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Susan Kralisch University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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Johannes Klein University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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Ulrike Lossner University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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Matthias Bluher University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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Ralf Paschke University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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Michael Stumvoll University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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Mathias Fasshauer University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany
University of Lübeck, Department of Internal Medicine I, 23538 Lübeck, Germany

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a cellular increase in cAMP concentrations would be sufficient to downregulate visfatin mRNA. Cholera toxin activates G S -proteins by ADP-ribosylation whereas forskolin is a direct activator of adenylyl cyclase. 3T3-L1 adipocytes were treated with

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Mark E Peterson Animal Endocrine Clinic, Department of Clinical Sciences, 21 West 100th Street, New York, New York 10025, USA
Animal Endocrine Clinic, Department of Clinical Sciences, 21 West 100th Street, New York, New York 10025, USA

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subgroups regulate adenylyl cyclase activity, which in turn controls the formation of cAMP ( Wettschureck & Offermanns 2005 ). The G s proteins are stimulatory to adenylyl cyclase, while the G i proteins are inhibitory. Adenylyl cyclase activity and cAMP

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Maria Esteban-Lopez Department of Human and Molecular Genetics, Herbert Wertheim College of Medicine, Miami, Florida, USA

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Alexander I Agoulnik Department of Human and Molecular Genetics, Herbert Wertheim College of Medicine, Miami, Florida, USA
Biomolecular Science Institute, Florida International University, Miami, Florida, USA

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done to further characterize INSL3/RXFP2 signaling and functions. Mechanisms of INSL3 binding and activation of RXFP2 INSL3 treatment of HEK293T cells transfected with RXFP2 causes activation of the classical adenylyl cyclase (AC) pathway via

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Lucia Zhang Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada

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Kathy K Lee Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada

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Kim S Sugamori Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada

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Marc D Grynpas Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada

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Jane Mitchell Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada

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). Gα S , encoded by the GNAS gene located on human chromosome 20 ( Gnas on chromosome 2 in mice), is widely expressed and known for its activation of adenylyl cyclases to generate cAMP with a myriad of effects on cell metabolism and gene expression

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Toshio Shimada Department of Physiology, Nagasaki University School of Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto-machi, Nagasaki 852-8523, Japan

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Taeko Hirose Department of Physiology, Nagasaki University School of Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto-machi, Nagasaki 852-8523, Japan

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Itsuro Matsumoto Department of Physiology, Nagasaki University School of Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto-machi, Nagasaki 852-8523, Japan

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Tadaomi Aikawa Department of Physiology, Nagasaki University School of Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto-machi, Nagasaki 852-8523, Japan

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, leading to the simultaneous stimulation of distinct signaling pathways. While the ACTH receptor interacts preferentially with stimulatory G-protein (G s ) to stimulate adenylyl cyclase (AC), coupling to inhibitory G-protein (G i ) has also been reported

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Helen L Henderson Department of Anatomy, University of Bristol, Bristol BS2 8EJ, England, UK

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Julie Townsend Department of Anatomy, University of Bristol, Bristol BS2 8EJ, England, UK

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Domingo J Tortonese Department of Anatomy, University of Bristol, Bristol BS2 8EJ, England, UK

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pathway responsible for reduced gene transcription following activation of the dopamine receptor results in the inhibition of adenylyl cyclase ( Taussig & Gilman 1995 ), decrease in cAMP production and suppression of activated PKA ( Diamond et al . 1999

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Deborah P Fischer
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Jonathon A Hutchinson
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Diane Farrar School of Pharmacy, Bradford Royal Infirmary, Department of Biological Sciences, University of Bradford, West Yorkshire BD7 1DP, UK

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Peter J O'Donovan School of Pharmacy, Bradford Royal Infirmary, Department of Biological Sciences, University of Bradford, West Yorkshire BD7 1DP, UK

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David F Woodward School of Pharmacy, Bradford Royal Infirmary, Department of Biological Sciences, University of Bradford, West Yorkshire BD7 1DP, UK

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Kay M Marshall
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-coupled DP, EP 2 , EP 4 and IP receptors mediate uterine relaxation via adenylyl cyclase and cyclic AMP (cAMP). By contrast, activation of EP 1 , EP 3 , FP and TP receptors by uterotonins either reduces intracellular cAMP or mobilises calcium to facilitate

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Christopher J Charles
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Takeshi Katafuchi Christchurch Cardioendocrine Research Group, National Cardiovascular Center Research Institute, University of Otago Christchurch, Christchurch 8140, New Zealand

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Timothy G Yandle
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Naoto Minamino Christchurch Cardioendocrine Research Group, National Cardiovascular Center Research Institute, University of Otago Christchurch, Christchurch 8140, New Zealand

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strong affinity to porcine CRSP-1 and mediates its signal into cells by activating adenylyl cyclase. Porcine CT-R was transiently expressed in COS-7 cells, and then those cells were stimulated with ovine/caprine CRSP-1 or caprine CRSP-2 and compared with

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Araceli Morales Laboratory of Cellular Neurobiology, Department of Physiology and
Laboratory of Animal Physiology, Department of Animal Biology, Institute of Biomedical Technologies, University of La Laguna, La Laguna, Spain

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Miriam Gonzalez Laboratory of Cellular Neurobiology, Department of Physiology and
Laboratory of Animal Physiology, Department of Animal Biology, Institute of Biomedical Technologies, University of La Laguna, La Laguna, Spain

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Raquel Marin Laboratory of Cellular Neurobiology, Department of Physiology and
Laboratory of Animal Physiology, Department of Animal Biology, Institute of Biomedical Technologies, University of La Laguna, La Laguna, Spain

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Mario Diaz Laboratory of Cellular Neurobiology, Department of Physiology and
Laboratory of Animal Physiology, Department of Animal Biology, Institute of Biomedical Technologies, University of La Laguna, La Laguna, Spain

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Rafael Alonso Laboratory of Cellular Neurobiology, Department of Physiology and
Laboratory of Animal Physiology, Department of Animal Biology, Institute of Biomedical Technologies, University of La Laguna, La Laguna, Spain

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-epinephrine (NE), and that this effect was apparently exerted at a level upstream adenylyl cyclase (AC; Martinez-Morales et al. 2001 ). In the present work, we have investigated whether this modulatory effect can be exerted through estrogen interactions with

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K K Sidhu Department of Endocrinology, Barts and the Royal London School of Medicine and Dentistry, West Smithfield, London EC1A 7BE, UK
Veterinary Basic Sciences, Royal Veterinary College, Royal College Street, London NW1 0TU, UK

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R C Fowkes Department of Endocrinology, Barts and the Royal London School of Medicine and Dentistry, West Smithfield, London EC1A 7BE, UK
Veterinary Basic Sciences, Royal Veterinary College, Royal College Street, London NW1 0TU, UK

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R H Skelly Department of Endocrinology, Barts and the Royal London School of Medicine and Dentistry, West Smithfield, London EC1A 7BE, UK
Veterinary Basic Sciences, Royal Veterinary College, Royal College Street, London NW1 0TU, UK

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J M Burrin Department of Endocrinology, Barts and the Royal London School of Medicine and Dentistry, West Smithfield, London EC1A 7BE, UK
Veterinary Basic Sciences, Royal Veterinary College, Royal College Street, London NW1 0TU, UK

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receptors in the neurointermediate lobe: lack of coupling to either stimulation or inhibition of adenylyl cyclase. Endocrinology 141 1301 –1309. Wheeler MB , Lu M, Dillon JS, Leng X-H, Chen C & Boyd AE 1993 Functional

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