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| weight loss zonisamide |
weight loss zonisamide
Zonisamide is a unique drug that affects the excitatory neurotransmitter glutamate, thereby causing a reduction in the glutamatergic transmission of input from the sensory cortex. This results in decreased neuronal activity and an initial reduction in food intake, which is maintained by a reduction in the number of eating episodes.
With the advent of alternative medications, people are increasingly turning to the use of natural products. For example, in the United States alone, about 9 out of 10 Americans use natural products, and more than 200 million Americans use herbal products. Amongst people who are using herbal products, it is estimated that 20% are looking for natural weight loss products. In this case study, we are going to review the herbal weight loss product, zeolite.
Zonisamide is a novel anticonvulsant drug whose pharmacological activity was first described in the early 1980s. It inhibits GABAergic transmission by a competitive but non-selective action as an antagonist at the [4-aminopyridine (4-AP)-sensitive] (GABA-A) channel, with a high affinity for the alpha4 subunit and also a lesser affinity for alpha2 and alpha3 subunits. It has also been suggested that zonisamide may modulate AMPA-mediated responses, but the precise mechanism of this action is unknown, though it may involve ion channel inhibition or modulation of the activity of second-messenger dependent intracellular protein(s) such as Ca2+, calmed
Zonisamide, or (RS)-5-hydroxy-1-(4-oxo-2-thiazolyl)benzimidazole-2-sulfonamide, is a sulfamoylbenzoate derivative of a benzimidazole. The medication is used for the treatment of epilepsy and depression. Zonisamide has neuroprotective and anticonvulsant properties in preclinical models. Zonisamide also exhibits neuroregenerativie
Zonisamide is a medication used for the treatment of partial seizures and generalized tonic-clonic seizures. Zonisamide is a benzisoxazole derivative of zonisamide, a substance derived from the fungus (Bolton, 1997). Zonisamide has been in human clinical trials since the 1990s.
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