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skintegral® Natural Compound Research

Major Focus:

Research activities of skintegral™ are dedicated to investigating beneficial effect of plant extracts, minerals and solar light on the skin. Plant extracts contain a variety of natural compounds with therapeutic relevance, such as free radical scavenging, anti-inflammatory and antimicrobial effects. The dermatologic usability of most of these compounds is only partly explored.

Prof.Christoph M.Schmepp, MD, PhD

Biologist, Dermatologist

 

Phone: + 49 (0)761 270-67010

christoph.schempp@uniklinik-freiburg.de

ORCID: 0000-0002-1372-998X

CV

Current position

Head of the photodermatology unit, head of the inpatient department - focus inflammation, head of the research centre skintegral

2005

Appointed Professor of Dermatology, University of Freiburg

2000

Certificate in allergologie in dermatology and allergologie, University of Freiburg

1994

State examination in medicine, MD doctoral thesis in dermatology, Free University of Berlin, Germany

1987

PhD degree in biology and pharmacy, University of Tübingen, Germany

Prof.Ute Wölfle, PhD

Biologist, Dermatologist

 

Phone: + 49 (0)761 270-68250

E-Mail:

ORCID: 0000-0003-0093-560X

CV

Current position (2008 ongoing)

Postdoctoral studies, since 2015 lab leader at the research group skintegral, Department of Dermatology, University Medical Center Freiburg

2023

Appointed Professor of Experimental Dermatology, University of Freiburg

2006-2007

Product Scientist at the Life Science Group of Sysmex, Norderstedt, Germany

1999-2006

PhD dissertation and 3 year postdoctoral studies at the Institute of Tumor Biology, UKE Hamburg, Head: Prof. Klaus Pantel

1993-1999

Biological studies at the university of Freiburg and performing the Diploma thesis at the Max Planck Institute for Immunology, Freiburg, Group Leader: Prof. Dr. Ursula Klingmüller,

Team

Doctoral/Master students

 

Zita Hurth (cand. MD)

 

Marie-Luise Faber (cand. MD)

 

Technician

 

Birgit Haarhaus, MTA

 

Alumni

 

2025

Christina Maria Sager

2024

Maximilian Becker

2024

Lucia Ratzke

2020

Natalja Weber

2019

Deborah Gregersen

2018

Jasmin Seiwerth

2017

Lea Zimmermann

2017

Georgia Tasiopoulou

Key Puclications

2022

Hurth Z, Faber ML, Gendrisch F, Holzer M, Haarhaus B, Cawelius A, Schwabe K, Schempp CM, Wölfle U. The Anti-Inflammatory Effect of Humulus lupulus Extract In Vivo Depends on the Galenic System of the Topical Formulation. Pharmaceuticals. 2022, doi: 10.3390/ph15030350

2018

Kapp, F.G., Perlin, J.R., Hagedorn, E.J., Gansner, J.M., Schwarz, D.E., O’Connell, L.A., Johnson, N.S., Amemiya, C., Fisher, D.E., Wölfle, U., Trompouki, E., Niemeyer, C.M., Driever, W., Zon, L.I., 2018. Protection from UV light is an evolutionarily conserved feature of the haematopoietic niche. Nature. 2018, doi: 10.1038/s41586-018-0213-0

2015

Wölfle, U., Elsholz, F.A., Kersten, A., Haarhaus, B., Müller, W.E., Schempp, C.M., 2015. Expression and functional activity of the bitter taste receptors TAS2R1 and TAS2R38 in human keratinocytes. Skin Pharmacology and Physiology. 2015, doi: 10.1159/000367631

2015

Wölfle, U., Haarhaus, B., Schempp, C.M., 2015c. Amarogentin Displays Immunomodulatory Effects in Human Mast Cells and Keratinocytes. Mediators Inflamm. 2015, doi: 10.1155/2015/630128

2011

Wölfle, U., Esser, P.R., Simon-Haarhaus, B., Martin, S.F., Lademann, J., Schempp, C.M., 2011. UVB-induced DNA damage, generation of reactive oxygen species, and inflammation are effectively attenuated by the flavonoid luteolin in vitro and in vivo. Free Radical Biology and Medicine. 2011, doi:10.1016/j.freeradbiomed.2011.01.027

Funding

Wilhelm Doerenkamp Foundation, Sanddorf Foundation and Software AG Foundation, Christophorus Foundation, DAMUS-DONATA e.V., Dr. Hauschka Foundation, Mahle Foundation, Rudolf Steiner Fund

Background

Research projects

Influencing the interaction of psoriasis keratinocytes and fatty liver cells by liver remedies of the integrative medicine (PSORI-HEP study)

Funded by the Sanddorf Foundation and Software AG Foundation

 

Psoriasis is a noncommunicable, partly genetically determined, chronic inflammatory skin disease associated with several comorbidities. One of the most common comorbiditiy is the metabolic syndrome that include obesity, diabetes mellitus, elevated liver enzymes and : Metabolic dysfunction-associated fatty liver disease (MAFLD). The research project  investigates  the association of psoriasis with MAFLD using several experimental models. The main question is whether treatment of fatty liver cells with liver therapeutics or complex gastrointestinal-liver-bile remedies can improve the expression of psoriasis inflammation.

Network between adipose tissue, liver and skin (modified from Mantovani et al. IJMS 2016; Heitmann et al. JDDG, 2021)

MAFLD: metabolic dysfunction-associated fatty liver disease; MASH: metabolic dysfunction-associated steatohepatitis

Antimonite crystal (Photo: State Museum of Natural History Karlsruhe)

Antimony (Stibium, Sb) and Antimonite (Stibnite, Sb2S3) are metalloids with anti-infective and immunosuppressive properties. They have been used as remedies for a long time, but in recent times they are only used restrictively to treat certain parasitoses due to their toxicity. Antimony and antimonite are also used in anthroposophic medicine in diluted nontoxic preparations. In this research project, dose-response relationships and active principles of antimony, antimonite and the antimony compound Tartarus stibiatus were investigated on psoriasis-like keratinocytes. It was shown that antimony / antimonite - but especially Tartarus stibiatus - causes a reduction in keratinocyte proliferation and a reduction in psoriatic inflammation. 

Effect of botanical compounds on psoriasis keratinocytes in vitro and in vivo

Funded by the Wilhelm Doerenkamp Foundation, Chur (Switzerland)

In this project, the anti-psoriatic effect of traditionally used and novel botanical compounds was investigated. Of particular interest are active plant compounds from Centella asiatica (asiatic pennywort with madecassoids and asiaticosides), Mahonia aquifolium (mahonia with berberine), Curcuma amada (mango ginger with the diterpenoid LDD) and Whrightia tinctoria (sweet indraja with triterpenes and sterols), as they have been used in Ayurvedic and traditional Chinese medicine for thousands of years to treat skin diseases. In addition, the traditional medicinal plants from occidental monastic medicine Hypericum perforatum (St. John's wort with hyperforin) and Humulus lupulus (hops with humulone and lupulone) could be effective. After screening the botanical compounds for anti-inflammatory and anti-proliferative effects, hops and St. John's wort were found to be particularly promising botanical compounds in psoriasis models in vitro and ex vivo.

Physiological role of bitter taste receptors in the skin

In recent years, it has been discovered that certain taste receptors, the bitter taste receptors (TAS2Rs), are not only present on the tongue and upper gastrointestinal tract, but also on the bronchi of the lung. The binding of bitter substances to TA2Rs in the lung induces bronchodilation. This may be of therapeutic use in the treatment of asthma bronchiale. The research unit skintegral could show that the skin also possesses bitter taste receptors.   

Plant derived bitter agents from gentian (amarogentin) or willow bark (salicin) bind to these bitter taste receptors and induce calcium influx into keratinocytes. This leads to the synthesis of lipids and proteins that are crucial for the formation of the skin barrier (e.g. keratins, filaggrin). Bitter substances thus stimulate the skin's metabolism. In addition, they have anti-allergic effects.

Method spectrum

The efficacy and skin tolerability of natural compounds in topical preparations depends on the liberation and penetration of the compounds from the vehicle, a scientific field covered by dermopharmacy. Natural substances used in dermatology should not have any sensitizing or phototoxic potential. To address this, various cell culture models and molecular methods are established in our laboratory. Clinically, the substances are investigated in skin tests such as the patch test or the ultraviolet erythema test. The spectrum of methods includes bioengeneering methods such as the measurement of skin hydration, transepidermal water loss, skin perfusion and sebumetry.

Cooperations

The integrative approach of our research area is highlighted by interdisciplinary research projects with phytotherapy, allergology, biology, pharmacy and complementary medicine. 

In particular, there are collaborations with:

  • Prof. Dr. rer. nat. Stefan Martin und Dr. rer. nat. Philipp Esser, Allergy Research Group (ARG), University Medical Center, Freiburg

  • Prof. Dr. med Tobias Böttler; Dr. Giuseppe Rusignuolo, Department of Medicine II, University Medical Center, Freiburg 

  • Dr. rer. nat. Karl Quirin und Anja Cawelius, Naturextrakte GmbH, Rehlingen

  • Prof. Dr. med. Roman Huber, Center for Complementary Medicine, University Medical Center, Freiburg

  • PD Dr. Dr. rer. nat. Franck A. Ditengou , Bio Imaging Core Light Microscopy (BiMiC), University Medical Center Freiburg

  • Prof. Dr. rer. nat. Kateřina Vávrová, Faculty of Pharmacy Hradec Kralove, Charles University, CZE

  • Dr. rer. nat. Martin Holzer Department of Pharmaceutical Technology and Biopharmacy, University Freiburg 

  • Prof. Dr. rer. nat. Ralf Weißenkirchen, Institute of Molecular Pathobiochemistry, RWTH University Hospital Aachen

  • Prof. Dr. med Martin Wabitsch, Division of Paediatric Endocrinology and Diabetes, University Medical Centre, Ulm

  • Dr. rer. nat. Kay Schwabe, Beauty Science Intelligent GmbH, Langenhagen

  • Prof. Dr. Dr.-Ing. Jürgen Lademann und Prof. Dr. rer. nat. Martina Meinke, Center of Experimental and Applied Cutaneaous Physiology, Charité Berlin