JP.
R&D
Department, Industrial Farmaceutica Cantabria S.A.,
Madrid, Spain.
The
effect of a hydrophilic extract of the fern Polypodium
leucotomos (PLE) has been investigated in terms of
photoprotection against UV-induced cell damage. PLE
efficiently preserved human fibroblast survival and
restored their proliferative capability when the cells
were exposed to UVA light. This effect was specific
and dose-dependent. Photoprotection was not restricted
to fibroblasts, as demonstrated by its effect on survival
and proliferation of the human keratinocyte cell line
HaCat. Finally, treatment of the cells with PLE prevented
UV-induced morphological changes in human fibroblasts,
namely disorganisation of F-actin-based cytoskeletal
structures, coalescence of the tubulin cytoskeleton
and mislocalization of adhesion molecules such as
cadherins and integrins. Our in vitro results demonstrate
the photoprotective effect of PLE on human cells and
support its use in the preventive treatment of sunburning
and skin pathologies associated with UV-mediated damage.
PMID:
12745244 [PubMed - indexed for MEDLINE]
T. Hornedo, Inigo, JM Belmar,
Clinical assay on 44 psoriatic patients using Polypodium
leucotomos extract. Antol. Dermat. No. 1 (52 –
55), Jan 1983
Comments: 80% of the patients treated obtained
good results within 2 – 5 months of use.
Internal
Company Statistics. Out of a 3 year study
on Organic Hope patients and their satisfaction with
Polypodium leucotomos for the treatment of different
types of psoriasis, 95% of all patients showed complete
satisfaction within 6 months of use of Kalawalla.
Internal
Company Research: There is no toxicity associated
with the short or long term use of Polypodium leucotomos
extract. Side effects reported: upset stomach (less
than 5 in 1,000 patients). Interactions: HBP lowering
medications. Polypodium leucotomos theoretical reduces
HBP, hence producing an unsafe decrease in BP when
combined with HBP medications. Other supplements with
similar BP lowering effects.
