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Common and expected: Redness and flushing (2448 hours) Skin tightness and mild swelling Dryness and flaking (days 35) Temporary increased skin sensitivity Less common: Minor pinpoint bleeding during the procedure Mild bruising around sensitive zones Temporary breakout in acne-prone patients (due to increased skin activity) Stinging when applying skincare products in the first 48 hours Rare but possible: Post-inflammatory hyperpigmentation (PIH) is more likely in darker skin tones with improper technique or insufficient sun protection Infection extremely rare when proper sterilisation protocols are followed Cold sore flare-up in patients with a history of herpes simplex (antiviral prophylaxis may be recommended pre-treatment) If you notice increasing pain, any discharge or pus, or redness spreading well beyond the treated area in the days following your session, contact your clinic immediately
We hypothesised that the reported brainstem transcriptomic changes might reflect modulation of NTS Ppg neuron activity downstream of GIPR antagonism in the hypothalamus and therefore tested the effect of GIPR-antag on mice with ablated NTS Ppg neurons (Ppg NTS-Abl ) generated by bilateral stereotactic injection of AAV-DTA into the NTS of Ppg-Cre or control mice (Cre-negative mice receiving AAV-DTA into the NTS) (Fig
Alternate low-impact steady-state sessions to enhance fat oxidation with two weekly high-intensity-but-brief efforts to preserve metabolism
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