"Afrin" cure?

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"Afrin" cure?

Postby Artist » Tue Nov 27, 2007 5:46 pm

OK, maybe not a "cure", but this is impressive. Anyone tried "Afrin" topically before? I've always been afraid of "rebound dilation", but they addressed this concern in the study, and it looks as though it doesn't happen...if their observations are correct. Only two people, so really just a case study, but they were followed for eight and 17 months and no evidence of rebound or problems, evidently. They applied an over-the-counter Oxymetazoline HCL solution to their rosacea once daily. An example is "Afrin" nasal spray.

"At the last follow-up examination, patient 1 had continued treatment for 8 months and patient 2 for 17 months, with sustained effects. Both patients had discontinued all other therapies directed toward their rosacea other than sunscreen use." (From below study)

I do wonder if there is systemic absorption when used on the skin. I imagine if used on the skin, and on such a small area, that systemic absorption would be negligible, but a doctor's advice would be prudent - especially if you have high blood pressure or any of the contraindicated conditions listed. I think I'll try a little test spot. I have Afrin in my medicine cabinet. Comments? -Artist

--------------


Successful Treatment of the Erythema and Flushing of Rosacea Using a Topically Applied Selective {alpha}1-Adrenergic Receptor Agonist, Oxymetazoline

Stuart D. Shanler, MD; Andrew L. Ondo, MD
School of Medicine, University of New Mexico, Albuquerque (Dr Ondo). Dr Shanler is in private practice in New York, New York.

Arch Dermatol. 2007;143(11):1369-1371.

INTRODUCTION


The erythematotelangiectatic (ETR) subtype of rosacea is characterized by frequent episodes of facial flushing and persistent centrofacial erythema and may be accompanied by telangiectasias, facial edema, burning, or stinging. The pathophysiologic cause of the erythema is uncertain, and there are currently no satisfactory treatments for this common form of rosacea.


REPORT OF CASES


CASE 1

A 55-year-old man presented with a long history of ETR rosacea manifesting with prolonged facial flushing provoked by multiple stimuli including heat, exercise, sun exposure, and the consumption of alcoholic beverages. He confided that he was particularly disturbed that, for many years, people frequently asked him: "Why is your face so red?" His condition had progressed over the last 15 years to include persistent facial erythema. In addition to his usual triggers, he had noted that during his workday in an air conditioned office the erythema worsened, usually peaking in early afternoon, sometimes with concurrent facial stinging or burning. He had previously been treated with several oral antibiotics, multiple topical therapies including metronidazole, and most recently azelaic acid gel, with no effect. He asked if there was anything that might help the erythema and symptoms.

CASE 2

A 70-year-old woman presented with a history of ETR rosacea, progressively worsening throughout her adult life. Although she had endured episodic flushing for decades, her erythema had become persistent in recent years. She had used numerous topical antibiotics for decades, including metronidazole, clindamycin phosphate, and combination sodium sulfacetamide, 10%, and precipitated sulfur, 5%, in an attempt to alleviate the erythema. She noted no improvement with the use of any of these agents and stated that she had continued using them "more out of hope" than because the medications had any effect. She had also used topical tretinoin with no improvement and had considered pulsed-dye laser therapy but had decided against it.


THERAPEUTIC CHALLENGE




Erythematotelangiectatic rosacea, in general, responds poorly to treatment. Topical and oral antibiotics, standard treatment for papulopustular rosacea, are usually ineffective. Oral systemic agents such as beta-blockers, clonidine hydrochloride, and spironolactone have little evidence of benefit; these agents also have potential systemic adverse effects. The pulsed-dye laser and, more recently, other nonablative laser and light therapies have been used to treat erythema and telangiectasias; however, not all patients respond, multiple treatment sessions are required, recurrences are common, costs can be significant, and flushing is often persistent. Our 2 patients demonstrate typical features of ETR rosacea with easily triggered, treatment resistant, socially embarrassing, persistent facial erythema and discomfort (stinging and burning). Neither patient demonstrated a papulopustular component, phymatous component, or ocular component to their disease, and conventional therapeutic options had not been effective.


SOLUTION


An attempt to treat ETR rosacea using an over-the-counter drug known to possess vasoconstrictive properties was undertaken. A commercially available preparation of oxymetazoline hydrochloride, 0.05%, solution was applied once daily to the affected area of the face.

Patient 1 and her physician (1 of us) (A.L.O.) noted a decrease in facial erythema within 1 hour of drug application, and a dramatic improvement within 2 to 3 hours. This effect was sustained throughout the entire day. After a 7:30 AM application of the drug, the patient noted an improvement in the chronic "baseline" erythema, and experienced a marked reduction in his transient flares. His erythema continued to be controlled in the early afternoon, at his normal time of peak erythema, and he experienced no stinging or burning (Figure).


Figure 1
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Figure. Baseline photograph of patient 1 immediately prior to application of oxymetazoline, 0.05%, solution (A) and 3 hours after topical application (B), demonstrating marked improvement in macular erythema and fine telangiectasias.


Patient 2 reported a similar improvement in her appearance and symptoms. Two weeks after initiating therapy, she was so pleased with the response that she sent her physician (1 of us) (A.L.O.) a letter of thanks indicating that the treatment was still effective and that she had discontinued use of topical metronidazole, her most current treatment. She returned 3 months after initiating therapy and continued to evidence marked improvement in the erythema and had experienced no episodic flares or flushing.

Both patients were counseled that this treatment was "off label" and that even though the medication was over the counter, adverse effects could occur and could include the listed adverse effects of underlying heart disease, hypertension, thyroid disease, diabetes mellitus, and urinary retention. Both patients elected to continue treatment on their own. Patient 1 stated that "This is the first time my face has been normal in decades." Six weeks after initiating once-daily application, patient 1 demonstrated continued control of the erythema and had complete relief of his facial stinging and burning. Neither patient experienced any adverse effects, has evidenced any rebound flares in erythema or other symptoms, or has demonstrated any tachyphylaxis to the current regimen. At the last follow-up examination, patient 1 had continued treatment for 8 months and patient 2 for 17 months, with sustained effects. Both patients had discontinued all other therapies directed toward their rosacea other than sunscreen use.


COMMENT


Rosacea is a common, chronic cutaneous disorder, the clinical manifestations and subtypes of which have been very well described and recently reviewed.1-3 Erythematotelangiectatic rosacea is the subtype of rosacea most characterized by its frequent episodes of transient facial erythema (flushing) and nontransient, or persistent, erythema. It may be accompanied by facial edema, burning, or stinging.3 While rosacea remains a disorder of uncertain etiology and pathogenesis, the abnormal flushing and persistent erythema have usually been theorized to arise from a dysregulation in the cutaneous vasomotor response, which, whether triggered by neurogenic, hormonal, thermal, topical, or other stimuli, has as its end result an abnormal and persistent dilation of facial blood vessels.1-2,4-7

The regulation of the cutaneous circulation is of paramount importance and is extremely complex. It is mediated by the sympathetic nervous system both locally, through the release of catecholamines from the sympathetic nerve terminals, and systemically, through their release into the general circulation by the adrenal medulla. In recent years, and with newer molecular genetic techniques, the simple model of 2 adrenergic receptors (adrenoceptors) that mediate the vascular response to catecholamines8 has been replaced. The concept of "generic" {alpha}-adrenergic receptors, responsible mostly for "excitatory" functions such as vasoconstriction and uterine and urethral contraction, and "generic" beta-adrenergic receptors, responsible mostly for "inhibitory" functions such as vasodilatation, bronchodilation, and uterine and urethral relaxation (though notably inotropic for the heart) has been further refined and specific receptor subtypes, localizations, and functions have been elucidated. The current model is that of a complex family of structurally related receptors consisting of at least 6 {alpha}-receptor subtypes ({alpha}1A [{alpha}1a/c], {alpha}1B, {alpha}1D, {alpha}2A [{alpha}2A/D], {alpha}2B, and {alpha}2C) and at least 3 beta-receptor subtypes (beta1, beta2, and beta3),9-13 with additional conformational variants such as {alpha}1L and beta4 bringing the total number of functional adrenoceptor conformations to at least 11.

These adrenergic receptors are all members of the G-protein–coupled receptor superfamily of proteins and modulate their effects through a classic 7-transmembrane protein second-messenger system. Their final local and systemic effects, however, are myriad, as noted previously, including vasoactive effects ranging from vasoconstriction to vasodilatation, and occur through a wide variety of intracellular mechanisms12 that are governed by local receptor subtype concentration, relative receptor subtype distribution throughout the body, ligand-binding characteristics, and other factors (eg, local temperature and hypoxia), the full discussion of which is beyond the scope of this article.9-14 Elegant in vitro, in vivo, and ex vivo studies in a variety of vascular tissues and species reveal that the contraction of peripheral vascular smooth muscle is primarily mediated by {alpha}1A- and {alpha}1D-receptor subtypes, although it varies in different vascular regions.10-11,15 Studies of {alpha}2-receptor suggest that {alpha}2A/D and {alpha}2B effects are also of importance, particularly on the arterial side, and that the {alpha}2A/D and {alpha}2C effects are of importance on the venular side, although variations based on the experimental model used are well reported.10-13,15 The actual physiologic and clinical responses to stimulating or inhibiting these receptors selectively is, however, difficult to predict.

Oxymetazoline is a synthetic, direct-acting, imidazoline-type sympathomimetic agonist that is highly selective for the {alpha}1A-adrenoceptor and is a partially selective {alpha}2A-receptor agonist as well. It is a potent vasoconstrictor. Locally applied {alpha}1-adrenoreceptor agonists such as phenylephrine hydrochloride, naphazoline hydrochloride, tetrahydrozaline hydrochloride, oxymetazoline hydrochloride, and xylometazoline hydrochloride are well known for their ability to clinically "get the red out" and have been used as vasoconstrictive agents in over-the-counter preparations for decades. These drugs have been used as decongestants on nasal and ocular mucous membranes for the treatment of conditions such as allergic rhinitis and conjunctivitis and decrease erythema and edema of the mucous membranes with safety and excellent efficacy. Selective {alpha}2-adrenoceptor agonists such as brimonidine tartrate and apraclonidine hydrochloride have similarly been applied to the ocular mucosa to take advantage of their vasoconstrictive (and other) actions to treat ocular hypertension and open-angle glaucoma, also with great efficacy. However, drugs of these classes have never been used for topical application to the skin.

Although it was initially believed that their effects were modulated purely through their vasoconstrictive properties, it has been demonstrated in recent years that several of the {alpha}-adrenergic receptor vasoconstrictors also exhibit significant anti-inflammatory properties. In upper respiratory tract infections, oxymetazoline and xylometazoline have been shown to inhibit neutrophilic phagocytosis and oxidative burst, resulting in a decrease in microbial killing, decreased generation of proinflammatory cytokines, and decreased inflammation.16-17 Oxymetazoline has also recently been shown to have significant effects on the arachidonic acid cascade, strongly inhibiting 5-lipoxygenase activity and thus decreasing the synthesis of the highly proinflammatory leukotriene B4.17 A potential clinical role for oxymetazoline, or other agents of this class, as inhibitors of inflammation and oxidative-stress dependent reactions in inflammatory and/or infectious skin conditions is intriguing but has yet to be investigated.

Two major concerns of therapy with intranasal {alpha}-agonist decongestants are those of a loss of efficacy with prolonged use due to desensitization (tachyphylaxis) and rebound vasodilation with a flare of erythema and edema. Neither of our patients exhibited either problem with the application of oxymetazoline to the skin. While the laboratory induction of receptor desensitization cannot yet be perfectly correlated with actual physiologic response, recent laboratory studies indicate that agonists that are more selective for {alpha}1D-adrenoceptors are less prone to induce receptor desensitization than are {alpha}1A- or {alpha}1B-agonists.18 The clinical significance of this may be an important consideration in contemplating any potential future use of these drug classes on the skin because agonists with certain receptor subtype binding profiles may retain their clinically desirable effects while minimizing their adverse effect.

In these 2 patients with treatment-resistant ETR rosacea, we report that topically administering a selective {alpha}1-agonist has resulted in a positive clinical response. This was evidenced as a durable improvement in the erythema, a marked decrease of erythematous flares, relief from the symptoms of stinging and burning, and no adverse effects. It seems plausible that the erythema and flushing of ETR may be due, at least in part, to an abnormal expression, function, distribution, or responsiveness of {alpha}-adrenergic receptors, likely of an {alpha}1-receptor subtype, and that these clinical manifestations may be successfully treated by the topical application of agonists selective for {alpha}1-adrenergic receptors such as oxymetazoline.


AUTHOR INFORMATION


Correspondence: Stuart D. Shanler, MD, 100 Winston Dr, Apt 17E North, Cliffside Park, NJ 07010

Accepted for Publication: May 7, 2007.

Financial Disclosure: Drs Shanler and Ondo are principal owners and corporate officers in Aspect Pharmaceuticals LLC, Las Cruces, New Mexico, a privately held corporation that owns the rights to patent applications regarding the use of topically applied selective {alpha}1-agonists to the skin.


REFERENCES


1. Crawford GH, Pelle MT, James WD. Rosacea, I: etiology, pathogenesis, and subtype classification. J Am Acad Dermatol. 2004;51(3):327-341. FULL TEXT | ISI | PUBMED
2. Pelle MT, Crawford GH, James WD. Rosacea, II: therapy. J Am Acad Dermatol. 2004;51(4):499-512. FULL TEXT | ISI | PUBMED
3. Wilkin J, Dahl M, Detmer M, et al. Standard classification of rosacea: report of the National Rosacea Society Expert Committee on the classification and staging of rosacea. J Am Acad Dermatol. 2002;46(4):584-587. FULL TEXT | ISI | PUBMED
4. Plewig G, Kligman AM. Acne and Rosacea. 3rd ed. Berlin, Germany: Springer-Verlag; 2000:433-475.
5. Wilkin JK. Why is flushing limited to a mostly facial cutaneous distribution. J Am Acad Dermatol. 1988;19(2, pt 1):309-313. ISI | PUBMED
6. Wilkin JK. Oral thermal-induced flushing in erythematotelangiectatic rosacea. J Invest Dermatol. 1981;76(1):15-18. FULL TEXT | ISI | PUBMED
7. Parodi A, Guarrera M, Reboora A. Flushing in rosacea: an experimental approach. Arch Dermatol Res. 1980;269(3):269-273. FULL TEXT | ISI | PUBMED
8. Ahlquist RP. A study of the adrenotropic receptors. Am J Physiol. 1948;153:586-600. FREE FULL TEXT
9. Kirstein SL, Insel PA. Autonomic nervous system pharmacogenomics: a progress report. Pharmacol Rev. 2004;56(1):31-52. FREE FULL TEXT
10. Piascik MT, Perez DM. Alpha1-adrenergic receptors: new insights and directions. J Pharmacol Exp Ther. 2001;298(2):403-410. FREE FULL TEXT
11. Civantos Calzada B, Aleixandre de Artinano A. Alpha-adrenoceptor subtypes. Pharmacol Res. 2001;44(3):195-208. FULL TEXT | ISI | PUBMED
12. Guimarães S, Moura D. Vascular adrenoceptors: an update. Pharmacol Rev. 2001;53(2):319-356. FREE FULL TEXT
13. Hieble JP. Subclassification and nomenclature of alpha- and beta-adrenoceptors. Curr Top Med Chem. 2007;7(2):129-134. PUBMED
14. Jarajapu YP, Johnston F, Berry C, et al. Functional characterization of alpha1-adrenoceptor subtypes in human subcutaneous resistance arteries. J Pharmacol Exp Ther. 2001;299(2):729-734. FREE FULL TEXT
15. Leech CJ, Faber JE. Different alpha-adrenoceptor subtypes mediate constriction of arterioles and venules. Am J Physiol. 1996;270(2, pt 2):H710-H722. PUBMED
16. Bjerknes R, Steinsvag K. Inhibition of human neutrophil actin polymerization, phagocytosis, and oxidative burst by components of decongestive nose drops. Pharmacol Toxicol. 1993;73(1):41-45. ISI | PUBMED
17. Beck-Speier I, Dayal N, Karg E, et al. Oxymetazoline inhibits proinflammatory reactions: effect on arachidonic acid-derived metabolite. J Pharmacol Exp Ther. 2006;316(2):843-851. FREE FULL TEXT
18. Chalothorn D, McCune DF, Edelmann SE, et al. Differences in the cellular localization and agonist-mediated internalization properties of the alpha(1)-adrenoceptor subtypes. Mol Pharmacol. 2002;61(5):1008-1016.
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Re: "Afrin" cure?

Postby bentherebefore » Tue Nov 27, 2007 6:19 pm

Certainly worth the try, if done carefully.

This is my first day testing it on my face. I will buy different brands and try them out too. Right now I am applying with a soaked cotton ball of the stuff.

My immediate reaction... to me, it just feels like water on my face. No stinging or anything. Dries quickly. If I look really really close, I can see that it looks a little dry where I put it, but aloe vera does the exact same thing for me.
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Re: "Afrin" cure?

Postby Artist » Tue Nov 27, 2007 6:58 pm

I just squirted a little on my finger and spread it on my face over top my Emu oil after washing a little while ago. Just on the left side of my face. I'll report back on what happens. I've come a long way, but I'm still searching for the treatment that allows me to eat spicy food, aged cheese, and red wine. Maybe this will be the one. Here's hoping! :)

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Re: "Afrin" cure?

Postby sarah » Tue Nov 27, 2007 7:06 pm

Hi I am very interested in this and wondered if you could tell what i could use in the uk. I dont seem to be able to get afrin nasal drops here any alternatives you could suggest. Has anyone else tried it?
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Re: "Afrin" cure?

Postby Artist » Tue Nov 27, 2007 8:24 pm

I would just look for nasal sprays and eye drops with the active ingredient Oxymetazoline HCL. The concentration used in the study is .05%, so you may want to be sure you don't pick one with a higher concentration than that. I'm still very tentative about this. I have a hard time believing there would be no long-term rebound effects. I'll have to learn more about it. In the meantime, however, I'm comfortable trying it short term. Perhaps, if it helps, I could use it just on the weekends or on special occasions when I want to eat and drink and be merry (Santa)

Cheers!

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Re: "Afrin" cure?

Postby David Pascoe » Wed Nov 28, 2007 1:44 am

The study is encouraging that both of the participants didn't complain about rebound redness after quite a few months. Still, 2 is a very small number draw many conclusions from :shock: Those trying the competing Alphagan P all report some rebound redness, so IF this is already a better topical then that is great.

Usual disclaimer: I'll believe it when the FDA says so, yadda, yadda, yadda.
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Re: "Afrin" cure?

Postby Artist » Wed Nov 28, 2007 3:07 am

The Alphagen looks to be more of an Alpha 2 agonist. The Afrin is more of an Alpha 1 agonist. So, maybe that makes a difference. I'm not sure.. I do agree we should be cautious, though.

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Re: "Afrin" cure?

Postby Lisamouries » Wed Nov 28, 2007 12:56 pm


Perhaps, if it helps, I could use it just on the weekends or on special occasions when I want to eat and drink and be merry (Santa)



Oooooooooh that would be so excellent. I look forward to hear from your 'little' trial.
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Re: "Afrin" cure?

Postby Artist » Wed Nov 28, 2007 5:27 pm

David: Here they comment on why those two patients may not have experienced rebound.

"Two major concerns of therapy with intranasal {alpha}-agonist decongestants are those of a loss of efficacy with prolonged use due to desensitization (tachyphylaxis) and rebound vasodilation with a flare of erythema and edema. Neither of our patients exhibited either problem with the application of oxymetazoline to the skin.....................recent laboratory studies indicate that agonists that are more selective for {alpha}1D-adrenoceptors are less prone to induce receptor desensitization than are {alpha}1A- or {alpha}1B-agonists.18 The clinical significance of this may be an important consideration in contemplating any potential future use of these drug classes on the skin because agonists with certain receptor subtype binding profiles may retain their clinically desirable effects while minimizing their adverse effect."

I'm going to apply some again today. I applied it yesterday morning. I spent a lot of time on the computer and my skin heated up. When that happens, the pores on my cheeks expand a little and my skin doesn't look quite as smooth as usual. I was pleased to see it only happened on my untreated side. I did feel warmth over both cheeks, but the treated side looked perfectly smooth. The pores did not expand. Also, I had some slight sensitivity on my untreated side, but not the treated side. I had no issues with pinkness or redness or flushing yesterday, so I'm not sure about prevention of flushing/redness yet.

I'll report on how it goes today.


Cheers!

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Re: "Afrin" cure?

Postby bentherebefore » Wed Nov 28, 2007 6:40 pm

Well, I can say this already...

Vicks Sinex goes for about $5 at walmart. I opened it and it stinks... smells like Ben-Gay. Probably due to the menthol, and probably not too desirable for our skin or the smell..

The generic walmart Equate brand is 1.25 oz for about $2! No smell, goes on like water.

I'm going to try Afrin tomorrow to see how it goes. It goes for about $6 at walmart.
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