Topical minoxidil counteracts stress-induced hair growth inhibition in mice

:  Stress has long been suspected as a possible cause of hair loss in various species, even though convincing experimental evidence has not been available. Recently, we have shown in a murine model that sonic stress alters hair growth and cycling in vivo, and have postulated the existence of a ‘brai...

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Veröffentlicht in:Experimental dermatology 2003-10, Vol.12 (5), p.580-590
Hauptverfasser: Arck, Petra Clara, Handjiski, Bori, Peters, Eva M. J., Hagen, Evelin, Klapp, Burghard F., Paus, Ralf
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container_end_page 590
container_issue 5
container_start_page 580
container_title Experimental dermatology
container_volume 12
creator Arck, Petra Clara
Handjiski, Bori
Peters, Eva M. J.
Hagen, Evelin
Klapp, Burghard F.
Paus, Ralf
description :  Stress has long been suspected as a possible cause of hair loss in various species, even though convincing experimental evidence has not been available. Recently, we have shown in a murine model that sonic stress alters hair growth and cycling in vivo, and have postulated the existence of a ‘brain‐hair follicle axis’ (BHA). In order to study whether a clinically available and widely used topically active hair growth stimulator mitigates stress‐triggered hair growth inhibition in this stress model, we have applied a 5% minoxidil solution. Female CBA/J mice were depilated and randomized in to two groups: control (n = 20) and sonic stress (n = 20). These groups were further divided and either treated daily with 5% minoxidil solution or vehicle alone. The stress group was exposed to sonic stress for 24 h starting 14 days after anagen induction by depilation. All mice were sacrificed 16 days after the depilation and assessed by quantitative histomorphometry. Sonic stress significantly increased the number of hair follicles with apoptotic cells and inhibited intrafollicular keratinocyte proliferation. In addition, the number of clusters of perifollicular MHC class II+ cells and degranulated perifollicular mast cells was significantly enhanced in the stressed mice. In accordance with previous findings, all stressed mice showed an advanced hair cycle progression towards catagen. All of these stress‐induced hair growth inhibitory changes along the BHA were down‐regulated by topical minoxidil application. This encourages one to explore clinically whether topical minoxidil is a safe and effective pharmacologic tool for the management of stress‐associated telogen effluvium in humans.
doi_str_mv 10.1034/j.1600-0625.2003.00028.x
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The stress group was exposed to sonic stress for 24 h starting 14 days after anagen induction by depilation. All mice were sacrificed 16 days after the depilation and assessed by quantitative histomorphometry. Sonic stress significantly increased the number of hair follicles with apoptotic cells and inhibited intrafollicular keratinocyte proliferation. In addition, the number of clusters of perifollicular MHC class II+ cells and degranulated perifollicular mast cells was significantly enhanced in the stressed mice. In accordance with previous findings, all stressed mice showed an advanced hair cycle progression towards catagen. All of these stress‐induced hair growth inhibitory changes along the BHA were down‐regulated by topical minoxidil application. 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J.</creatorcontrib><creatorcontrib>Hagen, Evelin</creatorcontrib><creatorcontrib>Klapp, Burghard F.</creatorcontrib><creatorcontrib>Paus, Ralf</creatorcontrib><title>Topical minoxidil counteracts stress-induced hair growth inhibition in mice</title><title>Experimental dermatology</title><addtitle>Exp Dermatol</addtitle><description>:  Stress has long been suspected as a possible cause of hair loss in various species, even though convincing experimental evidence has not been available. Recently, we have shown in a murine model that sonic stress alters hair growth and cycling in vivo, and have postulated the existence of a ‘brain‐hair follicle axis’ (BHA). In order to study whether a clinically available and widely used topically active hair growth stimulator mitigates stress‐triggered hair growth inhibition in this stress model, we have applied a 5% minoxidil solution. Female CBA/J mice were depilated and randomized in to two groups: control (n = 20) and sonic stress (n = 20). These groups were further divided and either treated daily with 5% minoxidil solution or vehicle alone. The stress group was exposed to sonic stress for 24 h starting 14 days after anagen induction by depilation. All mice were sacrificed 16 days after the depilation and assessed by quantitative histomorphometry. Sonic stress significantly increased the number of hair follicles with apoptotic cells and inhibited intrafollicular keratinocyte proliferation. In addition, the number of clusters of perifollicular MHC class II+ cells and degranulated perifollicular mast cells was significantly enhanced in the stressed mice. In accordance with previous findings, all stressed mice showed an advanced hair cycle progression towards catagen. All of these stress‐induced hair growth inhibitory changes along the BHA were down‐regulated by topical minoxidil application. 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Drug treatments</subject><subject>Skin, nail, hair, dermoskeleton</subject><subject>sonic stress</subject><subject>Stress, Physiological - complications</subject><subject>Stress, Physiological - physiopathology</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9P2zAYh61p09oxvsKUC7slvPF_S7sgVgqsggsTvVmO46zu0qTYiQjffgmt4LqTLb_P77XfxwglOWQ5EHq-zXIOkALHLMMAJAMALLPhA5q_FT6iOSjgKRfAZuhLjFuAXBDBPqNZTsdDoeQc_Xpo996aOtn5ph186evEtn3TuWBsF5PYBRdj6puyt65MNsaH5E9on7tN4puNL3zn22bcjnHrvqJPlamjOz2uJ-j31eLh8jpd3S9vLi9WqaUEy5RAaUVZYQeiNKQsFKm4M1RazBWw3CpMOTAGxhEuuMLSQiE4NQCFlFJJcoK-H_ruQ_vUu9jpnY_W1bVpXNtHLXKqqMATKA-gDW2MwVV6H_zOhBedg55E6q2efOnJl55E6leRehij34539MXOle_Bo7kRODsCJo7-qmAa6-M7x8bGVLGR-3Hgnn3tXv77AXqx_gmvI6SHuI-dG97iJvzVfPpM_Xi31Gx9JdYAS31L_gGk_pyk</recordid><startdate>200310</startdate><enddate>200310</enddate><creator>Arck, Petra Clara</creator><creator>Handjiski, Bori</creator><creator>Peters, Eva M. 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J. ; Hagen, Evelin ; Klapp, Burghard F. ; Paus, Ralf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4328-30dc7df2e07da3db93f6ea48c269051c92460550ae3676928c0b764a00b888983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Alopecia - etiology</topic><topic>Alopecia - prevention &amp; control</topic><topic>Animals</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biological and medical sciences</topic><topic>Cell Degranulation</topic><topic>Cell Division - drug effects</topic><topic>Female</topic><topic>Hair Follicle - cytology</topic><topic>Hair Follicle - drug effects</topic><topic>Hair Follicle - growth &amp; development</topic><topic>hair growth inhibition</topic><topic>mast cells</topic><topic>Mast Cells - physiology</topic><topic>Medical sciences</topic><topic>MHC II + cells</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>Minoxidil - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Skin, nail, hair, dermoskeleton</topic><topic>sonic stress</topic><topic>Stress, Physiological - complications</topic><topic>Stress, Physiological - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arck, Petra Clara</creatorcontrib><creatorcontrib>Handjiski, Bori</creatorcontrib><creatorcontrib>Peters, Eva M. 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In order to study whether a clinically available and widely used topically active hair growth stimulator mitigates stress‐triggered hair growth inhibition in this stress model, we have applied a 5% minoxidil solution. Female CBA/J mice were depilated and randomized in to two groups: control (n = 20) and sonic stress (n = 20). These groups were further divided and either treated daily with 5% minoxidil solution or vehicle alone. The stress group was exposed to sonic stress for 24 h starting 14 days after anagen induction by depilation. All mice were sacrificed 16 days after the depilation and assessed by quantitative histomorphometry. Sonic stress significantly increased the number of hair follicles with apoptotic cells and inhibited intrafollicular keratinocyte proliferation. In addition, the number of clusters of perifollicular MHC class II+ cells and degranulated perifollicular mast cells was significantly enhanced in the stressed mice. In accordance with previous findings, all stressed mice showed an advanced hair cycle progression towards catagen. All of these stress‐induced hair growth inhibitory changes along the BHA were down‐regulated by topical minoxidil application. This encourages one to explore clinically whether topical minoxidil is a safe and effective pharmacologic tool for the management of stress‐associated telogen effluvium in humans.</abstract><cop>Oxford, UK</cop><pub>Munksgaard International Publishers</pub><pmid>14705798</pmid><doi>10.1034/j.1600-0625.2003.00028.x</doi><tpages>11</tpages></addata></record>
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subjects Alopecia - etiology
Alopecia - prevention & control
Animals
apoptosis
Apoptosis - drug effects
Biological and medical sciences
Cell Degranulation
Cell Division - drug effects
Female
Hair Follicle - cytology
Hair Follicle - drug effects
Hair Follicle - growth & development
hair growth inhibition
mast cells
Mast Cells - physiology
Medical sciences
MHC II + cells
Mice
Mice, Inbred CBA
Minoxidil - pharmacology
Pharmacology. Drug treatments
Skin, nail, hair, dermoskeleton
sonic stress
Stress, Physiological - complications
Stress, Physiological - physiopathology
title Topical minoxidil counteracts stress-induced hair growth inhibition in mice
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