Rats: To investigate the inducer activity on erection, melanotan (MT)-II or vehicle (saline) is acutely injected i.v., i.t. or within the PVN after a 5 min baseline recording period is obtained. ICP and MAP are then recorded for a 60 min period after saline or melanotan (MT)-II delivery. I.v. injections (three doses; 0.1, 0.3, and 1 mg/kg in saline) are performed with a catheter inserted in the jugular vein[2].
Mice: Melanotan (MT)-II (0.1 and 0.2 nM) or vehicle (artificial cerebrospinal fluid) is administered. SPA is recorded continuously every 5 min. Food intake measurements are taken 6 and 24 h postinjection. Body weight is measured every 24 h. Chow and water are available ad libitum. A 48-h interval occurrs between drug treatments[5].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Custom Peptide Synthesis Melanotan (MT)-II Chemical Structure CAS No. : 121062-08-6 SizePriceStockQuantity 1 mg ￥800 In-stock 5 mg ￥1600 In-st...Melanotan (MT)-II | Others | Inhibitor | inhibitor | inhibitMelanotan (MT)-II是一种合成的黑皮质素 (melanocortin) 受体激动剂。它是可注射用的多肽荷尔蒙，可促进晒黑。- 高纯度，全球文献引用。Melanotan (MT)
本文链接： http://mtpeptide.immuno-online.com/view-773703.html
