“…Studies of codeine, meperidine, and morphine indicate significantly more histamine release in vivo than with the newer semisynthetic opioids, fentanyl, sufentanil, and remifentanil [58,59,61,62]. A similar propensity for clinically significant histamine release has been observed for the older-generation muscle relaxants (e.g., mivacurium, tubocurarine, and atracurium) compared with newer products, for example vecuronium and cisatracurium, when administered in standard clinical doses [48,[63][64][65][66][67]. Furthermore, a drug's basic (versus acidic) character may affect mast cell activation, because positively-charged cations, for example narcotics and muscle relaxants, are believed to be involved in mast cell activation via non-receptor-mediated G-protein activation [9,11,65,66].…”