| (84) |
Designated Contracting States: |
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AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO
PL PT RO SE SI SK TR |
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Designated Extension States: |
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RS |
| (30) |
Priority: |
02.04.2008 IT MI20080567
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| (43) |
Date of publication of application: |
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08.12.2010 Bulletin 2010/49 |
| (73) |
Proprietor: Androsystems S.R.L. |
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00198 Roma (IT) |
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| (72) |
Inventor: |
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- GRECO, Ermanno
I-00198 Roma (IT)
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| (74) |
Representative: Modiano, Micaela Nadia et al |
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Modiano & Partners (IT)
Via Meravigli, 16 20123 Milano 20123 Milano (IT) |
| (56) |
References cited: :
WO-A-2006/002096 WO-A-2007/114903
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WO-A-2006/113389
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- DREWES S E ET AL: "Recent findings on natural products with erectile-dysfunction activity"
PHYTOCHEMISTRY, PERGAMON PRESS, GB, vol. 62, no. 7, 1 April 2003 (2003-04-01), pages
1019-1025, XP004410106 ISSN: 0031-9422
- DURACKOVA Z ET AL: "Lipid metabolism and erectile function improvement by Pycnogenol,
extract from the Pinus pinaster in patients suffering from erectile dysfunction-a
pilot study" NUTRITION RESEARCH, ELSEVIER INC, XX, vol. 23, no. 9, 1 September 2003
(2003-09-01), pages 1189-1198, XP002983608 ISSN: 0271-5317
- SOMMER F ET AL: "Evaluation of tetrahydrobiopterin (BH4) as a potential therapeutic
agent to treat erectile dysfunction" ASIAN JOURNAL OF ANDROLOGY, SCIENCE PRESS, SHANGHAI,
CN, vol. 8, no. 2, 1 March 2006 (2006-03-01), pages 159-167, XP008107947 ISSN: 1008-682X
- DUMITRESCU CRISTIAN ET AL: "Tetrahydrobiopterin and NADPH treatment reverses endothelial
dysfunction in post-ischemic hearts" CIRCULATION; 77TH SCIENTIFIC MEETING OF THE AMERICAN-HEART-ASSOCIATI
ON, NOVEMBER 07-10, 2004, LIPPINCOTT WILLIAMS & WILKINS, US; NEW ORLEANS, LA, USA,
vol. 110, no. 17, suppl. S, 26 October 2004 (2004-10-26), page 206, XP008107792 ISSN:
0009-7322
- TENORIO F A ET AL: "Vasodilator activity of the aqueous extract of Viscum album" FITOTERAPIA,
IDB HOLDING, MILAN, IT, vol. 76, no. 2, 1 March 2005 (2005-03-01), pages 204-209,
XP025264959 ISSN: 0367-326X [retrieved on 2005-03-01]
- TODA N ET AL: "Nitric oxide and penile erectile function" PHARMACOLOGY AND THERAPEUTICS,
ELSEVIER, GB, vol. 106, no. 2, 1 May 2005 (2005-05-01), pages 233-266, XP004870345
ISSN: 0163-7258
- SULLIVAN M E ET AL: "Nitric oxide and penile erection: is erectile dysfunction another
manifestation of vascular disease?" CARDIOVASCULAR RESEARCH 15 AUG 1999, vol. 43,
no. 3, 15 August 1999 (1999-08-15), pages 658-665, XP002535884 ISSN: 0008-6363
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Remarks: |
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The file contains technical information submitted after the application was filed
and not included in this specification |
|
Technical field
[0001] The present invention relates to L-citrulline at a dose equal to 6 g/day and its
pharmaceutical composition for treating erectile dysfunction.
Background art
[0002] It is now universally acknowledged that endothelial dysfunction, an alteration of
the normal biochemical processes normally performed by endothelial tissue which causes
several vascular disorders and particularly male erectile dysfunction, is due to the
reduced local bioavailability of nitric oxide (NO), the quintessential endogenous
vasodilatory substance.
[0003] Production of nitric oxide occurs starting from a semi-essential amino acid, L-arginine,
which is converted into nitric oxide and citrulline by the nitric oxide synthase (NOS)
enzyme. There are three isoforms of this enzyme, designated respectively by the acronyms
NOS1 (neuronal), NOS2 (inducible) and NOS3 (endothelial).
[0004] Nitric oxide, once produced, enters the smooth muscle cell, where it activates a
particular enzyme known as soluble guanylyl cyclase (sGC), with a consequent increase
in the quantity of intracellular cyclic guanosine monophosphate (cGMP), reduction
in the concentration of Ca
2+ ion, and consequent vasodilation.
[0005] In view of the above, there are three hypothetical ways to act on the decrease in
nitric oxide bioavailability: increase the bioavailability of the nitric oxide precursor,
i.e., L-arginine; increase the activity of NOS enzymes; and increase the concentration
of intracellular cGMP.
[0006] The semi-essential amino acid L-arginine is derived mostly from food and only for
5-15% from de novo synthesis. Several metabolic studies have shown that after oral
administration, L-arginine is subjected to massive systemic and pre-systemic elimination
by intestinal bacteria and by the arginases present in the intestine and liver. A
recent experimental study, in which a radioactive isotope of L-arginine was administered,
showed that only 1% of the administered dosage is used as a precursor by NOS, mostly
due to intense intestinal metabolism. Moreover, it has been demonstrated scientifically
that the administration of L-arginine produces blood levels of this amino acid that
are characterized by a short half-life, a factor which severely limits the possibility
of L-arginine to perform a satisfactory therapeutic effect. Another limitation to
oral administration of high doses of L-arginine is the presence of endogenous inhibitors
of the reaction for conversion of L-arginine into nitric oxide by NOS. These inhibitors
push the activity curve of the enzyme reaction toward higher levels of L-arginine
than those administered, an effect acknowledged scientifically as a "paradox effect".
[0007] Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of all three NOS isoforms.
ADMA normally circulates in blood at low dosages, but a conspicuous increase thereof
is observed in subjects affected by endothelial dysfunction and in particular by erectile
dysfunction or in subjects receiving excessive administration of L-arginine. It has
been demonstrated scientifically that the ratio between L-arginine and ADMA is one
of the key factors in the production of nitric oxide by NOS.
[0008] Accordingly, oral administration of L-arginine is unable to increase endogenous production
of nitric oxide due to the low absorption of this amino acid caused by: the intense
catabolism to which it is subjected in the intestine; its short half-life; and difficulty
in modifying the L-arginine/ADMA ratio.
[0009] Currently, erectile dysfunction therapy is based substantially on oral administration
of phosphodiesterase-5 (PDE5) inhibitors. Drugs containing active ingredients capable
of inhibiting PDE5 act by increasing the bioavailability of cGMP at the smooth muscle
cell level, inhibiting its catabolism operated by PDE5. However, these drugs are actually
unable to increase nitric oxide synthesis and are therefore considered "on demand"
drugs, which lead to a temporary increase in erectile functionality.
[0010] WO 2006/002096 disclosed L-citrulline as a sole agent for the treatment of erectile dysfunction.
The dosage of L-citrulline was up to 3 g per day.
[0011] As an alternative, therapies are being tested for treating erectile dysfunction by
direct insertion of the NOS gene at the penile endothelial cell level. This gene therapy
procedure uses bacterial vectors to transfer the NOS gene and up to now has proved
to be valid in improving erectile function in rats. However, such a method has not
yet been developed sufficiently for use in humans; moreover, resorting to gene therapy
procedures, and in particular the use of bacterial vectors, is an approach that might
be more difficult to accept for a patient with respect to the administration of a
drug.
[0012] There is, therefore, the need for a drug that can cure erectile dysfunction by increasing
the amount of nitric oxide produced by the body.
Disclosure of the Invention
[0013] The aim of the present invention is to provide a drug that can cure erectile dysfunction
wherever it occurs by means of an increase in the endogenous production of nitric
oxide and does not require ad hoc administration to obtain a momentary increase in
nitric oxide.
[0014] Within this aim, an object of the invention is to provide a drug that is capable
of acting in a differentiated but simultaneous manner on the normal biochemical processes
that regulate endogenous synthesis of nitric oxide.
[0015] Another object of the invention is to provide a drug that leads to an increase in
the bioavailability of L-arginine.
[0016] Still another object of the present invention is to provide a drug that can induce
nitric oxide synthase (NOS) activity.
[0017] Finally, an object of the present invention is to provide a drug that can increase
the penetration of L-arginine at the endothelial intracellular level.
[0018] Other objects, characteristics and advantages of the invention will be described
in the foregoing detailed description.
[0019] This aim and these and other objects that will become better apparent hereinafter
are achieved by L-citrulline for the treatment of erectile dysfunction.
[0020] The aim and objects of the invention are also achieved by a pharmaceutical composition
comprising L-citrulline in combination with one or more substances selected from the
group consisting of, aqueous extract of
Viscum album and nicotinamide adenine dinucleotide phosphate (NADPH).
Ways of carrying out the invention
[0021] Without intending to be bound to any theory in particular, it is believed that the
therapeutic action of L-citrulline in the treatment of endothelial dysfunction is
due to the fact that this non-essential amino acid does not undergo pre-systemic elimination.
It is in fact believed that L-citrulline undergoes systemic metabolism, during which
it is converted by the L-argininosuccinate synthase enzyme into L-argininosuccinate,
which in turn is broken down by the L-argininosuccinase enzyme to yield L-arginine.
From this point of view, L-citrulline can be considered as the natural precursor of
L-arginine. L-citrulline in fact allows indirectly to increase the bioavailability
and plasma half-life of L-arginine, since differently from L-arginine it does not
undergo intense intestinal catabolism.
[0022] The inventor of the present invention has thus discovered that the administration
of L-citrulline, at a dose equal to 6 g/day, is capable of curing erectile dysfunction.
[0023] Another embodiment of the present invention consists of the further combination of
L-citrulline for the treatment of erectile dysfunction with aqueous extract of
Viscum album.
[0024] Viscum album is a plant known by the more common name of mistletoe. The aqueous extract of this
plant has proved to be capable of inducing an overexpression of NOS2 and NOS3 enzymes
at the level of muscle cells of the Guinea pigs to which it has been administered.
[0025] The inventor of the present invention has discovered that resorting to a combination
of L-citrulline with
Viscum album extract allows to increase the quantity and activity of endogenous NOS, with a consequent
higher production of nitric oxide.
[0026] Another embodiment of the present invention also consists of the further combination
of L-citrulline for the treatment of erectile dysfunction with nicotinamide adenine
dinucleotide phosphate (NADPH).
[0027] Enzyme cofactors such as NADPH are substances whose presence is required for the
optimum biochemical activity of some enzymes. In particular, in the case of the reaction
for production of nitric oxide from L-arginine, NOS enzymes use NADPH and tetrahydrobiopterin
as essential cofactors.
[0028] The inventor of the present invention has discovered that resorting to a combination
of L-citrulline with NADPH allows to favor the activity of NOS and accordingly the
production of nitric oxide.
[0029] Moreover, it is known that the rise of blood levels of homocysteine reduces endothelial
penetration of L-arginine and that in a patient with erectile dysfunction, blood levels
of homocysteine increase. Folic acid, a cofactor of the enzymes involved in the synthesis
of homocysteine, has a specific action in lowering the values of homocysteine.
[0030] Therefore, in an embodiment of the present invention, L-citrulline on its own or
in combination with one or more substances selected from the group consisting of aqueous
extract of
Viscum album and NADPH can be characterized in that the treatment of the erectile dysfunction
occurs by means of the simultaneous increase in the levels of L-arginine and nitric
oxide synthase (NOS).
[0031] In an embodiment of the present invention, L-citrulline is administered in a quantity
equal to 6 grams/day. For example, daily administration of L-citrulline may be split
into two doses of 3 grams each or three doses of 2 grams each.
[0032] Moreover, L-citrulline for treating erectile dysfunction may be used also in combination
with other drugs already known for treatment of erectile dysfunction, for example
drugs containing PDE5 inhibitors.
[0033] In another aspect, the present invention relates also to a pharmaceutical composition
characterized in that it comprises L-citrulline in combination with one or more substances
selected from the group consisting of aqueous extract of
Viscum album and NADPH.
[0034] Of course, the pharmaceutical composition of the present invention may further comprise
one or more excipients generally used in pharmaceutical practice.
[0035] Moreover, the composition may assume any formulation suitable for its administration
to a patient affected by erectile dysfunction. For example, the composition according
to the invention may be in the form of powder, capsules or sachets.
[0036] The inventor of the present invention has discovered that the pharmaceutical composition
described herein is effective particularly in the treatment of erectile dysfunction,
and therefore in a preferred embodiment the pharmaceutical composition according to
the invention may be used in the treatment of erectile dysfunction.
[0037] The present invention relates to treating erectile dysfunction by administering L-citrulline
to a patient, optionally in combination with one or more substances selected from
the group consisting of aqueous extract of
Viscum album and NADPH.
[0038] Preferably, the method according to the invention may provide for oral administration
of L-citrulline.
[0039] Moreover, in the method according to the invention L-citrulline is administered in
an amount equal to 6 grams/day. For example, the daily administration of L-citrulline
may be split into two doses of 3 grams each or three doses of 2 grams each.
[0040] The effectiveness of the administration of L-citrulline in the treatment of erectile
dysfunction has been verified by conducting a randomized prospective study on 20 patients,
during which L-citrulline was administered orally with a dosage of 6 grams/day, in
two separate 3-gram doses, to patients affected by erectile dysfunction. As a comparison,
a second group of patients received an administration of L-arginine equal to 3 grams/day,
split into two 1.5-gram doses.
[0041] The effects of the administration were then tested at the biochemical level by studying
the following parameters:
- 1. plasma levels of L-arginine;
- 2. blood modification of L-arginine/ADMA ratio;
- 3. urinary excretion of nitrates;
- 4. urinary excretion of cGMP.
[0042] Moreover, the effects at the clinical level were also tested by administering the
"Erectile function assessment card" (IIF-5 questionnaire) to the patients and by measuring
flow-mediated vasodilation of the cavernous arteries before and after therapy.
[0043] The data related to the above cited biochemical parameters were acquired for patients
subjected to the test 7 days after the beginning of the administration of the drug
and are shown below in Table 1, Table 2, Table 3 and Table 4.
Table 1
| Plasma levels of L-arginine (µmol/l) |
| Drug |
Max plasma concentration |
| L-arginine |
89 ± 10 |
| L-citrulline |
172 ± 25 |
Table 2
| L-arginine/ADMA ratio |
| Drug |
baseline |
after administration |
| |
|
|
| L-arginine |
186 ± 7 |
189 ± 10 |
| L-citrulline |
183 ± 8 |
290 ± 15 |
Table 3
| Urinary excretion of nitrates (nmol/mmol creatinine) |
| Drug |
baseline |
after administration |
| L-arginine |
91 ± 10 |
93 ± 12 |
| L-citrulline |
89 ± 9 |
133 ± 16 |
Table 4
| Urinary excretion of cGMP (nmol/mmol creatinine) |
| Drug |
baseline |
after administration |
| L-arginine |
38 ± 3.1 |
39 ± 4.5 |
| L-citrulline |
40 ± 2.8 |
55 ± 3.8 |
[0044] The data shown in Tables 1 to 4 allow to observe that oral administration of L-citrulline,
with respect to the administration of L-arginine, is able to produce statistically
higher plasma levels of arginine and to lead to a statistically longer plasma half-life
of L-arginine. Moreover, it should be noted that the administration of L-citrulline
also leads to a higher excretion of nitrates and cGMP (measured in terms of nmol/mmol
of creatinine), a sign of actual production of nitric oxide by endothelial tissues.
[0045] Moreover, from a clinical standpoint, it has been observed that administration of
L-citrulline leads to a modification of the IIF-5 questionnaire by patients at the
level of the components related to achieving and maintaining erection. Also from a
clinical standpoint, a statistically higher increase in flow-mediated vasodilation
at the level of the cavernous arteries was also observed with administration of L-citrulline.
[0046] In practice it has been found that L-citrulline for treating erectile dysfunction
according to the invention fully achieves the intended aim, since the administration
of L-citrulline alone at a dose equal to 6 g/day modifies positively and in a statistically
significant way the biochemical and clinical parameters linked to erectile dysfunction,
thus indicating that the endogenous capacity of tissues to synthesize nitric oxide
has been restored.
[0047] Moreover, it has been observed that L-citrulline at a dose equal to 6 g/day, also
thanks to combination with other substances such as extract of
Viscum album and NADPH allows to act in a differentiated but simultaneous manner on the normal
biochemical processes that regulate endogenous synthesis of nitric oxide.
[0048] It has in fact been observed that L-citrulline alone at a dose equal to 6 g/day or
in combination with extract of
Viscum album and/or NADPH allows to increase the bioavailability of L-arginine, induce the activity
of NOS enzymes and increase the penetration of L-arginine at the endothelial intracellular
level.