In vascular smooth muscle, cyclic nucleotide-dependent phosphorylation of heat shock protein 20 (HSP20) on ser¹⁶ has been suggested to cause force suppression, i.e., reduced force with only minimal myosin regulatory light chain (MRLC) dephosphorylation. We hypothesized that heat pretreatment also suppresses force by increasing HSP20 phosphorylation. After heat pretreatment of swine carotid artery at 44.5°C for 4 hours and reduction to 37°C for 1 hour, ser¹⁶-HSP20 phosphorylation was increased and histamine-induced increases in contractile force were suppressed. Subsequent addition of nitroglycerin induced additive force suppression. Heat and nitroglycerin induced a similar relation between ser¹⁶-HSP20 phosphorylation and force. Heat pretreatment induced a small, but significant increase in total HSP20 immunostaining. These results demonstrate that vascular smooth muscle responds to thermal stress by increasing ser¹⁶-HSP20 phosphorylation in addition to a possible small increase in total [HSP20]. The resulting heat-induced reduction in force should be considered "force suppression" since histamine induced increases in MRLC phosphorylation were not significantly altered by heat pretreatment. These processes may bring about a resistance to contractile agonists, which could have clinical significance in conditions such as hyperthermia, and/or sepsis with vasodilatory shock.