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Atypical Growth Hormone Releasing Peptidesachievement. Their artificiality was underscored by the fact that they were invented rather than isolated (1, 2). This conclusion was reinforced when it became increasingly apparent that the GHRPs did not release GH via the GHRH receptor and acted via different endocrine and molecular mechanisms tha
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https://doi.org/10.1007/978-1-4899-3776-6ypes will not be discussed unless directly relevant to ionic mechanisms in somatotrophs. We will begin by summarizing the ionic mechanisms by which . (GRF) stimulates the acute release of GH via . (cAMP) and cytosolic free Ca. ([Ca.].) as second messengers (Fig. 2.1). This is discussed in more detail elsewhere in this volume.
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Transmission and Movement of Plant Viruses,it became increasingly apparent that the GHRPs did not release GH via the GHRH receptor and acted via different endocrine and molecular mechanisms than GHRH to release GH (3–18). Subsequently, however, this more technical viewpoint of the GHRPs has gradually changed.
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Plant Tissue Culture Manual - Supplement 5(7, 8). Furthermore, in the striatum, where it has been implicated in modulating locomotor activity (9, 10), SRIF is a major stimulant of dopamine release from nigrostriatal neurons and may interact with dopamine in modulating basal ganglia functions (11).
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Plant Tissue Culture: An Introductory Texte. GHRH and SRIF act out of phase to stimulate or suppress GH secretion, respectively. Peripheral hormones, including steroid and thyroid hormones as well as . (IGF-I) and . (IGF-II), also participate in the control of GH secretion.
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M. S. Parvathi,Karaba N. Nataraja immune system (4). Thus, the evidence taken together supports the existence of the same signal molecules and receptors that potentially mediate interactions both between and within the neuroendocrine and immune systems.
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Biochemical and Functional Properties of Somatostatin Receptors(7, 8). Furthermore, in the striatum, where it has been implicated in modulating locomotor activity (9, 10), SRIF is a major stimulant of dopamine release from nigrostriatal neurons and may interact with dopamine in modulating basal ganglia functions (11).
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